..
Suche
Hinweise zum Einsatz der Google Suche
Erweiterte Suche
Personensuchezur unisono Personensuche
Veranstaltungssuchezur unisono Veranstaltungssuche
Katalog plus

Publications

2023, 2022, 2021, 2020, 2019, 2018, 2017, 2016, 2015, 2014, 2013, 2012, 2011, 2010, 2009, 2008, 2007, 2006, 2005, 2004, 2003,

2002, 2001, 2000, 1999, 1998, 1997, 1996, 1995, 1994, 1993, 1992, 1991, 1990, 1989, 1988, 1987, 1986, 1985, 1984, 1983, 1982,

1981

Statistik

  
 
 

 

2023 ↑

  
336

E. Elramadi, S. Kundu, D. Mondal, M. Schmittel,
Concurrent tandem catalysis enabled by nanomechanical motion in heteroleptic four-component dual-catalyst machinery,
Chem. Commun. 2023, 59, 4915 – 4918.
DOI: dx.doi.org/10.1039/d3cc00637a

 

335

D. Mondal, S. Kundu, E. Elramadi, I. Valiyev, M. Schmittel,
Self-healing of a Copper(I) [2]Rotaxane Shuttle Monitored by Fluorescence,
Org. Lett. 2023, 25(6), 933–937.
DOI: dx.doi.org/10.1021/acs.orglett.2c04237

 

334

S. Kundu, I. Valiyev, D. Mondal, V. Rajasekaran, A. Goswami, M. Schmittel,
Proton transfer network with luminescence display controls OFF/ON catalysis that generates a high-speed slider-on-deck,
RSC Advances, 2023, 13, 5168–5171.
DOI: dx.doi.org/10.1039/d3ra00062a

 

 


2022     ↑

333

S. Kundu, D. Mondal, V. Rajasekaran, A. Goswami, M. Schmittel,
Three-Input Logic AND Gate Drives Sequential Three-Step Catalysis by Parallel Activation of Catalyst Duo,
Inorg. Chem. 2022, 61, 17007−17011.
DOI: dx.doi.org/10.1021/acs.inorgchem.2c03349

 

332

S. Saha, S. Kundu, P. K. Biswas, M. Bolte, M. Schmittel,
Dynamics of the alkyne→copper(I) interaction and its use in a heteroleptic four-component catalytic rotor,
Chem. Commun. 2022, 58, 13019–13022.
DOI: dx.doi.org/10.1039/d2cc04497h

 

331

A. Bielecki, M. Schmittel,
The information encoded in structures: theory and application to molecular cybernetics,
Foundations of Science, 2022, 27, 1327-1345.
https://doi.org/10.1007/s10699-022-09830-8

 

330

V. V. Rajasekaran, A. Ghosh, S. Kundu, D. Mondal, T. Paululat, M. Schmittel,
Synchronizing Two Distinct Nano-Circular Sliding Motions in Six-Component Machinery for Dual Catalysis,
Angew. Chem. Int. Ed. 2022, 61, e202212473.
DOI: dx.doi.org/10.1002/anie.202212473
Angew. Chem. 2022, 61, e202212473.
DOI: dx.doi.org/10.1002/ange.202212473

 

329

A. Badami-Behjat, P. Deimel, F. Allegretti, E. Ringel, K. Mahata, M. Schmittel, J. Barth, W. Heckl, M. Lackinger,
Versatile role of molecule-surface interactions for monolayer self-assembly at liquid-solid interfaces: substrate-induced polymorphism, thermodynamic stability and new polymorphs,
Chem. Mat. 2022, 34, 8876−8884.
DOI: dx.doi.org/10.1021/acs.chemmater.2c02177

 

328

J. Shao, R. Breuer, M. Schmittel, T. Ye,
Potential-dependent Adhesion Forces Between dsDNA and Electroactive Surfaces,
Langmuir, 2022, 38, 11899–11908.
DOI: dx.doi.org/10.1021/acs.langmuir.2c01515

 

327

S. Kundu, D. Mondal, E. Elramadi, I. Valiyev, M. Schmittel,
Parallel Allosteric Inhibition of Shuttling Motion and Catalysis in a Silver(I)-loaded [2]Rotaxane,
Org. Lett. 2022, 24, 6609-6613.
DOI: dx.doi.org/10.1021/acs.orglett.2c02609

 

326

S. Kundu, A. Ghosh, I. Paul, M. Schmittel,
Multicomponent Pseudorotaxane Quadrilateral as Dual-Way Logic AND Gate with Two Catalytic Outputs,
J. Am. Chem. Soc. 2022, 29, 13039-13043.
DOI: dx.doi.org/10.1021/jacs.2c05065

 

325

E. Elramadi, A. Ghosh, I. Valiyev, P. K. Biswas, T. Paululat, M. Schmittel,
Catalytic machinery in motion: Controlling catalysis via speed,
Chem. Commun. 2022, 58, 8073-8076.
DOI: dx.doi.org/10.1039/D2CC02555H

 

324P. Howlader, M. Schmittel,
Heteroleptic metallosupramolecular aggregates/complexation for supramolecular catalysis,
Beilstein J. Org. Chem. 2022, 18, 597-630.
DOI: dx.doi.org/10.3762/bjoc.18.62

 

  
323

I. Valiyev, A. Ghosh, I. Paul, M. Schmittel,
Concurrent Base and Silver(I) Catalysis Pulsed by Fuel Acid,
Chem. Commun. 2022, 58, 1728–1731.   
DOI: dx.doi.org/10.1039/d1cc06398g

322

M. Schmittel,
Switchable Catalysis Using Allosteric Effects,
in Supramolecular Catalysis: New Directions and Developments, Eds. Matthieu Raynal and Piet van Leeuwen, Wiley 2022, Chapter 39, p. 575-589.
Print ISBN:9783527349029
DOI: dx.doi.org/10.1002/9783527832033.ch39

 

 321

L. Grossmann, D. A. Duncan, S. P. Jarvis, R. G. Jones, S. De, J. Rosen, M. Schmittel, W. M. Heckl, Jonas Björk, M. Lackinger,
Evolution of Adsorption Heights in the On-Surface Synthesis and Decoupling of Covalent Organic Networks on Ag(111) by Normal-Incidence X-ray Standing Wave,
Nanoscale Horizons, 2022, 7, 51-62.
DOI: dx.doi.org/10.1039/D1NH00486G

 

321

 

 320

 

 

D. Mondal, A. Ghosh, I. Paul, M. Schmittel,
Fuel Acid Drives Base Catalysis and Supramolecular Cage-to-Device Transformation Under Dissipative Conditions,
Org. Lett. 2022, 24, 69–73.
DOI: dx.doi.org/10.1021/acs.orglett.1c03654

320

       2021      ↑

 

319

A. Ghosh, I. Paul, M. Schmittel,
Cooperative Effects in Switchable Catalysis: Enhancing Double-Click Reaction Yield of Symmetrical Rotaxanes,
Angew. Chem. Int. Ed. 2021, 60, 20558– 20562.
DOI:10.1002/anie.202108269
Kooperative Effekte in schaltbarer Katalyse: Verbesserung der Doppel-Click-Reaktionsausbeuten von symmetrischen Rotaxanen,
Angew. Chem. 2021, 133, 20722–20727.
DOI:10.1002/ange.202108269

319

318

A. Goswami, S. Saha, E. Elramadi, A. Ghosh, M. Schmittel,
Off-Equilibrium Speed Control of a Multistage Molecular Rotor: 2‑Fold Chemical Fueling by Acid or Silver(I),
J. Am. Chem. Soc. 2021, 143, 14926–14935.
DOI:10.1021/jacs.1c08005

 

317

A. Goswami, M. S. Özer, I. Paul, M. Schmittel,
Evolution of catalytic machinery: Three-component nanorotor catalyzes formation of four-component catalytic machinery,
Chem. Commun. 2021, 57, 7180-7183.
DOI:10.1039/d1cc02805g

316

A. Ghosh, I. Paul, M. Schmittel,
Multitasking with Chemical Fuel: Dissipative Formation of a Pseudorotaxane Rotor from Five Distinct Components,
J. Am. Chem. Soc. 2021, 143, 5319–5323.
DOI:10.1021/jacs.1c01948

 316

315 A. Goswami, S. Gaikwad, M. Schmittel,
A Switchable Catalyst Duo for Acyl Transfer Proximity Catalysis and Regulation of Substrate Selectivity,
Chem. Eur. J. 2021, 27, 2997-3001.
DOI:10.1002/chem.202004416
313
314

Y. Li, A. Ghosh, P. K. Biswas, S. Saha, M. Schmittel,
Exchange Speed of Four-component Nanorotors Correlates with Hammett Substituent Constants,
Chemistry, 2021, 3, 116–125.
DOI:10.3390/chemistry3010009

 314-b

313M. Schmittel, P. Howlader,
Toward Molecular Cybernetics - the Art of Communicating Chemical Systems,
Chem. Rec. 2021, 21, 523-543.
   

2020     ↑

 312

 

 

A. Ghosh, M. Schmittel,
Using multiple self-​sorting for switching functions in discrete multicomponent systems,
Beilstein J. Org. Chem. 2020, 16, 2831–2853.
DOI:10.3762/bjoc.16.233

310

 311P. K. Biswas, A. Goswami, S. Saha, M. Schmittel,
Dynamics of Hydrogen Bonding in Three-​Component Nanorotors,
Chem. Eur. J. 2020, 26, 14095-14099.
DOI:10.1002/chem.202002877
311
310V. V. Rajasekaran, I. Paul, M. Schmittel,
Reversible switching from a three- to a nine-​fold degenerate dynamic slider-​on-​deck through catenation,
Chem. Commun. 2020, 56, 12821-12824.
DOI:10.1039/D0CC05578F
312

 309

 

 

 

M. Schmittel, A. Goswami, I. Paul, P. K. Biswas,
Motion and Nanomechanical Effects in Supramolecular Catalysts,
C. Joachim (ed.), Building and Probing Small for Mechanics, Advances in Atom and Single Molecule Machines,
© Springer International Publishing, Springer Nature Switzerland AG, 2020, Pages 195-218, ISBN 978-3-030-56777-4
DOI: /10.1007/978-3-030-56777-4

 308

A. Goswami, M. Schmittel,
Double Rotors with Fluxional Axles: Domino Rotation and Azide-Alkyne Huisgen Cycloaddition Catalysis,
Angew. Chem. Int. Ed. 2020, 59, 12362–12366.
DOI: /10.1002/anie.202002739
Doppelrotoren mit fluktuierenden Achsen: Domino-Rotation und Katalyse der Azid-Alkin-Huisgen-Cycloaddition
Angew. Chem. 2020, 132, 12461 –12465.
DOI: /10.1002/ange.202002739

 

 

 

 307

S. Saha, A. Ghosh, T. Paululat, M. Schmittel,
Allosteric Regulation of Rotational, Optical and Catalytic Properties within Multicomponent Machinery,
Dalton Trans. 2020, 49, 8693–8700.
DOI: /10.1039/d0dt01961e

 306

P. K. Biswas, S. Saha, S. Gaikwad, M. Schmittel,
Reversible Multicomponent AND Gate Triggered by Stoichiometric Chemical Pulses Commands the Self-Assembly and Actuation of Catalytic Machinery,
J. Am. Chem. Soc. 2020, 142, 7889–7897.
DOI: /10.1021/jacs.0c01315

 305

A. Goswami, S. Saha, P. Biswas, M. Schmittel,
(Nano)mechanical Motion Triggered by Metal Coordination: from Functional Devices to Networked Multicomponent Catalytic Machinery,
Chem. Rev. 2020, 120, 125-199.
DOI: /10.1021/acs.chemrev.9b00159

305
 304

N. Mittal, I. Paul, S. Pramanik, M. Schmittel,
Remote control of the reversible assembly/disassembly of supramolecular aggregates,
Supramol. Chem. 2020, 32, 133-138.
DOI: /10.1080/10610278.2020.1711907

304

2019     ↑

 303

S. Saha, P. K. Biswas, I. Paul,
Selective and Reversible Interconversion of Nanosliders Commanded by Remote Control via Metal-Ion Signaling,
Chem. Commun. 2019, 55, 14733- 14736.
DOI: /10.1039/c9cc07415e

303
 302

 A. Ghosh, I. Paul, M. Schmittel,
Time-Dependent Pulses of Lithium Ions in Cascaded Signaling and Out-of-Equilibrium (Supra)Molecular Logic,
J. Am. Chem. Soc. 2019, 141, 18954-18957.
DOI: /10.1021/jacs.9b10763

302
 301

 I. Paul, A. Ghosh, M. Bolte, M. Schmittel,
Remote Control of the Synthesis of a [2]Rotaxane and its Shuttling via Metal-ion Translocation, (special issue: 80th birthday of J.-M. Lehn)
ChemistryOpen 2019, 8, 1355–1360.
DOI: /10.1002/open.201900293

301
 300

 A. Goswami, T. Paululat, M. Schmittel,
Switching Dual Catalysis without Molecular Switch: Using A Multi-Component Information System for Reversible Reconfiguration of Catalytic Machinery,
J. Am. Chem. Soc. 2019, 141, 15656-15663.
DOI: /10.1021/jacs.9b07737

300
 299

S. Gaikwad,  M. S. Özer, S. Pramanik, M. Schmittel,
Three-State Switching in a Double-Pole Change-Over Nanoswitch Controlled by Redox-Dependent Self-Sorting,
Org. Biomol. Chem. 2019, 17, 7956–7963.
DOI: /10.1039/c9ob01456j

