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Aqad E, Leriche P, Mabon G, et al. Novel D-pi-A chromophores based on the fulvene accepting moiety. Org Lett. 2001;3(15):2329-32doi: 10.1021/ol016143n.
Aqad, E., Leriche, P., Mabon, G., Gorgues, A., & Khodorkovsky, V. (2001). Novel D-pi-A chromophores based on the fulvene accepting moiety. Organic letters, 3(15), 2329-32. https://doi.org/10.1021/ol016143n
Aqad, E, et al. "Novel D-pi-A chromophores based on the fulvene accepting moiety." Organic letters vol. 3,15 (2001): 2329-32. doi: https://doi.org/10.1021/ol016143n
Aqad E, Leriche P, Mabon G, Gorgues A, Khodorkovsky V. Novel D-pi-A chromophores based on the fulvene accepting moiety. Org Lett. 2001 Jul 26;3(15):2329-32. doi: 10.1021/ol016143n. PMID: 11463308.
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Org Lett. 2001 Jul 26;3(15):2329-32. doi: 10.1021/ol016143n.

Novel D-pi-A chromophores based on the fulvene accepting moiety.

Organic letters

E Aqad, P Leriche, G Mabon, A Gorgues, V Khodorkovsky

Affiliations

  1. Ingénierie Moléculaire et Matériaux Organiques, UFR Sciences, Université d'Angers, 49045 Angers, France.

PMID: 11463308 DOI: 10.1021/ol016143n

Abstract

[reaction: see text] Novel D-pi-A chromophores based on the fulvene accepting moiety and p-dimethylamino phenyl and 1,3-dithiole-2-ylidene donor moieties have been prepared. The X-ray structures of two representative derivatives have been determined. Examination of the UV-visible spectra and cyclic voltamperometry data revealed remarkable sensitivity of the electronic structure of these derivatives to substituents at the cyclopentadiene ring.

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