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Publikationen nach Koautoren

Publikationen / Publications

Prof. Dr. Michael Schmittel

sortiert nach Mitautoren / ordered by coauthors

A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Ammon, H.
Biswas, Pronay Kumar
Bodenstedt, H.
Breuer, R.
Burghart, A.
Chen, K.
Cinar, E.
Das, K.
de los Rios, Alejandra
De, Soumen
Demuth, W.
Fan, J.
Gaikwad, S.
Ganz, A.
Ghorai, M. K.
Ghosh, A.
Goswami, A.
Habibi, D.
Haeuseler, A.
He, Bice
Henn, W.
Kalsani, V.
Khatua, S.
Kiau, S.
Kishore, R.S.K.
Koy, T.
Lal, M.
Lal Saha, M.
Langels, A.
Levis, M.
Lin, H.-W.
Liu, S.-X.
Mahajan, A.
Mahata, K.
Mal, P.
Maywald, M.
Michel, C.
Mittal, N.
Morbach, G.
Nanaji, Yerramsetti
Natarajan, P.
Neogi, S.
Qinghai, S.
Özer, Merve Sinem
Paul, Indrajit
Pramanik, Susnata
Rana, Anup
Röck, M.
Saha, S.
Samanta, D.
Samanta, S. K.
Söllner, R.
Steffen, J.-P.
Strittmatter, M.
Trenkle, H.
Vavilala, C.
von Seggern, H.
Wiegrefe, A.
Wöhrle, C.

Veröffentlichungen gemeinsam mit Horst Ammon (10) ↑

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

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

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

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

82
M. Schmittel, H. Ammon
Preparation of a Rigid Macrocycle with Two Exotopic Phenanthroline Binding Sites
Synlett 1999, 750 - 752.

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.

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.

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.

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.
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).

Veröffentlichungen gemeinsam mit Pronay Kumar Biswas (7) ↑

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

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

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

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

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

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

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

Veröffentlichungen gemeinsam mit Heinrich Bodenstedt (1) ↑

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.

Veröffentlichungen gemeinsam mit Rochus Breuer (6) ↑

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

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

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

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

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

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

Veröffentlichungen gemeinsam mit Armin Burghart (9) ↑

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

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.

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

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

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

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

81
M. Schmittel, A. Burghart, H. Werner, M. Laubender, R. Söllner
Silicon and Titanium Bisenolate Radical Cations in Solution - Sequential M-O Bond Cleavage upon One-Electron Transfer Activation
J. Org. Chem., 1999, 64, 3077 - 3085

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.

86
A. Burghart, M. Schmittel, M. Keller
Structures of two sterically crowded molecular propeller systems
J. Chem. Crystallogr. 1999, 29, 421-427.

Veröffentlichungen gemeinsam mit Kun Chen (9) ↑

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

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

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

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

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

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/

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

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

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

Veröffentlichungen gemeinsam mit Emin Cinar (15) ↑

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.

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

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

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

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

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

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

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

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

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

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

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

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

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: dx.doi.org/10.1007/s00706-016-1841-4

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

Veröffentlichungen gemeinsam mit Kalpataru Das (3)

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

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

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

Veröffentlichungen gemeinsam mit Wolfgang Demuth (1) ↑

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

Veröffentlichungen gemeinsam mit Alejandra de los Rios (2) ↑

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

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

Veröffentlichungen gemeinsam mit Soumen De (15) ↑

179
S. De, K. Mahata, M. Schmittel,
Metal-coordination-driven dynamic heteroleptic architectures,
Chem. Soc. Rev., 2010, 39, 1555-1575. DOI:10.1039/b922293f

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

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

209
M. Schmittel, S. Pramanik, S. De,
A Reversible Nanoswitch as ON/OFF Photocatalyst,
Chem. Commun. 2012, 48, 11730-11732. DOI:/10.1039/C2CC36408E

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

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

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

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

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

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

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

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

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

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

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

Veröffentlichungen gemeinsam mit Jian Fan (6) ↑

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

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

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

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

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

Veröffentlichungen gemeinsam mit Sudhakar Gaikwad (7)

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

267
S. Gaikwad, M. Schmittel,
Five-State Rotary Nanoswitch,
J. Org. Org. Chem. 2017, 82, 343–352. DOI:/10.1021/acs.joc.6b02436

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

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

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

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

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: dx.doi.org/10.1039/c9ob01456j

Veröffentlichungen gemeinsam mit Andrea Ganz (7)

51
M. Schmittel, A. Ganz
Stable mixed phenanthroline copper(I) complexes. Key building blocks for supramolecular coordination chemistry
Chem. Commun., 1997, 999-1000

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

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

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.

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

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.

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.