299
 298

M. S. Özer, I. Paul, A. Goswami, M. Schmittel,
Cation exchange reversibly switches rotor speed and is monitored by a networked fluorescent reporter,
Dalton Trans. 2019, 48, 9043–9047.
DOI: /10.1039/c9dt01633c

298
 297

I. Paul, D. Samanta, S. Gaikwad, M. Schmittel,
Selective detection of DABCO using a supramole¬cular interconversion as fluorescence reporter,
Beilstein J. Org. Chem. 2019, 15, 1371–1378.
DOI: /10.3762/bjoc.15.137

297
 296

M. Schmittel,
Dynamic Functional Molecular Systems: From Supramolecular Structures to Multi-component Machinery and to Molecular Cybernetics,
Israel J. Chem. 2019, 59, 197–208.
DOI: /10.1002/ijch.201800124

296
 295

I. Paul, N. Mittal, S. De, M. Bolte, M. Schmittel,
Catch-Release System for Dosing and Recycling Silver(I) Catalyst with Status of Catalytic Activity Reported by Fluorescence,
J. Am. Chem. Soc. 2019, 141, 5139–5143.
DOI: /10.1021/jacs.9b01182

295
 294

S. Saha, P. K. Biswas, M. Schmittel,
Reversible Interconversion of a Static Metallosupramolecular Cage Assembly into a High-Speed Rotor – Stepless Adjustment of Rotational Exchange by Nucleophile Addition,
Inorg. Chem. 2019, 58, 3466–3472.
DOI: /10.1021/acs.inorgchem.8b03567

294

2018     ↑

   
 293

A. Ghosh, I. Paul, S. Saha, T. Paululat,  M. Schmittel,
Machine Metathesis: Thermal and Catalyzed Exchange of Piston Rods in Multicomponent Nanorotor/Nanoslider Ensemble,
Org. Lett. 2018, 20, 7973–7976.
DOI: /10.1021/acs.orglett.8b03541

293
 292 M. S. Özer, N. Mittal, S. Gaikwad, M. Schmittel,
Multi-Component Spirane Assemblies,
Macromol. Chem. Phys. 2018, 219, 1800218
DOI: /10.1002/macp.201800218

 291

M. Fritton, K. Otte, J. Björk, P. K. Biswas, W. M. Heckl, M. Schmittel, M. Lackinger,
The influence of ortho-methyl substitution in organometallic self-assembly – a comparative study on Cu(111) vs. Ag(111),
Chem. Commun. 2018, 70, 9745-9748.
DOI: /10.1039/c8cc04854a

291
 290

A. Goswami, M. Schmittel,
Heteroleptic copper phenanthroline complexes in motion: From stand-alone devices to multi-component machinery,
Coord. Chem. Rev. 2018, 376, 478-505.
DOI: /10.1016/j.ccr.2018.08.011

290
 289

G. F. Bucher, M. Lal, A. Rana, M. Schmittel,
Fragmentation of a Dioxolanyl Radical via Nonstatistical Reaction Dynamics: Characterization of the Vinyloxy Radical by ns Time-Resolved Laser Flash Photolysis,
Phys. Chem. Chem. Phys. 2018, 20, 19819-19828.
DOI: /10.1039/c8cp03311k

 289
 288

M. Lischka, G. S. Michelitsch, N. Martsinovich, J. Eichhorn, A. Rastgoo-Lahrood, T. Strunskus, R. Breuer, K. Reuter, M. Schmittel, W. M. Heckl, Markus Lackinger,
Remote functionalization in surface-assisted Ullmann reaction guided by conformational mechanics: organometallic self-assembly of 3,3',5,5'-tetrabromo-2,2',4,4',6,6'-hexafluorobiphenyl on Ag(111),
Nanoscale 2018, 10, 12035-12044.
DOI: /10.1039/c8nr01987h

288
 287

U. Lüning, M. Schmittel,
Christoph Rüchardt (1929-2018) – Experte der Physikalisch-Organischen Chemie
Angew. Chem. 2018, 130, 6847.
DOI: /10.1002/ange.201803690
Christoph Rüchardt (1929-2018) – Expert in Physical-Organic Chemistry
Angew. Chem. Int. Ed. 2018, 57, 6735.
DOI: /10.1002/anie.201803690

287
 286

M. E. Cinar, M. Lal, J. Schlirf, H.-J. Deiseroth, M. Schmittel,
Detection and Follow-up Reactions of Distonic ?,?-Dimesityl Enol Radical Cations Containing Nitrogen Heterocyclic Bases,
J. Phys. Org. Chem. 2018, e3865.
DOI: /10.1002/poc.3865

 
 285

P. Biswas, S. Saha, T. Paululat, M. Schmittel,
Rotating Catalysts Are Superior – Suppressing Product Inhibition by Anchimeric Assistance in Four-Component Catalytic Machinery,
J. Am. Chem. Soc. 2018, 140, 9038–9041.
DOI: /10.1021/jacs.8b04437
Cover Picture: https://pubs.acs.org/subscribe/covers/jacsat/jacsat_v140i029-4.jpg?radn=613882810633525?0.48609523822478684

285 
 284

M. Schmittel,
Networking switches for smart functions using copper signaling and dynamic heteroleptic complexation,
Dalton Trans. 2018, 47, 6654–6659.
DOI: /10.1039/C8DT01010B

284
 283

A. Goswami, S. Pramanik, M. Schmittel,
Catalytically Active Nanorotor Reversibly Self-Assembled by Chemical Signaling within an Eight-Component Network,
Chem. Commun. 2018, 57, 54, 3955 – 3958.
DOI: /10.1039/C8CC01496E

Highlighted in Chemistry World: https://www.chemistryworld.com/news/catalytic-nanomachine-assembled-by-remote-control/3008981.article
 

282
 282

N. Mittal, M. S. Özer, M. Schmittel,
Four-Component Catalytic Machinery: Reversible Three-State Control of Organocatalysis by Walking Back and Forth on Track,
Inorg. Chem. 2018, 57, 3579–3586.
DOI: /10.1021/acs.inorgchem.7b02703

281
 281

M. Schmittel, S. Saha,
From self-sorting of dynamic metal-ligand motifs to (supra)molecular machinery in action,
Adv. Inorg. Chem. 2018, 71, 135–176.
DOI: /10.1016/bs.adioch.2017.11.006
 280

A. Ghosh, I. Paul, M. Adlung, C. Wickleder, M. Schmittel,
Oscillating Emission of [2]Rotaxane Driven by Chemical Fuel, 
Org. Lett. 2018, 20, 1046–1049.
DOI: /10.1021/acs.orglett.7b03996

279
 279

M. V. Sheridan, P. Gamm, S. T. Schneebeli, R. Breuer, M. Schmittel, W.E. Geiger,
The Effect of Large Electrolyte Anions on the Sequential Oxidations of Bis(fulvalene)diiron Attached to Glassy Carbon by an Ethynyl Linkage,
Langmuir 2018, 34, 1327–1339.
DOI: /10.1021/acs.langmuir.7b03649

278
 278

S. Gaikwad, S. Pramanik, S. De, M. Schmittel,
High-speed network of nanoswitches for on/off control of catalysis,
Dalton Trans. 2018, 47, 1786–1790.
DOI: /10.1039/c7dt04695b

277
 277

I. Paul, A. Goswami, N. Mittal, M. Schmittel,
Catalytic Three-Component-Machinery: Control of Catalytic Activity by Machine Speed,
Angew. Chem. Int. Ed. 2018, 57, 354 –358.
DOI: /10.1002/anie.201709644

Katalytische Drei-Komponenten-Maschinen: Steuerung der katalytischen Aktivität mittels Maschinengeschwindigkeit,
Angew. Chem. 2018, 130, 360 –364.
DOI: /10.1002/ange.201709644

276

2017     ↑

 276

A. Rana, I. Paul, M. Schmittel,
Dynamic Effects in the Didehydro–Diels–Alder (DDDA) Reaction of Enyne–Ketoenes: 50% Stepwise Bond Formation in Spite of Concerted Transition State,
J. Phys. Org. Chem. 2017, e3732.
DOI: /10.1002/poc.3732
 275

D. Samanta, I. Paul, M. Schmittel,
Supramolecular five-component nano-oscillator,
Chem. Commun. 2017, 53, 9709-9712.
DOI: /10.1039/C7CC05235

275
 274

M. S. Özer, A. Rana, P. Biswas, M. Schmittel,
Four-component zinc-porphyrin / zinc-salphen nanorotor,
Dalton Trans. 2017, 46, 9491–9497.
DOI: /10.1039/c7dt01323j

274
 273

S. Gaikwad, M. L. Saha, D. Samanta, M. Schmittel,
Five-component trigonal nanoprism with six dynamic corners,
Chem. Commun. 2017, 53, 8034–8037.
DOI: /10.1039/c7cc04078d

273
 272

P. K. Biswas, S. Saha, Y. Nanaji, A. Rana, M. Schmittel,
Influence of Rotator Design on the Speed of Self-assembled Four-component Nanorotors: Coordinative vs. Dispersive Interactions,
Inorg. Chem. 2017, 56, 6662–6670.
DOI: /10.1021/acs.inorgchem.7b00740

272
 271

A. Goswami, I. Paul, M. Schmittel,
Three-Component Nanorotors Generated from Fusion of Complexes and Post-Fusion Metal-Metal Exchange,
Chem. Commun. 2017, 53, 5186 - 5189.
DOI: /10.1039/c7cc01977g
 270

N. Mittal, S. Pramanik, I. Paul, S. De, M. Schmittel,
Networking Nanoswitches for ON/OFF Control of Catalysis,
J. Am. Chem. Soc. 2017, 139, 4270–4273.
DOI: /10.1002/anie.201608184

270
 269

A. Rastgoo-Lahrood, M. Lischka, J. Eichkorn, D. Samanta, M. Schmittel, W. M. Heckl, M. Lackinger,
Reversible intercalation of iodine monolayers between on-surface synthesized covalent polyphenylene networks and Au(111),
Nanoscale, 2017, 9, 4995-5001.
DOI: /10.1002/anie.201608184

269
 268

M. Schmittel,
Author profile (Michael Schmittel),
Angew. Chem. Int. Ed. 2017, 56, 2538.
DOI: /10.1002/anie.201608184
Angew. Chem. 2017, 129, 2580.
DOI: /10.1002/ange.201608184
 267

S. Gaikwad, M. Schmittel,
Five-State Rotary Nanoswitch,
J. Org. Chem. 2017, 82, 343–352.
DOI: /10.1021/acs.joc.6b02436

2016     ↑

 266

A. Rastgoo-Lahrood, N. Martsinovich, M. Lischka, J. Eichhorn, P. Szabelski, D. Nieckarz, T. Strunskus, K. Das, M. Schmittel, W. M. Heckl, M. Lackinger,
From Au-thiolate chains to thioether Sierpinski triangles: the versatile surface chemistry of 1,3,5-tris(4-mercaptophenyl)benzene on Au(111)
ACS Nano 2016, 10, 10901–10911.
DOI: /10.1021/acsnano.6b05470
 265
M. L. Saha, M. Schmittel,
Metal-Ligand Exchange in a Cyclic Array – The Stepwise Advancement of Supramolecular Complexity,
Inorg. Chem. 2016, 55, 12366–12375.
DOI: /10.1021/acs.inorgchem.6b02256
 264
M. E. Cinar, M. Schmittel,
Highly stereoselective metal-mediated domino aldol reactions of propiophenone enolates with heteroaromatic, aliphatic and unsaturated aldehydes,
Monatsh. Chem. 2016, 147, 1925−1932.
DOI: /10.1007/s00706-016-1841-4
264
 263

D. Song, K. Chen, M. Schmittel, H. Schönherr,
AFM Study of Surface Nanobubbles on Binary Self-Assembled Monolayers on Ultraflat Gold with Identical Macroscopic Static Water Contact Angles and Different Terminal Functional Groups,
Langmuir 2016, 32, 11172−11178.
DOI:/10.1021/acs.langmuir.6b01775
 262

K. Chen, M. Schmittel,
An iridium(III) complex as a versatile platform for molecular logic gates: an integrated full subtractor and 1:2 demultiplexer,
Anal. Bioanal. Chem. 2016, 408, 7077–7083.
DOI:/10.1007/s00216-016-9443-x
 261

S. Gaikwad, A. Goswami, S. De, M. Schmittel,
Metallregulierter vierstufiger Nanoschalter steuert zweistufige sequentielle Katalyse in einem 11-Komponentensystem,
Angew. Chem. 2016, 128, 10668–10673. DOI:/10.1002/ange.201604658
A Metalloregulated Four-State Nanoswitch Controls Two-Step Sequential Catalysis in an Eleven-Component System,
Angew. Chem. Int. Ed. 2016, 55, 10512 –10517. DOI:/10.1002/anie.201604658

261
 260

A. Rastgoo-Lahrood, J. Björk, M. Lischka, J. Eichkorn, S. Kloft, M. Fritton, T. Strunskus, D. Samanta, M. Schmittel, W. M. Heckl, M. Lackinger,
Post-Synthetic Decoupling of On-Surface Synthesized Covalent Nano¬struc¬tures from Ag(111),
Angew. Chem. Int. Ed. 2016, 55, 7650–7654. DOI:/10.1002/anie.201600684
Postsynthetische Entkopplung oberflächensynthetisierter kovalenter Nano¬strukturen von Ag(111),
Angew. Chem. 2016, 128, 7780–7784. DOI:/10.1002/ange.201600684

