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Corinne Boudon

Researcher at University of Strasbourg

Publications -  147
Citations -  5049

Corinne Boudon is an academic researcher from University of Strasbourg. The author has contributed to research in topics: Cycloaddition & Acceptor. The author has an hindex of 42, co-authored 147 publications receiving 4709 citations. Previous affiliations of Corinne Boudon include ETH Zurich & Centre national de la recherche scientifique.

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1,1‐Dicyano‐4‐[4‐(diethylamino)phenyl]buta‐1,3‐dienes: Structure–Property Relationships

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.
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Donor-substituted 1,1,4,4-tetracyanobutadienes (TCBDS): new chromophores with efficient intramolecular charge-transfer interactions by atom-economic synthesis.

TL;DR: Donor-substituted TCBDs are stable molecules and can be sublimed without decomposition and should become interesting chromophores for ultra-thin film formation by vapor deposition techniques and have applications in opto-electronic devices.
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A new class of organic donor–acceptor molecules with large third-order optical nonlinearities

TL;DR: The quite small chromophores are characterised by X-ray crystallography and feature intense intramolecular charge-transfer bands, substantial quinoid character in the donor rings, reversible electrochemical reductions and oxidations and powerful third-order optical nonlinearities.
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Macrocyclization on the fullerene core: Direct regio‐ and diastereoselective multi‐functionalization of [60]fullerene, and synthesis of fullerene‐dendrimer derivatives

TL;DR: In this article, a bis-functionalization method for the double Bingel reaction with optically active bis-malonate derivatives was proposed, which allowed the diastereoselective preparation of optically-active fullerene derivatives and, ultimately, the enanti-lective extraction of higher cyclopropanated adducts.
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Property tuning in charge-transfer chromophores by systematic modulation of the spacer between donor and acceptor.

TL;DR: Degenerate four-wave mixing experiments reveal high third-order optical nonlinearities, pointing to potentially interesting applications of some of the new chromophores in optoelectronic devices.