Veröffentlichungen gemeinsam mit Manas K. Ghorai (3) ↑

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.

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.

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.

Veröffentlichungen gemeinsam mit Amit Ghosh (4) ↑

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

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

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

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

Veröffentlichungen gemeinsam mit Abir Goswami (8) ↑

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

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

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

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

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

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

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

Veröffentlichungen gemeinsam mit Davood Habibi (3) ↑

104
C. Michel, D. Habibi, M. Schmittel
3-Trimethylsilanylethynyl-[1,10]phenanthroline
Molecules, 2001, 6, M224

105
C. Michel, D. Habibi, M. Schmittel
3-Ethynyl-[1,10]phenanthroline
Molecules, 2001, 6, M225

106
C. Michel, D. Habibi, M. Schmittel
3-(4-Iodo-phenylethynyl)-[1,10]phenanthroline
Molecules, 2001, 6, M226

Veröffentlichungen gemeinsam mit Andreas Haeuseler (11) ↑

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.

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.

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.

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.

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.

112
M. Schmittel, A. Haeuseler
One-Electron Oxidation of Metal Enolates and Metal Phenolates
J. Organomet. Chem. 2002, 661, 169-179.

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.

115
M. Schmittel, A. Haeuseler,
Access to Unsymmetric Binaphthols Through Oxidative Coupling of Silicon Bisnaphtholates,
Z. Naturforschg. B, 2003, 58b, 211 - 216.

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.

Veröffentlichungen gemeinsam mit Bice He (4)

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.

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

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

Veröffentlichungen gemeinsam mit Wolfgang Henn (2)

Veröffentlichungen gemeinsam mit Venkateshwarlu Kalsani (17) ↑

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.

121
M. Schmittel, V. Kalsani, D. Fenske, A. Wiegrefe,
Self-Assembly of Heteroleptic [2x2] and [2x3] Nanogrids,
Chem. Comm. 2004, 490-491.

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.

127
M. Schmittel, V. Kalsani
Functional, Discrete, Nanoscale Supramolecular Assemblies
Top. Curr. Chem. 2005, 245, 1 - 53.

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.

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

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.

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

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

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

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.

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.20070002.

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.

Veröffentlichungen gemeinsam mit Snehadrinarayan Khatua (2)

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

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

Veröffentlichungen gemeinsam mit Susanne Kiau (9)

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

27
S. Kiau, M. Schmittel
Polar Effects in the Transition State of the Bergman Cyclization
Chem. Lett., 1995, 953 - 954

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

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

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

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

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

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

53
M. Schmittel, S. Kiau
Electron Transfer versus Acid Catalysis in Enediyne Cyclizations,
Liebigs Ann., 1997, 1391-1399

Veröffentlichungen gemeinsam mit Ravuri Kishore (8)

122
M. Schmittel, R. S. K. Kishore,
Tetrakisheteroleptic complexation at porphyrins: a convenient route to diversely functionalised aggregates,
Org. Lett. 2004, 6, 1923-1926.

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

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.

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

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

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

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

Veröffentlichungen gemeinsam mit Thomas Koy (2) ↑

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.

Veröffentlichungen gemeinsam mit Mukul Lal (8) ↑

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.

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.

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.

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.

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.

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

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

Veröffentlichungen gemeinsam mit Rupali Lal (1) ↑

Veröffentlichungen gemeinsam mit Manik Lal Saha, (14) ↑

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

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

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

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/

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

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

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

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

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

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

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

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

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

Veröffentlichungen gemeinsam mit Anja Langels (10)

36
M. Schmittel, A. Langels
Synthesis and One-Electron Oxidation Chemistry of Novel, Stable Conjugated Dienols and Yne-Enols,
Liebigs Ann., 1996, 999 - 1004

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

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

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

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.

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.

Veröffentlichungen gemeinsam mit Michael Levis (5) ↑

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

20
M. Levis, U. Lüning, M. Müller, M. Schmittel, C. Wöhrle
Tris(phenanthroline)iron(II) Complexes. Influence of 4,7-Donor Substitution on the Redox Potential
Z. Naturforsch., 1994, 49b, 675-682

23
M. Schmittel, M. Levis
a-Umpolung of Ketones via Enol Cation Radicals, Mechanistic and Synthetic Aspects,
Chem. Lett., 1994, 1935 - 1938

24
M. Schmittel, M. Levis
a-Umpolung of Ketones and Aldehydes via the Corresponding Silyl Enol Ether Cation Radicals,
Chem. Lett., 1994, 1939 - 1940.

35
M. Schmittel, M. Levis
Electron Transfer Induced Deprotection of Benzyl Substituted 1,3-Dithianes with Iron(III)phenanthroline Complexes
Synlett, 1996, 315 - 316

Veröffentlichungen gemeinsam mit Hengwei Lin (8)

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.