260
259

N. Mittal, M. L. Saha, M. Schmittel,
Fully reversible three-state interconversion of metallosupramolecular architectures,
Chem. Commun. 2016, 52, 8749–8752. DOI:/10.1039/c6cc03824g

259
258

M. E. Cinar, B. Engelen, M. Panthöfer, H.-J. Deiseroth, J. Schlirf, M. Schmittel,
Scope and Mechanism of the Highly Stereoselective Metal-Mediated Domino Aldol Reactions of Enolates with Aldehydes,
Beilstein J. Org. Chem. 2016, 12, 813–824. DOI:/10.3762/bjoc.12.80

258
257

S. K. Samanta, A. Rana, M. Schmittel,
Konformativer Schlupf bestimmt die Rotationsfrequenz in 5-Komponenten-Nanorotoren,
Angew. Chem. 2016, 128, 2309-2314. DOI:/10.1002/ange.201509108
Conformational Slippage Determines Rotational Frequency in Five-Component Nanorotors,
Angew. Chem. Int. Ed. 2016, 55, 2267-72. DOI:/10.1002/anie.201509108

257
256

A. Rana, E. M. Cinar, D. Samanta, M. Schmittel,
Mechanistic Information From Nonstationary Points,
Org. Lett. 2016, 18, 84–87. DOI:/10.1021/acs.orglett.5b03310

 256
255

Anup Rana, Mehmet Emin Cinar, Debabrata Samanta, and Michael Schmittel
Solving the Puzzling Competition of the Thermal C2–C6 vs. Myers–Saito Cyclization of Enyne–Carbodiimides,
Beilstein J. Org. Chem. 2016, 12, 43-49. DOI:/10.3762/bjoc.12.6

255

 2015     ↑
 254

N. Mittal, M. L. Saha, M. Schmittel,
Seven–component metallosupramolecular quadrilateral with four different orthogonal complexation vertices,
Chem. Commun. 2015, 51, 15514-15517. DOI:/10.1039/c5cc06324h

254

 253

M. Schmittel,
From self-sorted coordination libraries to networking nanoswitches for catalysis,
Chem. Commun. 2015, 51, 14956—14968. DOI:/10.1039/C5CC06605K

253

 252

M. E. Cinar, M. Schmittel,
A One-Pot Domino Aldol Reaction of Indium Enolates Affording 6-Deoxy-α-D,L-altropyranose Derivatives: Synthesis, Mechanism and Computational Results,
J. Org. Chem. 2015, 80, 8175-8182. DOI:/10.1021/acs.joc.5b01256
 251

M. Schmittel,* S. De, S. Pramanik,
Redox‐dependent self‐sorting toggles a rotary nanoswitch,
Org. Biomol. Chem. 2015, 15, 8937-8944. DOI:/10.1039/c5ob01041a

251

 250

L. Yuan, R. Breuer, L. Jiang, M. Schmittel, C. Nijhuis,
A Molecular Diode with a Statistically Robust Rectification Ratio of Three Orders of Magnitude,
Nano Lett. 2015, 15, 5506–5512. DOI:/10.1021/acs.nanolett.5b02014
 249

D. Samanta, A. Rana, M. Schmittel,
Nonstatistical Dynamics in the Thermal C2-C6/Diels-Alder Cyclization of Enyne-Allenes: Effect of Topology,
J. Org. Chem. 2015, 80, 2174–2181. DOI:/10.1021/jo502693b

249
 248

K. Chen, Q. Shu, M. Schmittel,
Design Strategies for Lab-on-a-Molecule Probes and Orthogonal Sensing,
Chem. Soc. Rev. 2015, 44, 136–160. DOI:/10.1039/c4cs00263f

248

2014     ↑    
 247

D. Samanta, A. Rana, J. W. Bats, M. Schmittel,
A One-Pot Multistep Cyclization Yielding Thiadiazoloimidazol Derivatives,
Beilstein J. Org. Chem. 2014, 10, 2989–2996. DOI:/10.3762/bjoc.10.317

247

 246

M. E. Cinar, G. Morbach, M. Schmittel,
Thermal Reactivity of Neutral and Oxidized Ferrocenyl-Substituted Enediynes,
Molecules 2014, 19, 18399-18413. DOI:/10.3390/molecules191118399
Invited article: John C. Walton and Francon Williams
 245

S. De, S. Pramanik, M. Schmittel,
A Toggle Nanoswitch Alternately Controlling Two Catalytic Reactions,
Angew. Chem. Int. Ed. 2014, 53, 14255-14259. DOI:/10.1002/anie.201408457
Ein Nanowechselschalter zur Kontrolle zweier katalytischer Prozesse,
Angew. Chem. 2014, 5126, 14480 –14484. DOI:/10.1002/ange.201408457

245

 244

S. Pramanik, S. De, M. Schmittel,
A Trio of Nanoswitches in Redox-Potential Controlled Communication,
Chem. Commun. 2014, 50, 13254–13257. DOI:/10.1039/c4cc05773b

244

 243

D. Samanta, A. Rana, M. Schmittel,
Nonstatistical Dynamics in the Thermal Garratt-Braverman/[1,5]-H Shift of Ene-diallene: An Experimental and Computational Study,
J. Org. Chem. 2014, 79, 8435-8439, DOI:/10.1021/jo501324w

243

 242

M. L. Saha, N. Mittal, J. W. Bats, M. Schmittel,
A six–component metallosupramolecular pentagon via self-sorting,
Chem. Commun. 2014, 50, 12189–12192. DOI:/10.1039/C4CC05465B

242

 241

J. Eichhorn, D. Nieckarz, O. Ochs, D. Samanta, M. Schmittel, P. J. Szabelski, M. Lackinger,
On-Surface Ullmann Coupling: The Influence of Kinetic Reaction Parameters on the Morphology and Quality of Covalent Networks,
ACS Nano 2014, 8, 7880–7889. DOI:/10.1021/nn501567p

241

 240

M. E. Cinar, C. Vavilala, R. Jaquet, J. W. Bats, M. Schmittel,
Fluoro-Ene Reaction vs. [2+2] Cycloaddition in the Thermal C2-C6 Cyclization of Enyne-Allenes: An Experimental and Theoretical Investigation,
Eur. J. Org. Chem. 2014, 5166–5177. DOI:/10.1002/ejoc.201402438

240

 239

S. De, S. Pramanik, M. Schmittel,
Monomer-dimer nanoswitch that mimics the working principle of the SARS-CoV 3CLpro enzyme controls copper-catalysed cyclopropanation,
Dalton Trans. 2014, 43, 10977 – 10982. DOI:/10.1039/c4dt01508h

239

 238

J. Eichhorn, T. Strunskus, A. Rastgoo-Lahrood, D. Samanta, M. Schmittel, M. Lackinger,
On-Surface Ullmann Polymerization via Intermediate Organometallic Networks on Ag(111),
Chem. Commun. 2014, 50, 7680 – 7682. DOI:/10.1039/C4CC02757D

238

 237

S. K. Samanta, A. Rana, M. Schmittel,
Reversible cargo shipping between orthogonal stations of a nanoscaffold upon redox input,
Dalton Trans. 2014, 43, 9438–9447. DOI:/10.1039/C4DT00849A

237

 236

K. Chen, M. Schmittel,
Triple-channel lab-on-a-molecule for triple-anion quantification using an iridium(III)-imidazolium conjugate,
Chem. Commun. 2014, 50, 5756 – 5759. DOI:/10.1039/C4CC01421A
Hot paper in May:
http://blogs.rsc.org/cc/2014/05/06/hot-chemcomm-articles-for-may-2/
 235

S. Pramanik, S. De, M. Schmittel,
Bidirectional Chemical Communication between Nanomechanical Switches,
Angew. Chem. Int. Ed. 2014, 53, 4709-4713. DOI:/10.1002/anie.201400804
Bidirektionale Chemische Kommunikation zwischen nanomechanischen Schaltern,
Angew. Chem. 2014, 126, 4798-4803. DOI:/10.1002/ange.201400804

235
 234

D. Samanta, A. Rana, M. Schmittel,
Quantification of non-statistical dynamics in an intramolecular Diels-Alder cyclisation without trajectory computation,
J. Org. Chem. 2014, 79, 2368-2376. DOI:/10.1021/jo500035b
http://pubs.acs.org/articlesonrequest/AOR-yNpFpCs8dyHQiCzH4HSQ

234
 233

M. L. Saha, S. Neogi, M. Schmittel,
Dynamic heteroleptic metal-phenanthroline complexes: from structure to function,
Dalton Trans. 2014, 43, 3815 – 3834. DOI:/10.1039/C3DT53570C

233
 232

S. K. Samanta, J. W. Bats, M. Schmittel,
A five-component nanorotor with speed regulation,
Chem. Commun. 2014, 50, 2364 – 2366. DOI:/10.1039/C3CC49476D

232

 2013     ↑
231

S. K. Samanta, M. Schmittel,
Four-Component Supramolecular Nanorotors,
J. Am. Chem. Soc. 2013, 135, 18794–18797. DOI:/10.1021/ja411011a

231
230

M. L. Saha, M. Schmittel,
From 3-Fold Completive Self-Sorting of a Nine-Component Library to a Seven-Component Scalene Quadrilateral
J. Am. Chem. Soc. 2013, 135, 17743–17746. DOI:/10.1021/ja410425k

230

229

K. Chen, J. W. Bats, M. Schmittel,
Iridium-Based Lab-on-a-Molecule for Hg2+ and ClO– with Two Distinct Light-Up Emissions,
Inorg. Chem. 2013, 52, 12863–12865. DOI:/10.1021/ic401983h

229
228

K. Chen, C. Adam, N. Sojic, M. Schmittel,
Photochemical functionalisation of optical nanotips with a rhodamine chemosensor for remote through-fiber detection of Hg2+,
RSC Adv. 2013, 3, 24140 – 24145. DOI:/10.1039/c3ra45198d

228
227

P. Natarajan, M. Schmittel,
Photoluminescence, Redox Properties and Electrogenerated Chemiluminescence of Twisted 9,9' Bianthryls,
J. Org. Chem. 2013, 78, 10383-10394. DOI:/10.1021/jo401785c

227
226

R. Breuer, M. Schmittel,
Unsymmetrically Substituted 1,1' -Biferrocenylenes Maintain Class III Mixed-Valence Character,
Organometallics 2013, 32, 5980–5987. DOI:/10.1021/om400502e

226
225

S. De, S. Pramanik, M. Schmittel,
Dual coordination in ditopic azabipyridines and azaterpyridines as a key for reversible switching,
Dalton Trans. 2013, 42, 15391–15398. DOI:/10.1039/c3dt51780b

225
224

K. Chen, M. Schmittel,
Iridium(III)-based lab-on-a-molecule for cysteine/homocysteine and tryptophan using triple-channel interrogation
Analyst 2013, 138, 6742–6745. DOI:/10.1039/c3an01530k

224
223

S. Khatua, M. Schmittel,
A Single Molecular Light-up Sensor for Quantification of Hg2+ and Ag+ in Aqueous Medium: High Selectivity towards Hg2+ over Ag+ in a Mixture,
Org. Lett. 2013, 12, 4422-4425. DOI:/10.1021/ol401970n

223
222

T. Sirtl, W. Song, G. Eder, S. Neogi, M. Schmittel, W. M. Heckl, M. Lackinger,
Solvent-Dependent Stabilization of Metastable Monolayer Polymorphs at the Liquid-Solid Interface,
ACS Nano 2013, 7, 6711–6718. DOI:/10.1021/nn4014577

222
221

M. L. Saha, K. Mahata, D. Samanta, V. Kalsani, J. Fan, J. W. Bats, M. Schmittel,
A phenanthroline-terpyridine hybrid as a chameleon-type ligand in a reversible metallosupramolecular rearrangement,
Dalton Trans. 2013, 42, 12840 – 12843. DOI:/10.1039/C3DT51351C

221
220

M. Lal Saha, J. W. Bats, M. Schmittel,
Merging strong and weak coordination motifs in the integrative self-sorting of a 5-component trapezoid and scalene triangle,
Org. Biomol. Chem. 2013, 11, 5592–5595. DOI:/10.1039/c3ob41258j
Highlighted as inside cover page and as hot article: http://pubs.rsc.org/en/content/articlepdf/2013/ob/c3ob90115g?page=search

220
219

P. Natarajan, M. Schmittel,
ON-OFF Luminescence Signaling of Organic-Inorganic Hybrids Switches,
Inorg. Chem. 2013, 52, 8579–8590. DOI:/10.1021/ic400676j
Highlighted as TOC graphic on the module located on the IC homepage!

