J
Jean Paul Gisselbrecht
Researcher at University of Strasbourg
Publications - 10
Citations - 573
Jean Paul Gisselbrecht is an academic researcher from University of Strasbourg. The author has contributed to research in topics: HOMO/LUMO & Cycloaddition. The author has an hindex of 9, co-authored 10 publications receiving 513 citations. Previous affiliations of Jean Paul Gisselbrecht include Centre national de la recherche scientifique.
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Journal ArticleDOI
1,1‐Dicyano‐4‐[4‐(diethylamino)phenyl]buta‐1,3‐dienes: Structure–Property Relationships
Francesca Tancini,Yi Lin Wu,W. Bernd Schweizer,Jean Paul Gisselbrecht,Corinne Boudon,Peter D. Jarowski,Marten T. Beels,Ivan Biaggio,François Diederich +8 more
TL;DR: In this paper, a series of 1,1- dicyano-4-[4-(diethylamino)phenyl]buta-1,3-dienes were synthesized and the number and position of additional CN substituents along the 1, 1-dicyanobuta 1,3dienyl fragment was systematically varied.
Journal ArticleDOI
Ambipolar organic transistors and near-infrared phototransistors based on a solution-processable squarilium dye
Paul H. Wöbkenberg,John G. Labram,Jean-Marie Swiecicki,Ksenia Parkhomenko,Dušan N. Sredojević,Jean Paul Gisselbrecht,Dago M. de Leeuw,Donal D. C. Bradley,Jean Pierre Djukic,Thomas D. Anthopoulos +9 more
TL;DR: In this paper, the suitability of a family of solution-processable zwitterionic molecules, so-called squarilium dyes, for the fabrication of organic ambipolar transistors and their application in (opto)electronic circuits is examined.
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Structural, optical, and electrochemical properties of three-dimensional push-pull corannulenes.
Yi Lin Wu,Mihaiela C. Stuparu,Corinne Boudon,Jean Paul Gisselbrecht,W. Bernd Schweizer,Kim K. Baldridge,Jay S. Siegel,François Diederich +7 more
TL;DR: NMR, X-ray, and computational studies on 5 and 8 with one cyanobutadienyl substituent suggested the formation of intermolecular corannulene dimers.
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New donor–acceptor chromophores by formal [2+2] cycloaddition of donor-substituted alkynes to dicyanovinyl derivatives
Peter D. Jarowski,Yi Lin Wu,Corinne Boudon,Jean Paul Gisselbrecht,Maurice Gross,W. Bernd Schweizer,François Diederich +6 more
TL;DR: Electrochemical studies show that the CT properties of these systems are readily tunable by substitution on the electrophile, which has the largest effect on the lowest unoccupied molecular orbital (LUMO).
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Proaromaticity: organic charge-transfer chromophores with small HOMO-LUMO gaps
Yi Lin Wu,Filip Bureš,Peter D. Jarowski,W. Bernd Schweizer,Corinne Boudon,Jean Paul Gisselbrecht,François Diederich +6 more
TL;DR: The NICS results, together with the bond-length analysis of the quinoid spacers, provide strong support that proaromaticity, that is, aromatized zwitterionic mesomeric contributions in the ground state, is effective.