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

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

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

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

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

Veröffentlichungen gemeinsam mit Shi-Xia Liu (2)

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.

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.

Veröffentlichungen gemeinsam mit Atul Mahajan (6)

120
M. Schmittel, A. Mahajan, J.-P. Steffen,
A New Facile Synthesis of exo-Methylene 3,1-Benzothiazines,
Synthesis, 2004, 415-418.

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.

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.

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+

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.

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

Veröffentlichungen gemeinsam mit Kingsuk Mahata (13) ↑

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

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

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

170
M. Schmittel, K. Mahata,
Multicomponent Assembly of Heterometallic Isosceles Triangles,
Inorg. Chem., 2009, 48, 822-824, DOI:10.1021/ic8021084

174
K. Mahata, M. Schmittel,
From Twofold Completive to Integrative Self-sorting: a Five-Component Supramolecular Trapezoid,
2009,131, 16544-16554.DOI: 10.1021/ja907185k
free access: http://pubs.acs.org/articlesonrequest/AOR-VBx5Qatepx8vwiKk5B9Z

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

179
S. De, K. Mahata, M. Schmittel,
Metal-coordination-driven dynamic heteroleptic architectures,
Chem. Soc. Rev., 2010, 39, 1555-1575. DOI: 10.1039/b922293f

181
M. Schmittel, K. Mahata,
A fully dynamic five-component triangle via self-sorting,
Chem. Commun. 2010, 46, 4163 - 4165. DOI:10.1039/C0CC00191K

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

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

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

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

Veröffentlichungen gemeinsam mit Prasenjit Mal (6)

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

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/b718185

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

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

Veröffentlichungen gemeinsam mit Michael Maywald (6) ↑

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

54
M. Schmittel, J.-P. Steffen, D. Auer, M. Maywald
Ring Strain Effects in Enyne-Allene Themolysis: Switch from the Myers-Saito Reaction to the C2-C6 Biradical Cyclization
Tetrahedron Lett., 1997, 6177-6180

71
K. L. Double, M. Maywald, M. Schmittel, P. Riederer, M. Gerlach
J. Neurochem., 1998, 2492-2499
In vitro studies of ferritin iron release and neurotoxicity, 1998, 2492-2499

94
M. Schmittel, M. Maywald
Electronic effects in the thermal C²-C⁶ biradical cyclisation of enyne-allenes
Chem. Commun., 2001, 155-156.

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.

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.

Veröffentlichungen gemeinsam mit Christoph Michel (11)

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.

104
C. Michel, D. Habibi, M. Schmittel
3-Trimethylsilanylethynyl-[1,10]phenanthroline
Molecules, 2001, 6, M224

105
C. Michel, D. Habibi, M. Schmittel
3-Ethynyl-[1,10]phenanthroline
Molecules, 2001, 6, M225

106
C. Michel, D. Habibi, M. Schmittel
3-(4-Iodo-phenylethynyl)-[1,10]phenanthroline
Molecules, 2001, 6, M226

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.

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

Veröffentlichungen gemeinsam mit Nikita Mittal (9) ↑

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

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

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

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

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

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

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

Veröffentlichungen gemeinsam mit Guido Morbach (4) ↑

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.

114
M. Schmittel, G. Viola, F. Dall'Acqua, G. Morbach
A Novel Concept to Activate Enediynes for DNA Cleavage
Chem. Commun. 2003, 646 - 647.

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.

Veröffentlichungen gemeinsam mit Yerramsetti Nanaji (1) ↑

Veröffentlichungen gemeinsam mit Palani Natarajan (3) ↑

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

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!

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

Veröffentlichungen gemeinsam mit Sudahip Neogi (5) ↑

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

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 Tempe¬rature: Hydrogen Bonds vs. Metal Coordination in Trinitrile Monolayers,
J. Am. Chem. Soc. 2013, 135, 691–695. DOI:/10.1021/ja306834a

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

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

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

Veröffentlichungen gemeinsam mit Shu Qinghai (6) ↑

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

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

201
M. Schmittel, S. Qinghai,
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

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

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

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

Veröffentlichungen gemeinsam mit Merve Sinem Özer (5) ↑

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

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

Veröffentlichungen gemeinsam mit Indrajit Paul (14) ↑

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

275
D. Samanta, I. Paul, M. Schmittel,
Supramolecular five-component nano-oscillator,
Chem. Commun. 2017, 53, 9709-9712.
DOI: /10.1039/C7CC05235

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

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

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

Veröffentlichungen gemeinsam mit Susnata Pramanik (16) ↑