219
218

M. L. Saha, S. De, S. Pramanik, M. Schmittel,
Orthogonality in Discrete Self-Assembly – survey of current concepts,
Chem. Soc. Rev. 2013, 42, 6860–6909. DOI:/10.1039/C3CS60098J

218
217

Q. Shu, C. Adam, N. Sojic, M. Schmittel,
Electrochemiluminescent polymer film with suitable redox “turn-off” absorbance window for remote selective sensing of Hg2+,
Analyst 2013, 138, 4500-4504. DOI:/10.1039/C3AN00545C

217
216

S. Neogi, Y. Lorenz, M. Engeser, D. Samanta, M. Schmittel,
Heteroleptic Metallosupramolecular Racks, Rectangles and Trigonal Prisms – Stoichiometry-Controlled Reversible Interconversion,
Inorg. Chem. 2013, 52, 6975–6984. DOI:/10.1021/ic400328d

216
215

T. Sirtl, J. Jelic, J. Meyer, K. Das, W. M. Heckl, W. Moritz, J. Rundgren, M. Schmittel, K. Reuter, M. Lackinger,
Adsorption structure determination of a large polyaromatic trithiolate on Cu(111): combination of LEED-I(V) and DFT-vdW,
Phys. Chem. Chem. Phys. 2013, 15, 11054-11060. DOI:/10.1039/C3CP50752A

215
214

S. K. Samanta, M. Schmittel,
Guest Encapsulation and Coronene-C60 Exchange in Supramolecular Zinc Porphyrin Tweezers, Grids and Prisms,
Org. Biomol. Chem. 2013, 11, 3108 - 3115. DOI:/10.1039/C3OB27481K

214
213

K. Chen, Michael Schmittel,
Reversible binding and quantification of heparin and chondroitin sulfate in water using redoxstable biferrocenylene SAMs,
Analyst 2013, 138, 2405 – 2410. DOI:/10.1039/C3AN36781A

213
212

D. Samanta, M. E. Cinar, K. Das, M. Schmittel,
Non-Statistical Dynamic Effects in the Thermal C2-C6 Diels-Alder Cyclization of Enyne-Allenes,
J. Org. Chem. 2013, 78, 1451–1462. DOI:/10.1021/jo302524a

212
211

T. Sirtl, S. Schlögl, A. Rastgoo-Lahrood, J. Jelic, S. Neogi, M. Schmittel, W. M. Heckl, K. Reuter, M. Lackinger,
Control of Intermolecular Bonds by Deposition Rates at Room Temperature: Hydrogen Bonds vs. Metal Coordination in Trinitrile Monolayers,
J. Am. Chem. Soc. 2013, 135, 691–695. DOI:/10.1021/ja306834a

211

 2012     ↑
210

Q. Shu, L. Birlenbach, M. Schmittel,
A Bisferrocenylphenanthroline Iridium(III) Complex as a Lab-on-a-Molecule for Cyanide and Fluoride in Aqueous Solution,
Inorg. Chem. 2012, 51, 13123–13127. DOI:/10.1021/ic301256g

210
209

M. Schmittel, S. Pramanik, S. De,
A Reversible Nanoswitch as ON/OFF Photocatalyst,
Chem. Commun. 2012, 48, 11730-11732. DOI:/10.1039/C2CC36408E

209
208

S. Neogi, G. Schnakenburg, Y. Lorenz, M. Engeser, M. Schmittel,
Implications of Stoichiometry-Controlled Structural Changeover Between Heteroleptic Trigonal [Cu(phenAr2)(py)]+ and Tetragonal [Cu(phenAr2)(py)2]+ Motifs for Solution and Solid-State Supramolecular Self-Assembly,
Inorg. Chem. 2012, 51, 10832–10841. DOI:/10.1021/ic301286w

208
207

P. Natarajan, M. Schmittel,
9,10-Diarylanthracenes as Stable Electrochemiluminescent Emitters in Water,
J. Org. Chem. 2012, 77, 8669–8677. DOI:/10.1021/jo301616t

207
206

R. Breuer, M. Schmittel,
Redox Stable SAMs in Water (pH 0 – 12) from 1,1'-Biferrocenylene-Terminated Thiols on Au,
Organometallics 2012, 31, 6642-6651. DOI:/10.1021/om300718k

206
205

S. De, S. Pramanik, M. Schmittel,
Synthesis of Azabipyridine and Azaterpyridine Building Blocks for Multitopic Binding,
Synthesis 2012, 44, 2959-2963. DOI:/10.1055/s-0032-1316749

205
204

M. Lal Saha, S. Pramanik, M. Schmittel,
Spontaneous and Catalytic Fusion of Supramolecules,
Chem. Commun. 2012, 48, 9459 – 9461. DOI:/10.1039/C2CC35036J

Links to a highlight of the above work: http://blogs.rsc.org/cc/2012/08/22/supramolecular-splicing-catalytic-fusion-of-supramolecules/

204
203

S. Khatua, D. Samanta, J. W. Bats, M. Schmittel,
Rapid and Highly Sensitive Dual-Channel Detection of Cyanide by Bis-heteroleptic Ruthenium(II) Complexes,
Inorg. Chem. 2012, 51, 7075–7086. DOI:/10.1021/ic2022853

203
202

M. L. Saha, M. Schmittel,
Degree of Molecular Self-sorting in Multicomponent Systems,
Org. Biomol. Chem. 2012, 10, 4651–4684. DOI:/10.1039/C2OB25098E

202
201

M. Schmittel, S. Qinghai, M. E. Cinar
Tuning the Wavelength of Electrochemiluminescence by Anodic Potential: A Design Using Non-Kekulé-Structured Iridium-Ruthenium Luminophores,
Dalton Trans. 2012, 41, 6064 - 6068, DOI:/10.1039/C2DT30303E

201
200

M. Schmittel, Soumen De, Susnata Pramanik,
A Reversible ON-OFF Nanoswitch for Organocatalysis: Mimicking the Locking-Unlocking Operation of CaMKII,
Angew. Chem. Int. Ed. 2012, 51, 3832 –3836. DOI:/10.1002/ange.201108089
Angew. Chem. 2012, 124, 3898 –3902. DOI:/10.1002/anie.201108089

Highlighted in http://www.rsc.org/chemistryworld/News/2012/March/nanoswitch-controls-organic-Knoevenagel-reaction.asp

200
199

R. Breuer, M. Schmittel,
1,1´-Biferrocenylenes – The More Redox Stable Ferrocenes! New Derivatives, Corrected NMR Assignments, Redox Behavior and Spectroelectrochemistry,
Organometallics 2012, 1870–1878 DOI:/10.1021/om201215w

199
198

M. Schmittel, C. Vavilala, M. E. Cinar,
The Thermal C2-C6 (Schmittel)/Ene Cyclization of Enyne-Allenes – Crossing the Boundary between Classical and Non-Statistical Kinetics,
J. Phys. Org. Chem.2012, 25 182–197. DOI:/10.1002/poc.1887

198
197

M. Schmittel, S. Qinghai,
Lab-on-a-Molecule for Anions in Aqueous Solution: Using Kolbe Electrolysis and Radical Methylation at Iridium for Sensing,
Chem. Commun. 2012, 48, 2707-2709. DOI:/10.1039/C2CC17731E

197
196

196
J. Fan, M. L. Saha, B. Song, H. Schönherr, M. Schmittel,
Preparation of a Poly-Nanocage Dynamer: Correlating the Growth of Polymer Strands Using Constitutional Dynamic Chemistry and Heteroleptic Aggregation,
J. Am. Chem. Soc. 2012, 134, 150–153. DOI:/10.1021/ja209879h

196

 2011      ↑

195

K. Mahata, M. Schmittel,
Impact of the level of complexity in self-sorting: Fabrication of a supramolecular scalene triangle,
Beilstein J. Org. Chem. 2011, 7, 1555–1561. DOI:/10.3762/bjoc.7.183

195
194

G. Eder, S. Kloft, N. Martsinovich, K. Mahata, M. Schmittel, W. M. Heckl, M. Lackinger,
Incorporation Dynamics of Molecular Guests into Two-Dimensional Supramolecular Host Networks at the Liquid-Solid Interface,
Langmuir 2011, 27, 13563–13571. DOI:/10.1021/la203054k

194
193

S. Qinghai, J. W. Bats, M. Schmittel,
Two closely related iridium(III) complexes as colorimetric and fluorometric chemodosimeters for nitrite in aqueous solution operating along different modes of action,
Inorg. Chem. 2011, 50, 10531–10533. DOI:/10.1021/ic201753v

193
192

O. Shekhah, H. K. Arslan, K. Chen, M. Schmittel, R. Maul, W. Wenzel, C. Wöll,
Post-synthetic modification of epitaxially grown, highly oriented functionalized MOF thin films,
Chem. Commun. 2011,47, 11210–11212. DOI: 10.1039/C1CC12543E

192
191

S. K. Samanta, D. Samanta, J. W. Bats, M. Schmittel,
DABCO as a Dynamic Hinge in Cofacial Porphyrin Panels and its Tumbling Inside a Supramolecular Cavity,
J. Org. Chem. 2011, 76, 7466–7473. DOI: 10.1021/jo201252q

191
190

M. Schmittel, M. Lal Saha, J. Fan,
Scaffolding a Cage-Like 3D Framework by Coordination and Constitutional Dynamic Chemistry,
Org. Lett. 2011, 13, 3916–3919. DOI: 10.1021/ol201440a

190
189

A. de los Rios, P. Mal, A. J. Meixner, D. Khoptyar, M. Schmittel,
Fluorescent Chemosensors for Chromium(III) Ions and the Cr3+ / Cr2+ Ratio,
Bull. Chem. Soc. Jpn. 2011, 84, 620-622. DOI: 10.1246/bcsj.20100339

189
188

188
H. Walch, J. Dienstmaier, G. Eder, R. Gutzler, S. Schlögl, K. Das, M. Schmittel, M. Lackinger,
Extended Two-Dimensional Metal-Organic Frameworks Based on Thiolate-Copper Coordination Bonds,
J. Am. Chem. Soc. 2011, 133, 7909–7915. DOI: 10.1021/ja200661s

188
187

187
M. E. Cinar, C. Vavilala, J. Fan, M. Schmittel,
The Thermal C2-C6/[2+2] Cyclisation of Enyne-Allenes: Reversible Diradical Formation,
Org. Biomol. Chem. 2011, 9, 3776 – 3779. DOI: 10.1039/C0OB01275K

187

 2010     ↑

186

K. Mahata, M. Lal Saha, M. Schmittel,
From an 8-Component Self-Sorting Algorithm to a Trisheterometallic Scalene Triangle,
J. Am. Chem. Soc. 2010, 132, 15933–15935. DOI: 10.1021/ja108419k

186

185

J. Völker, X. Zhou, X. Ma, S. Flessau, H. Lin, M. Schmittel, A. Mew,
Semiconductor Nanocrystals with Adjustable Hole Acceptors: Tuning the Fluorescence Intensity by Metal–Ion Binding,
Angew. Chem. Int. Ed. 2010, 49, 6865–6868. DOI: 10.1002/anie.201001441;
Angew. Chem. Int. Ed. 2010, 122, 7017–7020. DOI: 10.1002/ange.201001441

185
184

M. Schmittel, S. K. Samanta,
Orthogonal actuation of a supramolecular double-porphyrin tweezer,
J. Org. Chem. 2010, 75, 5911-5919. DOI: 10.1021/jo101169f

184
183

J. F. Dienstmaier, K. Mahata, H. Walch, W. M. Heckl, M. Schmittel, M. Lackinger,
On the Scalability of Supramolecular Networks – High Packing Density vs. Optimized Hydrogen Bonds in Tricarboxylic Acid Monolayers,
Langmuir 2010, 26, 10708–10716. DOI: 10.1021/la101634w

183
182

C. Vavilala, J. W. Bats, M. Schmittel,
Classical vs. Non-Statistical Behavior in the C2-C6/ene Cyclization of Enyne-Allenes: Intramolecular Kinetic Isotope Effects and Radical Clock Reactions,
Synthesis 2010, 2213 - 2222. DOI:10.1055/s-0029-1218799

182
181

M. Schmittel, K. Mahata,
A fully dynamic five-component triangle via self-sorting,
Chem. Commun. 2010, 46, 4163 - 4165. DOI:10.1039/C0CC00191K

181
180

H. Lin, M. E. Cinar, M. Schmittel,
Comparison of ruthenium(II) and cyclometalated iridium(III) azacrown ether phenanthroline hybrids for the detection of metal cations by electrochemiluminescence
Dalton Trans. 2010, 39, 5130 - 5138. DOI: 10.1039/C000449A
179

S. De, K. Mahata, M. Schmittel,
Metal-coordination-driven dynamic heteroleptic architectures,
Chem. Soc. Rev., 2010, 39, 1555-1575. DOI:10.1039/b922293f

179
178

R. Gutzler, T. Sirtl, J. F. Dienstmaier, K. Mahata, W. M. Heckl, M. Schmittel, M. Lackinger,
Reversible Phase Transitions in Self-Assembled Monolayers at the Liquid-Solid Interface - Temperature Controlled Opening and Closing of Nanopores,
J. Am. Chem. Soc. 2010, 132, 5084-5090. DOI: 10.1021/ja908919r

178
177

M. Schmittel, P. Mal, A. de los Rios,
Multiport logic operations triggered by protonation - a trisphenanthroline as a 3-input AND-NOR-OR circuit,
Chem. Commun. 2010, 46, 2031-2033, DOI: 10.1039/b920959j

177

 2009     ↑

176

G. Li, S. Moreno Flores, C. Vavilala, M. Schmittel, K. Graf,
Evaporation Dynamics of Microdrops on Self-Assembled Monolayers of Dialkyl Disulfides,
Langmuir 2009, 25, 13438-13447. DOI: 10.1021/la901422v

176
175

M. Schmittel, M. Lal, R. Lal, M. Röck, A. Langels, Z. Rappoport, A. Basheer, J. Schlirf, H.-J. Deiseroth, U. Flörke, G. Gescheidt,
A comprehensive picture of the one-electron oxidation chemistry of enols, enolates and a-carbonyl radicals - Oxidation potentials and characterization of radical intermediates,
Tetrahedron 2009, 65, 10842-10855.  doi:10.1016/j.tet.2009.10.039

175
174

K. Mahata, M. Schmittel,
From Twofold Completive to Integrative Self-sorting: a Five-Component Supramolecular Trapezoid,
J. Am. Chem. Soc. 2009, 131, 16544-16554. DOI: 10.1021/ja907185k
free access: http://pubs.acs.org/articlesonrequest/AOR-VBx5Qatepx8vwiKk5B9Z

174

173

M. Schmittel, B. He, J. Fan, J. W. Bats, M. Engeser, M. Schlosser, H.-J. Deiseroth,
Cap for Copper(I) Ions! Metallosupramolecular Solid and Solution State Structures on the Basis of the Dynamic Tetrahedral [Cu(phenAr2)(py)2]+ Motif,
Inorg. Chem. 2009, 48, 8192-8200. DOI: 10.1021/ic900657w

173
172

G. Bucher, A. A. Mahajan, M. Schmittel,
The Photochemical C2-C6 Cyclization of Enyne-Allenes: Interception of the Fulvene Diradical with a Radical Clock Ring Opening,
J. Org. Chem. 2009, 74, 5850-5860. DOI: 10.1021/jo900439x

172
171

J. Fan, J. W. Bats, M. Schmittel,
Combining Dynamic Heteroleptic Complex Formation with Constitutional Dynamic Synthesis - A Facile Way to M3LL’ Cage Assemblies,
Inorg. Chem. 2009, 48, 6338-6340. DOI: 10.1021/ic9008366
http://pubs.acs.org/articlesonrequest/AOR-QXbR8yE9gUD45vuuhibu

171
170

M. Schmittel, K. Mahata,
Multicomponent Assembly of Heterometallic Isosceles Triangles,
Inorg. Chem. 2009, 48,  822-824, DOI: 10.1021/ic8021084

170
169

R. Gutzler, S. Lappe, K. Mahata, M. Schmittel, W. M. Heckl, M. Lackinger,
Aromatic interaction vs. hydrogen bonding in self-assembly at the liquid-solid interface,
Chem. Commun. 2009, 680-682, DOI: 10.1039/b812890a

169

 2008     ↑

168
M. Schmittel, H. Lin,
Transformation of a Modest Luminescent Chemosensor into a Light-up Probe: The Overload Displacement Approach,
Bull. Chem. Soc. Japan. 2008, 81,1595-1598.
DOI:10.1246/bcsj.81.1595
167
T. Linker, D. Schanzenbach, E. Elamparuthi, T. Sommermann, W. Fudickar, V. Gyóllai,  L. Somsák, W. Demuth, M. Schmittel,
The Remarkable Oxidation Stability of Glycals - Excellent Substrates for Cerium(iv)-Mediated Radical Reactions,
J. Am. Chem. Soc. 2008, 130, 16003-16010. DOI: 10.1021/ja8052706
166
G. Bucher, A. A. Mahajan, M. Schmittel,
The Photochemical C2-C6 Cyclization of Enyne-Allenes: Detection of a Fulvene Triplet Diradical in the Laser Flash Photolysis,
J. Org. Chem. 2008, 73, 8815-8828.
165
M. Schmittel, B. He,
Void and filled supramolecular nanoprisms - Notable differences between seemingly identical construction principles,
Chem. Commun. 2008, 4723-4725, DOI: 10.1039/b808988d
164
M. Schmittel, K. Mahata,
Diversity and Complexity Through Reversible Multiple Orthogonal Interactions in Multicomponent Assemblies,
Angew. Chem. Int. Ed. 2008, 47, 5284-5464, DOI: 10.1002/anie.200800583
Vielfalt und Komplexität durch reversible vielfach-orthogonale Wechselwirkungen in Multikomponenten-Systemen,
Angew. Chem. 2008, 120, 5364-5366, DOI: 10.1002/ange.200800583
163
L. Kampschulte, T. L. Werblowsky, R. S. K. Kishore, M. Schmittel, W.M. Heckl, M. Lackinger,
Thermodynamical Equilibrium of Binary Supramolecular Networks at the Liquid-Solid Interface
J. Am. Chem. Soc. 2008, 130, 8502-8507. DOI: 10.1021/ja801883t
162
S. Moreno-Flores, A. Kasry, H.-J. Butt, C. Vavilala, M. Schmittel, D. Pum, U. B. Sleytr, J. L. Toca-Herrera,
From Native to Non-native Two-Dimensional Protein Lattices through Underlying Hydrophilic/ Hydrophobic Nanoprotrusions,
Angew. Chem. 2008, 120, 4785 -4788. DOI: 10.1002/ange.200800151
Angew. Chem. Int. Ed. 2008, 47, 4707-4710. DOI: 10.1002/anie.200800151
161
M. Schmittel, B. He, P. Mal,
Supramolecular Multi-Component Self-Assembly of Shape Adaptive Nanoprisms: Wrapping up C60 with Three Porphyrin Units,
Org. Lett. 2008, 10 (12), 2513-2516. DOI: 10.1021/ol800796h
160
M. Schmittel, K. Mahata,
Clean formation and dynamic exchange reactions of a supramolecular equilateral triangle that is both heterometallic and heteroleptic,
Chem. Commun. 2008, 2550-2552. DOI: 10.1039/b801462k
159
M. Schmittel, J.-P. Steffen, D. Rodríguez, B. Engelen, E. Neumann, M. E. Cinar,
Thermal C2-C6 Cyclisation of Enyne-Carbodiimides: Experimental Evidence Contradicts a Diradical and Suggests a Carbene Intermediate,
J. Org. Chem. 2008, 73, 3005 - 3016 DOI: 10.1021/jo701966h
158
M. Schmittel, P. Mal,
Towards technomimetic spoked wheels: Dynamic hexakis-heteroleptic coordination at a hexakis-terpyridine scaffold,
Chem. Commun. 2008, 960 - 962. DOI: 10.1039/b718185j
157
M. Schmittel, H.-W. Lin,
Electropolymerisable Ruthenium(II) Phenanthrolines Carrying Azacrown Ether Receptors: Metal Ion Recognition in Thin Film Redox Sensors,
J. Mat. Chem. 2008, 18, 333 - 343; DOI:10.1039/b712604b
http://www.rsc.org/ej/JM/2008/b712604b.pdf
156
H. Schäfer, H. Lin, M. Schmittel, M. Böhm,
A labchip for highly selective and sensitive electrochemiluminescence detection of Hg2+ ions in aqueous solution employing integrated amorphous thin film diodes,
Microsyst. Technol. 2008, 14 (4-5), 589-599. DOI: 10.1007/s00542-007-0439-5

 2007     ↑

155
M. Schmittel, H.-W. Lin
Luminescent Iridium Phenanthroline Crown Ether Complex for the Detection of Silver(I) Ions in Aqueous Media
Inorg. Chem. 2007, 46, 9139 - 9145. DOI: 10.1021/ic700413v;
Electronic Reprints
154
M. Schmittel, C. Vavilala, R. Jaquet
Non-statistical dynamic effects before and after the transition state! Intra- versus intermolecular kinetic isotope effects suggest a broad transition state zone
Angew. Chem. 2007, 119, 7036-7039; DOI: 10.1002/ange.200700709
Angew. Chem.Int. Ed. 2007, 46, 6911 -6914. DOI: 10.1002/anie.200700709
153
M. Schmittel, Bice He, V. Kalsani, J. W. Bats
Supramolecular Effects on the Potential of Redox Units - Nanoscaffolds Internally Functionalised with Ferrocene Units
Org. Biomol. Chem. 2007, 5, 2395 - 2403. DOI: 10.1039/b703633g
152
A. Listorti, A. Degli Esposti, R. S. K. Kishore, V. Kalsani, M. Schmittel, N. Armaroli
1,10-Phenanthrolines with tunable luminescence upon protonation: a spectroscopic and computational study
J. Phys. Chem. A 2007, 111; 7707-7718. DOI: 10.1021/jp0723766
151
O. N. Gritsenko, E. A. Gutkina, H. Ammon, M. Schmittel, A. A. Shteinman
New Phenanthroline Iron Complexes: Synthesis and Catalytic Activity in Alkane Oxidation with Hydrogen Peroxide
Russ. J. Inorg. Chem. 2007, 52, 92-96. (Zhurnal Neorganicheskoi Khimii, 2007, 52, 97-102).
150
M. Schmittel, V. Kalsani, C. Michel, P. Mal, H. Ammon, J. P. Rabe, F. Jäckel
Towards Nanotubular Structures with Large Void. Dynamic Heteroleptic Oligophenanthroline Metallo-Nanoscaffolds and Their Solution State Properties
Chem. Eur. J. 2007, 13, 6223-6237. DOI: 10.1002/chem.200700020
149
H. Schäfer, H. Lin, M. Schmittel, M. Böhm
A novel labchip with amorphous thin film diodes used for highly selective and sensitive electrochemiluminescence detection of Hg2+ ions in aqeous solution
Proc. SPIE Microtechnologies for the New Millennium 2007, Maspalomas, Spain, 2-4 May 2007.
148
M. Schmittel, A. Mahajan, G. Bucher, J. W. Bats
Thermal C2-C6 Cyclization of Enyne-Allenes. Experimental Evidence for a Stepwise Mechanism and for an Unusual Thermal Silyl Shift
J. Org. Chem. 2007, 72, 2166-2173. DOI: 10.1021/jo062448+
147
M. Schmittel, H.-W. Lin
Quadruple-Channel Sensing: A Molecular Sensor with One Single Type of Receptor Site for Selective and Quantitative Multiion Analytics
Angew. Chem. 2007, 119, 911-914. DOI: 10.1002/ange.200603362
Angew. Chem. Int. Ed. 2007, 46, 893-896. DOI: 10.1002/anie.200603362
highlighted in Nature: A. P. de Silva, Nature 2007, 445 (7129): 718-719.
146
146
M. Schmittel, R. S. K. Kishore, J. W. Bats
Synthesis of Supramolecular Fullerene-Porphyrin-Cu(phen)2-Ferrocene Architectures. A Heteroleptic Approach Towards Tetrads
Org. Biomol. Chem. 2007, 5, 78 - 86. DOI: 10.1039/b614111k
145
M. Schmittel, M. Strittmatter, A. A. Mahajan, C. Vavilala, M. E. Cinar, M. Maywald
Steric Effects in the Thermal C2-C6 Diradical Cyclization of Enyne-Allene
Arkivoc 2007, Part(viii), 66-84.

 2006     ↑

144
R. S. K. Kishore, T. Paululat, M. Schmittel
From Supramolecular Porphyrin Tweezers to Dynamic AnBmClDk Multiporphyrin Arrangements Through Orthogonal Coordination
Chem. Eur. J. 2006, 12, 8136-8149. DOI: 10.1002/chem.200600463
143
R. S. K. Kishore, V. Kalsani, M. Schmittel
Self-Assembly of a Bis-Porphyrinic Supramolecular Rectangle Using Two Orthogonal Binding Strategies
Chem. Commun. 2006, 3690-3692.
142
M. Schmittel, V. Kalsani, P. Mal, J. W. Bats
The HETTAP Approach: Self-Assembly and Metal Ion Sensing of Dumbbell-Shaped Molecules and Clip Molecules
Inorg. Chem. 2006, 45,  6370-6377. DOI: 10.1021/ic060403l
141
M. Schmittel, H.-W. Lin, E. Thiel, A. J. Meixner, H. Ammon
Redox and Luminescence Investigations of Ruthenium Trisphenanthroline Crown Ether Hybrids upon Multiple Ion Loading
Dalton Trans. 2006, 4020 - 4028; DOI: 10.1039/b605270c
140
S. Moreno Flores, A. Shaporenko, C. Vavilala, H.-J. Butt, M. Schmittel, M. Zharnikov, R. Berger
W. M. Heckl
Control of surface properties of self-assembled monolayers by tuning the degree of molecular asymmetry
Surface Science 2006, 600, 2847-2856. doi:10.1016/j.susc.2006.04.047
139
M. Schmittel, V. Kalsani, F. Jäckel, J. P. Rabe, J. W. Bats, D. Fenske
Rigid Bisphenanthrolines: Synthesis, Structure and Self-Assembly at the Solid-Liquid Interface
Eur. J. Org. Chem. 2006, 3079-3086, DOI: 10.1002/ejoc.200600174
138
S. J. H. Griessl, M. Lackinger, A.-K. Maier, R. S. K. Kishore, L. Kampschulte, M. Schmittel, W. M. Heckl
Solvent Induced Polymorphism of 1,3,5-Benzenetribenzoic Acid on Graphite Surfaces - a New Template Structure
J. Phys. Chem. B 2006, 110, 10829-10836, DOI: 10.1021/jp057553m
137
V. Kalsani, M. Schmittel, A. Listorti, G. Accorsi, N. Armaroli
Novel phenanthroline ligands and their kinetically locked copper(I) complexes with unexpected photophysical properties
Inorg. Chem. 2006, 45, 2061-2067. DOI: 10.1021/ic051828v

 2005     ↑

136
M. Schmittel, M. Lal, K. Graf, G. Jeschke, I. Suske, J. Salbeck
N,N´-Dimethyl-2,3-dialkylpyrazinium Salts as Redox-Switchable Surfactants? Redox, Spectral, EPR and Surfactant Properties
Chem. Comm. 2005, 5650-5652.
135
M. Bennati, F. Lendzian, M. Schmittel, H. Zipse
Spectroscopic and Theoretical Approaches for Studying Radical Reactions in Class I Ribonucleotide Reductase
Biol. Chem. 2005, 386, 1007-1022.
134
M. Schmittel, V. Kalsani, R. S. K. Kishore, H. Cölfen, J. W. Bats
Dynamic and Fluorescent Nanoscale Phenanthroline/Terpyridine Zinc(II) Ladders. Self-Recognition in Unlike Ligand/Like Metal Coordination Scenarios
J. Am. Chem. Soc. 2005, 127, 11545-11546.
133
M. Schmittel, C. Vavilala
Kinetic Isotope Effects in the Thermal C2-C6 Cyclization of Enyne-Allenes: Experimental Evidence Supports a Stepwise Mechanism
J. Org. Chem. 2005, 70, 4865-4868. DOI: 10.1021/jo0504971
132
M. Schmittel, V. Kalsani, J. W. Bats
Metal-Driven and Covalent Synthesis of Supramolecular Grids from Dynamic Racks: A Convergent Approach to Heterometallic and Heteroleptic Nanostructures
Inorg. Chem. 2005, 44, 4115-4117. DOI: 10.1021/ic050088n
131
V. Kalsani, H. Bodenstedt, D. Fenske, M. Schmittel
Supramolecular Copper Phenanthroline Racks: Structures, Mechanistic Insight and Dynamic Nature
Eur. J. Inorg. Chem. 2005, 1841-1849.
130
M. Schmittel, A. A. Mahajan, G. Bucher
Photochemical Myers-Saito and C2-C6-Cyclizations of Enyne-Allenes - Direct Detection of Intermediates in Solution
J. Am. Chem. Soc. 2005, 127, 5324-5325.
129
M. Schmittel, G. Morbach, W. A. Schenk, M. Hagel
Synthesis, Thermal Reactivity and Structure of 1,2-Bis(4-hydroxy-3-methoxyphenylethynyl)benzene
J. Chem. Cryst. 2005, 35, 373-379.
128
M. Schmittel, C. Michel, A. Wiegrefe
Synthesis of Soluble, Linear Trisphenanthrolines - Precursors for the Construction of Heteroleptic Tripledeckers, Nanogrids and Nanoladders
Synthesis 2005, 367 - 373.
127
M. Schmittel, V. Kalsani
Functional, Discrete, Nanoscale Supramolecular Assemblies
Top. Curr. Chem. 2005, 245, 1 - 53.

 2004     ↑

126
H. Schäfer, K. Seibel, M. Walder, L. Schöler, T. Pletzer, M. Waidelich, H. Ihmels, M. Schmittel, D. Ehrhardt, M. Böhm
A Micro Cytometer with Monolithically Integrated Optical Detectors Based on Amorphous Silcon
µTAS, 8th International Conference on Miniaturized Systems for Chemistry and Life Sciences, 2004, 443-445.
125
V. Kalsani, H. Ammon, F. Jäckel, J. P. Rabe, M. Schmittel
Synthesis and Self-Assembly of a Rigid Exotopic Bisphenanthroline Macrocycle: Surface Patterning and a Supramolecular Nanobasket
Chem. Eur. J. 2004, 10, 5481-5492.
124
M. Schmittel, M. Lal, M. Schlosser, H.-J. Deiseroth
A Supramolecular Ladder Motif in 2-(2,2,6,6-Tetramethylpiperidin-1-yloxy)propane-1,3-diol
Acta Cryst. C, 2004, C60, o589-o591.
123
M. Schmittel, V. Kalsani, L. Kienle
Simple and Supramolecular Copper Complexes as Precursors in the HRTEM Induced Formation of Crystalline Copper Nanoparticles
Chem. Commun. 2004, 1534-1535.
122
M. Schmittel, R.S.K Kishore
Tetrakis-heteroleptic complexation at porphyrins: a convenient route to diversely functionalised aggregates
Org. Lett. 2004, 6, 1923-1926.
121
M. Schmittel, V. Kalsani, D. Fenske, A. Wiegrefe,
Self-Assembly of Heteroleptic [2x2] and [2x3] Nanogrids,
Chem. Comm. 2004, 490-491.
120
M. Schmittel, A. Mahajan, J.-P. Steffen,
A New Facile Synthesis of exo-Methylene 3,1-Benzothiazines,
Synthesis, 2004, 415-418.

 2003     ↑

119
A. Haeuseler, W. Henn, M. Schmittel,
Stereoselective Assembly of Three Different Carbonyl Components by Two Successive Aldol Reactions Using Group IVa and IVb Metals,
Synthesis, 2003, 2576-2589.
118
M. Schmittel, M. Lal, W. A. Schenk, M. Hagel, N. Burzlaff, A. Langels,
Synthesis and One-Electron Oxidation Chemistry of Stable ß,ß-Dimesityl Enols with Heteroaryl Substituents,
Z. Naturforschg. B, 2003, 58b, 877-884.
117
M. Schmittel, M. Lal, M. Schlosser, H.-J. Deiseroth,
Unusual ladder like supramolecular arrangement by cooperative effect of bifurcated O-H…O hydrogen bonding in crystals of racemic 4-ferrocenylbutan-1,2-diol,
CrystEngComm., 2003, 5, 294-299.
116
M. Lal, A. Langels, H.-J. Deiseroth, J. Schlirf, M. Schmittel,
The Role of Hydrogen Bonding in the Oxidation Potential of Enols,
J. Phys. Org. Chem. 2003, 16, 373-379.
115
M. Schmittel, A. Haeuseler,
Access to Unsymmetric Binaphthols Through Oxidative Coupling of Silicon Bisnaphtholates,
Z. Naturforschg. B, 2003, 58b, 211 - 216.
114
M. Schmittel, G. Viola, F. Dall'Acqua, G. Morbach
A Novel Concept to Activate Enediynes for DNA Cleavage
Chem. Commun.2003, 646 - 647.
113
M. Schmittel, A. Haeuseler, T. Nilges, A. Pfitzner
The Elusive Aldol Reaction of Enolates with Aldolates - A Highly Stereoselective Process Using Three Different Carbonyl Components
Chem. Commun.,2003, 34 - 35

 2002     ↑

112
M. Schmittel, A. Haeuseler
One-Electron Oxidation of Metal Enolates and Metal Phenolates
J. Organomet. Chem.2002,661, 169-179.
111
M. Schmittel, H. Ammon, V. Kalsani, A. Wiegrefe, C. Michel
Quantitative Formation and Clean Metal Exchange Processes of Large Void (> 5000 Å3) Nanobox Structures,
Chem. Commun.2002, 2566 - 2567.
110
M. Schmittel, A. Haeuseler,
Elektronentransfer Reaktionen von Metallenolaten und -phenolaten
in Elektronenübertragung in Chemie und Biochemie, Hrsg. J. Russow, H. J. Schäfer, S. 31 - 37, GDCh, Frankfurt, 2002.
109
M. Schmittel, A. Ganz, D. Fenske,
Ring-in-Ring Structures from Phenanthroline Macrocycles with Exo and Endotopic Binding Sites,
Org. Lett., 2002,4, 2289 - 2292.
108
 M. Oelgemöller, A. Haeuseler, M. Schmittel, A. G. Griesbeck, J. Lex, Y. Inoue
Hydrogen Bonding in Phthalimido Carboxylic Acids: Cyclic Voltammography Study and Correlation with Photochemical Reactivity. Part 2. Aliphatic and Aromatic Acids,
Perkin Trans. 2,2002, 676 - 686.

 2001     ↑

107
M. Schmittel, M. K. Ghorai
Aldolases as leitmotif – a nonenzymatic domino aldol reaction triggered by zinc bisenolate and polyenolate (ate) complexes,
Synlett 2001, 1992-1994.
106
C. Michel, D. Habibi, M. Schmittel
3-(4-Iodo-phenylethynyl)-[1,10]phenanthroline
Molecules, 2001, 6, M226
105
C. Michel, D. Habibi, M. Schmittel
3-Ethynyl-[1,10]phenanthroline
Molecules, 2001, 6, M225
104
C. Michel, D. Habibi, M. Schmittel
3-Trimethylsilanylethynyl-[1,10]phenanthroline
Molecules, 2001, 6, M224
103
M. Schmittel, C. Michel, A. Wiegrefe, V. Kalsani
Synthesis of Soluble, Linear Bisphenanthrolines for the Construction of Heteroleptic NanoGrids and Nanoboxes.
Synthesis, 2001, 1561 – 1567.
102
M. Schmittel, J.-P. Steffen, M. Maywald, B. Engels, H. Helten, P. Musch
Ring Size Effects in the C2-C6 Biradical Cyclisation of Enyne-Allenes and the Relevance for Neocarzinostatin.
Perkin Trans. 2, 2001, 1331-1339.
101
M. Schmittel, G. Morbach, B. Engelen, M. Panthöfer
Unexpected host-guest interactions of a novel V-shaped enediyne and water molecules.
CrystEngComm, 2001, 32.
100
M. Schmittel, K. Peters, E.-M. Peters, A. Haeuseler, H. Trenkle
Radical Cation Ester Cleavage in Solution. The Mechanism of the Mesolytic O-CO Bond Scission.
J. Org. Chem., 2001, 66, 3265 - 3276.
99
M. Oelgemöller, A. G. Griesbeck, J. Lex, A. Haeuseler, M. Schmittel, M. Niki, D. Hesek, Y. Inoue
Structural, Cyclic Voltammetric and IR-Spectral Evidences for Preorientation in PET-Active Phthalimido Carboxylic Acids,
Org. Lett.,, 2001, 3, 1593-1596.
98
A. G. Griesbeck, M. Oelgemöller, J. Lex, A. Haeuseler, M. Schmittel
Synthesis of Sulfur-Containing Macrocyclic Ring Systems via Photoinduced Decarboxylative Cyclization
Eur. J. Org. Chem., 2001, 1831-1843.
97
M. Schmittel, C. Michel, S.-X. Liu, D. Schildbach, D. Fenske
New Sterically Encumbered 2,9-Diarylphenanthrolines for the Selective Formation of Heteroleptic Copper(I) Bisphenanthroline Complexes
Eur. J. Inorg. Chem., 2001, 1155 - 1166
96
S. Hünig, A. Langels, M. Schmittel, H. Wenner, I. F. Perepichka, K. Peters
Violene/Cyanine Hybrids as Electrochromic Systems. A New Variation of the General Structure
Eur. J. Org. Chem., 2001, 1393 - 1399.
95
M. Schmittel, M. K. Ghorai
Reactivity Patterns of Radical Ions - A Unifying Picture of Radical-anion and Radical-cation Transformations
in Electron Transfer in Chemistry, Ed. V. Balzani, Vol. 2 (Organic Molecules, Organometallic and Inorganic Molecules), p. 5-54, Wiley-VCH, 2001.
94
M. Schmittel, M. Maywald
Electronic effects in the thermal C2-C6 biradical cyclisation of enyne-allenes
Chem. Commun., 2001, 155-156.

 2000     ↑

93
M. Schmittel, D. Rodríguez, J.-P. Steffen
Synthesis and Photochemical Cyclization of a Novel Enyne-Carbodiimide
Molecules, 2000, 5, 1372-1378.
92
S.-X. Liu, C. Michel, M. Schmittel
A Highly Regioselective Sonogashira Coupling as a Key Step in the Preparation of the First Phenanthroline with Two Diverse Reactive Groups in 3,8-Positions
Organic Lett. 2000, 2, 3959-3962.
91
R. Söllner, T. Koy, M. Schmittel
(u,l,l,u)-3,5-Diethyl-2,4,6-triphenyltetrahydropyran-2,4-diol
Molecules, 2000, 5, M176.
90
M. Schmittel, R. Söllner, K. Drauz, K. Günther
Tetrahydropyran-2,4-diols, Method for producing them and their use
WO 20000 27 836
89

M. Schmittel, D. Rodríguez, J.-P. Steffen
A Highly Efficient Triplet Analogue of a Thermal Biradical Cyclization - the Photochemical C2-C6 Cyclization of Enyne-heteroallenes
Angew. Chem. 2000, 112, 2236-2239.
88
M. Schmittel, R. Söllner, K. Drauz, K. Günther
Tetrahydropyran-2,4-diole, Verfahren zu deren Herstellung und Verwendung
DE 199 111 98
87
M. Schmittel, A. Ganz, D. Fenske, M. Herderich
Heteroleptic Silver(I) and Zinc(II) Bisphenanthroline Complexes
J. Chem. Soc., Dalton Trans. 2000, 353-359.

 1999     ↑

86
A. Burghart, M. Schmittel, M. Keller
Structures of two sterically crowded molecular propeller systems
J. Chem. Crystallogr. 1999, 29, 421-427.
85
M. Schmittel, J.-P. Steffen, A. Burghart
First Characterization of Phosphoenol Radical Cations in Solution and the Kinetics of the Mesolytic P-O Bond Cleavage in Sterically Shielded Enoxy-Phosphorous Compounds after One-Electron Oxidation
Acta Chem. Scand. 1999, 53, 781-791.
84
R. Herges, F. Starck, T. Winkler, M. Schmittel
Quadricyclane Radical Cation Isomerizations
Chem. Eur. J. 1999, 5, 2965-2970.
83
M. Schmittel, M. K. Ghorai, A. Haeuseler, W. Henn, T. Koy, R. Söllner
Stereoselective Synthesis of Tetrahydropyran-2,4-diols via a Simple Domino-Aldol-Aldol-Hemiacetal One-Pot-Reaction
Eur. J. Org. Chem. 1999, 2007-2010.
82
M. Schmittel, H. Ammon
Preparation of a Rigid Macrocycle with Two Exotopic Phenanthroline Binding Sites
Synlett 1999, 750 - 752.
81
M. Schmittel, A. Burghart, H. Werner, M. Laubender, R. Söllner
Probing M-O Bond Cleavage in Silicon and Titanium Bisenolate Radical Cations
J. Org. Chem., 1999, 64, 3077 - 3085
80
M. Schmittel, A. Ganz, W. A. Schenk, M. Hagel
Synthesis and Coordination Properties of 6,6'-Dimesityl-2,2'-bipyridine
Z. Naturforsch. B, 1999, 559 - 563
79
M. Schmittel, C. Michel, A. Ganz, M. Herderich
Synthesis of Macrocyclic Phenanthrolines with Exotopic Binding Sites. Probing Their Complexation Behavior with Copper(I) and Iron(II)
J. Prakt. Chem., 1999, 341, 228 - 236
78
M. Schmittel, R. Söllner
Zirconium Enolate Radical Cations in Solution - Characterisation and Kinetics of Their Mesolytic Zr-O Bond Cleavage
Perkin Trans. 2, 1999, 515
77
H. Werner, M. Laubender, M. Schmittel, R. Söllner
Crystal structure of Chloro-di-h5-cyclopentadienyl-[1,1-dimesityl-3,3-dimethylbut-1-en-2-oxy]titan, C34H41ClOTi
Z. Kristallogr., 1999, NCS 214, 47 - 48

 1998     ↑

76
M. Schmittel, M. Strittmatter, W.A. Schenk, M. Hagel
Benzo[b]fluorenes Formed in the Thermal Cyclization of 3-Ene-1,6-diynes
Z. Naturforsch., 1998, 53b, 1015-1020
75
M. Schmittel, M. Strittmatter,
Cyclization of Carbonyl Substituted Enyne-Allenes: C2-C6-Cyclization
Induced by Heat or by Addition of Samarium(ll) Iodide, Samarium(Ill)
Chloride, or Boron Trifluoride
Tetrahedron 1998, 54, 1375-13760. 
74
M. Schmittel, A. Langels
Enol radical cations in solution. Part 13. First Example of a Radical Dication Rearrangement. One-Electron Oxidation of Dihydrobenzofuranyl Cations Leads to Drastic Rate Enhancement in the Oxidative Benzofuran Formation from Enols 
J. Org. Chem., 1998, 63, 7328-7337
73
M. Schmittel, J.-P. Steffen, B. Engels, C. Lennartz, M. Hanrath
Two level thermal biradical cyclizations in theory and experiment. New synthetic routes to 6H-inolo[2,3-b]quinolines and 2-aminoquinolines from enyne-carbodiimides
Angew. Chem., 1998, 110, 2531-2533; Angew. Chem. Int. Ed., 1998, 37, 2371-2373
72
T. Linker, M. Schmittel
(Buch) Radikale und Radikalionen in der Organischen Synthese, Wiley-VCH, 420 S., Weinheim, 1998
71
K. L. Double, M. Maywald, M. Schmittel, P. Riederer, M. Gerlach
In vitro studies of ferrilin iron release and neurotoxicity
J. Neurochem., 1998, 2492-2499
70
B. Engels, C. Lennartz, M. Hanrath, M. Schmittel, M. Strittmatter
Comparing two competing biradicyl cyclizations in enyne-allenes: Influence of substituents on the switch from the Myers-Saito to the novel C2-C6 cyclization
Angew. Chem., 1998, 110, 2067-2070; Angew. Chem. Int. Ed. Engl., 1998, 37, 1960-1963
69
I. Kovacik, O. Gevert, H. Werner, M. Schmittel, R. Söllner
Study of the relative p-acceptor ability ofunsaturatedligands:C(=C)nPh2(n=0, 1, 2 and 4) based on cyclic valtammetry of complexes trans-[RhCl(L)PiPr3)2] (L= :C(=C)nPh2, C2H4 and CO)
Inorg. Chim. Acta, 1998, 275-276, 435-439
68
M. Schmittel, J.-P. Steffen, M. A. Wencesla Angel, B. Engels, C. Lennartz, M. Hanrath
Two novel thermal biradical cyclizations of synthetic importance in enyne-ketenimines. Theory and experiment.
Angew. Chem., 1998, 110, 1633-1635; Angew. Chem. Int. Ed. Engl., 1998, 37, 1562-1564 DOI: 10.1002/(SICI)1521-3757(19980605)110:11<1633::AID-ANGE1633>3.0.CO;2-Z
67
M. Schmittel, H. Ammon
A Short Synthetic Route to 4,7-Dihalogenated 1,10-Phenanthrolines With Additional Groups in 3,8-Position: Soluble Precursors for Macrocyclic Oligophenanthrolines
Eur. J. Org. Chem., 1998, 785-792 DOI: 10.1002/(SICI)1099-0690(199805)1998:5<785::AID-EJOC785>3.0.CO;2
66
M. Schmittel, M. Keller, A. Burghart, Z. Rappoport, A. Langels
Electronic effects in polyarylvinyl propellers. Solid state structures and dynamic behaviour in solution of several crowded enol derivatives
Perkin Trans. 2, 1998, 869-875 DOI: 10.1039/a707906k
65
M. Schmittel, R. Söllner
First Characterization of Zirconium Enolate Radical Cations in Solution and Their Mesolytic Bond Cleavage to Zirconocene Cations
Chem. Commun., 1998, 565-566  DOI: 10.1039/a708495a
64
M. Schmittel, A. Langels
Enol radical cations in solution. Part 12. Synthesis and electrochemical investigations of a stable enol linked to a ferrocene redox centre
Perkin Trans. 2, 1998, 565 - 572 DOI: 10.1039/a707743b
63
M. Schmittel, A. Burghart, W. Malisch, J. Reising, R. Söllner
Diastereoselective Enolate Coupling through Redox Umpolung in Silicon and Titanium Bisenolates - a Novel Concept Based on Intramolecularization of Carbon Carbon Bond Formation
J. Org. Chem., 1998, 63, 369 - 400  DOI: 10.1021/jo971650x
62
A. Burghart, A. Haeuseler, A. Langels, R. Söllner, M. Schmittel
One-Electron Oxidation of Metal Enolates
in Selective Reactions of Metal Activated Molecules, Hrsg, H. Werner, P. Schreier, Vieweg Verlag, 1998, 73-78
61
K. Peters, E.-M. Peters, M. Schmittel and H. Trenkle
Crystal structure of 2-acetoxy-1,1dimesityl-3,3-dimethylbut-1-ene, C26H34O2
Zeitschr. Krist., 1998, 105-106

 1997     ↑

60
M. Schmittel, U. Lüning, M. Meder, A. Ganz, C. Michel, M. Herderich
Synthesis of Sterically Encumbered 2,9-Diaryl Substituted Phenantrolines. Key Building Blocks for the Preparation of Mixed (Bis-Heteroleptic) Phenanthroline Copper(I) Complexes
Heterocycl. Commun., 1997, 3; 493-498
59
M. Schmittel, A. Burghart
Understanding Reactivity Patterns of Radical Cations
Angew. Chem., 1997, 109, 2659-2699; Angew. Chem. Int. Ed. Engl., 1997, 36, 2550-2589 DOI:10.1002/ange.19971092304
58
M. Schmittel, J.-P. Steffen, I. Bohn
Domino Reaction Cascades to Heteroarene fused Benzofluorenes from Enediyne Alcohols: [2,3]-Sigmatropic Rearrangement or SN2-Reaction Followed by a Thermal C2-C6-Biradical Cyclization
Heterocycl. Commun., 1997, 3, 443
57
M. Schmittel, G. Gescheidt, L. Eberson, H. Trenkle
Persistent Benzofuran Radical Cations in Solution. A Cyclic Voltammetry and EPR/ENDOR Study
Perkin Trans. 2, 1997, 2145-2150 DOI:10.1039/a704594h
56
K. Peters, E.-M. Peters, M. Schmittel and H. Trenkle
Crystal structure of 1,1-dimesityl-3,3-dimethyl-2-trifluoroacetoxybut-1-ene, C26H31O2F3
Zeitschr. Krist., 1997, 467-468
55
M. Schmittel, H. Ammon
A Short Synthetic Route to Novel, Highly Soluble 3,8-Dialkyl-4,7-dibromo-1,10-phenanthrolines
Synlett, 1997, 1096-1098 DOI: 10.1055/s-1997-1525
54
M. Schmittel, J.-P. Steffen, D. Auer, M. Maywald
Ring Strain Effects in Enyne-Allene Thermolysis: Switch from the Myers-Saito Reaction to the C2-C6 Biradical Cyclization
Tetrahedron Lett., 1997, 6177-6180 DOI:10.1016/S0040-4039(97)01393-2
53
M. Schmittel, S. Kiau
Electron Transfer versus Acid Catalysis in Enediyne Cyclizations,
Liebigs Ann., 1997, 1391-1399 DOI:10.1002/jlac.199719970716
52
M. Schmittel, A. Ganz
Synthesis of 4,7-Disubstituted Phenanthrolines as Key Building Blocks for the First Preparation of Macrocyclic Mono- and Bisphenanthrolines with exo-Coordination Sites
Synlett, 1997, 710-711  DOI: 10.1055/s-1997-3243
51
M. Schmittel, A. Ganz
Stable mixed phenanthroline copper(I) complexes. Key building blocks for supramolecular coordination chemistry
Chem. Commun., 1997, 999-1000 DOI:10.1039/a701509g
50
M. Schmittel, R. Söllner
Titanium Enolate Radical Cations in Solution: Generation, Characterization and their Reactions
Chem. Ber., 1997, 130, 771-777 DOI:10.1002/cber.19971300616
49
M. Schmittel, M. Keller, S. Kiau, M. Strittmatter
A Surprising Switch from the Myers-Saito Cyclization to a Novel Biradical Cyclization in Enyne-Allenes. Formal Diels-Alder and Ene Reactions with High Synthetic Potential
Chem. Eur. J., 1997, 3, 807 - 816  DOI:10.1002/chem.19970030521
48
M. Schmittel, H. Trenkle
First characterisation of enol carbonate and enol carbamate radical cations in solution. Kinetics and selectivity of the mesolytic cleavage of the O-CO bond
Chem. Lett., 1997, 299 - 300 DOI:10.1246/cl.1997.299
47
M. Schmittel, S. Kiau
First Isolation of two Rotamers about the P-C Bond in a Phosphine Oxide
Liebigs Ann./Recueil, 1997, 733 - 736 DOI:10.1002/jlac.199719970415
46
M. Schmittel, C. Wöhrle, I. Bohn
Radical Cation Initiated Cycloaddition of Electron-Rich Allenes. Evidence for a Stepwise Mechanism
Acta Chem. Scand., 1997, 51, 151-157 DOI:10.3891/acta.chem.scand.51-0151
45
M. Schmittel, M. Maywald and M. Strittmatter
Synthesis of Novel Enyne-Allenes, Their Thermal C2-C6 Cyclization, and the Importance of a Benzofulvene Biradical in the DNA Strand Cleavage
Synlett, 1997, 165-166  DOI:10.1055/s-1997-726
44
M. Schmittel, H. Werner, O. Gevert and R. Söllner
Sterically Shielded Titanocene Enolates. Synthesis, Structure and their Exceptional Stability against Hydrolysis
Chem. Ber., 1997, 130, 195 - 199
43
M. Schmittel, A. Langels
A Shortlived Radical Dication as a Key Intermediate in the Rearrangement of a Persistent Cation. The Oxidative Cyclization of 2,2-Dimesityl-1-(4-N,N-dimethylaminophenyl)ethenol
Angew. Chem., 1997, 109, 381 - 383; Angew. Chem., Int. Ed. Engl., 1997, 36, 392 -295 DOI:10.1002/anie.199703921

1996     ↑

42

M. Schmittel, H. Trenkle
Mesolytic O-CO Bond Cleavage versus Intramolecular Cyclization Reaction in Enol Trifluoroacetate Cation Radicals. A Kinetic and Mechanistic Investigation
J. Chem. Soc., Perkin Trans. 2, 1996, 2401 - 2406  DOI:10.1039/P29960002401
41
M. Schmittel, J.-P. Steffen, A. Burghart
One-Electron Oxidation of Enol Phosphates, Enol Phosphites and Enol Phosphinates. Evidence for an Unprecedented P-O Bond Cleavage in Phosphoenol Radical Cations in Solution.
Chem. Commun., 1996, 2349 - 2350. DOI:10.1039/CC9960002349
40
M. Schmittel, S. Kiau, T. Siebert, M. Strittmatter
Steric Effects in Enyne-Allene Thermolyses: Switch from the Myers-Saito Reaction to the C2-C6-Cyclization and DNA Strand Cleavage
Tetrahedron Lett., 1996, 37, 7691 - 7694 DOI:10.1016/0040-4039(96)01758-3
39
M. Schmittel, R. Söllner
First Characterization of a Titanium Enolate Cation Radical in Solution. Carbon-Carbon Bond Formation and the Kinetics of the Mesolytic Ti-O Bond Cleavage
Angew. Chem., 1996, 108, 2248 - 2250; Angew. Chem. Int. Ed. Engl., 1996, 35, 2107 - 2109 DOI:10.1002/anie.199621071
38
M. Schmittel, M. Strittmatter, S. Kiau
An Unprecedented Biradical Cyclization as an Alternative Pathway to the Myers-Saito Cycloaromatization in the Thermal Reactions of Enyne Allenes
Angew. Chem., 1996, 108, 1952 - 1954 DOI:10.1002/anie.199618431
37
M. Schmittel, C. Wöhrle, I. Bohn
The Aminium Salt and Photoinduced Electron Transfer Initiated Diels-Alder Cycloaddition of Electron-Rich Allenes. Evidence for a Stepwise Mechanism and the Importance of Steric and Electronic Effects for the Reactivity of Distonic Cation Radical Intermediates
Chem. Eur. J., 1996, 2, 1031 - 1040 DOI: 10.1002/chem.19960020820
36
M. Schmittel, A. Langels
Synthesis and One-Electron Oxidation Chemistry of Novel, Stable Conjugated Dienols and Yne-Enols,
Liebigs Ann., 1996, 999 - 1004
35
M. Schmittel, M. Levis
Electron Transfer Induced Deprotection of Benzyl Substituted 1,3-Dithianes with Iron(III)phenanthroline Complexes
Synlett, 1996, 315 - 316 DOI: 10.1055/s-1996-5412
34
M. Schmittel, M. Strittmatter, K. Vollmann, S. Kiau
Intramolecular Formal Diels-Alder Reactions in Enyne Allenes. A New Synthetic Route to Benzofluorenes and Indeno[1,2-g]-quinolines
Tetrahedron Lett., 1996, 37, 999 - 1002  DOI:10.1016/0040-4039(95)02369-0

 1995     ↑

33

M. Schmittel, H. von Seggern
Aminium Salt Initiated Oxygenation of Ketenes. - Formation of Succinic Anhydrides
Liebigs Ann., 1995, 1815 - 1821 DOI: 10.1002/jlac.1995199510254
32
M. Schmittel, M. Strittmatter and S. Kiau
Switching from the Myers-Saito-Reaction to a New Thermal Cylization Mode in Enyne-Allenes,
Tetrahedron Lett., 1995, 36, 4975 - 4978 DOI: 10.1016/0040-4039(95)00937-8
31
M. Schmittel, A. Burghart and M. Keller
Silyl Enol Ether Cation Radicals in Solution: Nucleophile Assisted Si-O Bond Cleavage,
J. Chem. Soc., Perkin Trans. 2, 1995, 2327 - 2333 DOI:10.1039/P19950002327
30
M. Schmittel, C. Wöhrle
The Cation Radical Catalyzed Diels-Alder Reaction of Electron Rich Allenes
J. Org. Chem., 1995, 60, 8223 - 8230 DOI:10.1021/jo00130a022
29
M. Schmittel, H. Ammon, C. Wöhrle
Tris(1,10-phenanthroline)iron(II) Complexes. Broad Variation of the Redox Potential by 4,7-Substitution at the Phenanthroline Ligands
Chem. Ber., 1995, 128, 845 - 850 DOI:10.1002/cber.19951280816
28
M. Schmittel, J. Heinze, H. Trenkle
Mesolytic Cleavage of the O-CO Bond in Enol Acetate Cation Radicals with Direct Formation of a-Carbonyl Cations. Mechanistic and Synthetic Aspects.
J. Org. Chem., 1995, 60, 2726-2733 DOI: 10.1021/jo00114a020
27
S. Kiau, M. Schmittel
Polar Effects in the Transition State of the Bergman Cyclization
Chem. Lett., 1995, 953 - 954 DOI:10.1246/cl.1995.953
26
M. Schmittel and H. Ammon
Synthesis and Spectroscopy of New Iron(II) Complexes of 4,7-Bis(aza-crown ether)-Phenanthrolines with Unusual Complexation Properties
J. Chem. Soc., Chem. Commun., 1995, 687-688 DOI: 10.1039/C39950000687
25
M. Keller, H. von Seggern, M. Schmittel, C. Wöhrle
Crystal structures of (endo, anti)-5-ethylidene-1,2,3,4,6,7-hexamethyl-6-(4-methoxyphenyl)-bicyclo[2.2.1]-hept-2-ene (C22H30O) and (endo, anti)-1,3,4,5,6,7-hexamethyl-3-(4-methoxyphenyl)-bicycyclo[2.2.1]hept-5-en-2-one (C20H26O2)
Zeitschr. Krist., 1995, 210, 602-604

1994     ↑
24
M. Schmittel, M. Levis
a-Umpolung of Ketones and Aldehydes via the Corresponding Silyl Enol Ether Cation Radicals,
Chem. Lett., 1994, 1939 - 1940. DOI:10.1246/cl.1994.1939
23
M. Schmittel, M. Levis
a-Umpolung of Ketones via Enol Cation Radicals, Mechanistic and Synthetic Aspects,
Chem. Lett., 1994, 1935 - 1938 DOI:10.1246/cl.1994.1935
22
M. Schmittel, G. Gescheidt, M. Röck
Erste spektroskopische Identifizierung eines Enol-Radikalkations in Lösung: Das Anisyldimesitylethenol-Radikalkation
Angew. Chem., 1994, 106, 2056-2058; Angew. Chem. Int. Ed. Engl., 1994, 33, 1961 - 1963 DOI: 10.1002/anie.199419611
21
H. von Seggern, M. Schmittel
Acid Induced Stereoselective Formation of Cyclohepta-3,5-dienones from Ketenes and Dienes
Chem. Ber., 1994, 127, 1269 - 1274 DOI:10.1002/cber.19941270715
20

M. Levis, U. Lüning, M. Müller, M. Schmittel, C. Wöhrle
Tris(1,10-phenanthroline)iron(II) Complexes. Influence of 4,7-Donor Substitution on the Redox Potential
Z. Naturforsch., 1994, 49b, 675-682
19
M. Röck, M. Schmittel
A new efficient Synthesis of 4,6,7-Trimethylbenzofurans by oxidation of ß-mesityl substituted Enols,
J. Prakt. Chem., 1994, 336, 325-329 DOI:10.1002/prac.19943360409
18
M. Schmittel
a-Umpolung of Ketones via Enol Radical Cations,
Top. Curr. Chem., 1994, 169, 183-230

1993     ↑
17
M. Schmittel, C. Wöhrle
Electron Transfer Initiated Diels-Alder Reaction with Allenes as Dienophiles
Tetrahedron Lett., 1993, 34, 8431-8434
16
M. Röck, M. Schmittel
a-Carbonyl Cation Chemistry from Enolate Oxidation
J. Chem. Soc., Chem. Commun., 1993, 1739-1741 DOI: 10.1039/C39930001739
15
E.A. Nadler, M. Röck, M. Schmittel, Z. Rappoport
Relative Stability of Crowded Isomeric Enols: 2-Mesityl-2-phenyl-ethenols and Their Methyl Ethers,
J. Phys. Org. Chem., 1993, 6, 233-242 DOI: 10.1002/poc.610060407
14
M. Schmittel, H. von Seggern
Ketene - Diene [4+2] Cycloaddition Products via Cation Radical Initiated Diels-Alder Reaction or Vinylcyclobutanone Rearrangement,
J. Am. Chem. Soc., 1993, 115, 2165-77 DOI: 10.1021/ja00059a010

1992     ↑
13
G. Gescheidt, A. Lamprecht, J. Heinze, M. Schmittel, S. Kiau, C. Rüchardt
Electron Transfer Catalyzed Cis --> Trans Isomerization of 1,1'-Azonorbornane. Prototype of a Reversible two-Stage Storage System
Helv. Chim. Acta, 1992, 75, 1607-1611 DOI: 10.1002/hlca.19920750515
12
M. Schmittel, M. Röck
Enol Cation Radicals in Solution, 3. - Reaction of Enol Cation Radicals in the Presence of Nucleophiles,
Chem. Ber., 1992, 125, 1611-1620
11
E.K.A. Wolber, M. Schmittel, C. Rüchardt
Neue Synthesen für isomerenreine Allyl- und Propargylcyanide durch Isocyanid-Cyanid-Umlagerung,
Chem. Ber., 1992, 125, 525-531

1991      ↑

10
G. Gescheidt, A. Lamprecht, C. Rüchardt, M. Schmittel
Radical Cations and Radical Anions of Three Bridgehead Azopolycycloalkanes: - A Fluid-Solution ESR Study
Helv. Chim. Acta, 1991, 74, 2094-2099
9
M. Schmittel, H. von Seggern
Durch Ammoniumylsalze initiierte Diels-Alder Reaktion von Ketenen- Steuerung der [2+2]- vs. [4+2]-Selektivität,
Angew. Chem., 1991, 103, 981-983; Angew. Chem. Int. Ed. Engl., 1991, 30, 999-1001 DOI:10.1002/anie.199109991

1990     ↑
8
M. Schmittel, A. Abufarag, O. Luche, M. Levis
a-Umpolung von Ketonen über Enol-Radikalkationen, eine mechanistische Studie
Angew. Chem., 1990, 102, 1174-1176; Angew. Chem. Int. Ed. Engl., 1990, 29, 1144-1146 DOI: 10.1002/anie.199011441
7
M. Schmittel, U. Baumann
Stabilität und Cyclisierung von Enol-Radikalkationen, eine mechanistische Studie zur Einelektronenoxidation von ß,ß-Dimesitylenolen,
Angew. Chem., 1990, 102, 571 - 572 DOI: 10.1002/ange.19901020524
Angew. Chem. Int. Ed. Engl., 1990, 29, 541-543 DOI: 10.1002/anie.19900541

1989     ↑

1988     ↑
6
J.P. Dinoocenzo, M. Schmittel
Dioxygen-Promoted Cation Radical Reactions in Bronsted Acids
J. Org. Chem., 1988, 53, 4145

1987     ↑
5
M. Schmittel, C. Rüchardt
Stereoisomerization and Homolytic Decomposition of cis- and trans- Bridgehead Azocompounds
J. Am. Chem. Soc., 1987, 109, 2750-2759
4
J.P. Dinnocenzo, M. Schmittel
Cyclopropane Stereomutation Catalyzed by One-Electron Oxidants
J. Am. Chem. Soc., 1987, 109, 1561-1562 DOI:10.1021/ja00239a042

1986      ↑

3
W. Bernlöhr, M.A. Flamm-ter Meer, J.H. Kaiser, M. Schmittel, H.-D. Beckhaus, C. Rüchardt
Cis- and trans-Tetracyclopropyl- and Tetra-tert-butyl azomethanes
Chem. Ber., 1986, 119, 1911-1918 DOI:10.1002/cber.19861190613

1985     ↑
2
R. van Eldik, H. Kelm, M. Schmittel, C. Rüchardt
Concerning the Mechanism of Isomerization of cis-Azoalkanes
J. Org. Chem., 1985, 50, 2998-3000 DOI:10.1021/jo00216a039

1984     ↑

1983     ↑

1982     ↑

1981     ↑
1
M. Schmittel, A. Schulz, C. Rüchardt, E. Hädicke
Cis- and trans 1-Azonorbornane
Chem. Ber., 1981, 114, 3533-3548 DOI:10.1002/cber.19811141107

  Statistik     ↑

Zeitschrift

Zahl der Veröffentlichungen
ACS Nano 3
Acta Chem. Scand. 2
Acta Cryst. C 1
Adv. Inorg. Chem.
1
Analyst 3
Anal. Bioanal. Chem.
1
Angew. Chem. 27              
Angew. Chem. Int. Ed. 24              
ARKIVOC 1
Beilstein J. Org. Chem. 6
Biol. Chem. 1
Bull. Chem. Soc. Japan. 2
Chem. Ber. 8
Chem. Commun. / J. Chem. Soc.
45
Chem. Eur. J. 8
Chem. Lett. 4
Chemistry 1
Chem. Mat. 1
ChemistryOpen
1
Chem. Rec.  1
Chem. Rev.
1
Chem. Soc. Rev. 2
Coord. Chem. Rev.
1
CrystEngComm 2
Dalton Trans.
13
Eur. J. Org. Chem. 6
Eur. J. Inorg. Chem. 2
 Foundations of Science 1
Helv. Chim. Acta 2
Heterocycl. Commun. 2
Inorg. Chem. 21              
Inorg. Chim. Acta 1
Israel J. Chem
1
J. Am. Chem. Soc.      22              
J. Chem. Crystallogr. 1
J. Mat. Chem. 1
J. Neurochem. 1
J. Org. Chem. 23 
J. Organomet. Chem 1
J. Phys. Chem. A 1
J. Phys. Chem. B 1
J. Phys. Org. Chem. 5
J. Prakt. Chem. 2
Langmuir 6
Liebigs Ann. / Liebigs Ann./Recueil 4
Macromol. Chem. Phys.
1
Microsyst. Technol. 1
Molecules 6
Monatsh. Chem.
1
Nano Lett. 1
Nanoscale
2
NanoscaleHorizons 1
Org. Biomol. Chem. 8
Organic Lett. 13
Organometallics 3
Perkin Trans. 2
8
Phys. Chem. Chem. Phys
2
RSC Adv. 2
Russ. J. Inorg. Chem. 1
Supramol. Chem.
1
Surface Science 1
Synlett 6
Synthesis 6
Tetrahedron 3
Tetrahedron Lett. 5
Top. Curr. Chem. 2
Z. Naturforsch. 4
Zeitschr. Krist. 3
Aktualisiert via XIMS am 3.5.2023 von E. Cinar
 
Suche
Hinweise zum Einsatz der Google Suche