Elaboration of low-band-gap π-conjugated systems based on thieno[3,4-b]pyrazines

Author:

Cheminet Nathalie1,Nogueira Sandra L.1,Benaqqa Oumayma2,El Malki Zakaria2,Bourass Mohamed3,Cassegrain Simon1,Hamidi Mohammed2,Bouachrine Mohammed3,Sotiropoulos Jean Marc4,Miqueu Karinne4,Jarrosson Thibaut1ORCID,Niebel Claude1,Lère-Porte Jean-Pierre1,Serein-Spirau Françoise1

Affiliation:

1. Institut Charles-Gerhardt de Montpellier, UMR CNRS 5253, Architectures Moléculaires et Matériaux Nanostructurés, Ecole Nationale Supérieure de Chimie de Montpellier , 8 rue de l’Ecole Normale, 34296 Montpellier , Cedex 5 , France

2. Faculté des sciences et techniques , BP 8509, Boutalamine , Errachidia , Morocco

3. ESTM, (LASMAR), University Moulay Ismaïl , Meknes , Morocco

4. Université de Pau et des Pays de l’Adour, UMR5254 – IPREM, Equipe Chimie-Physique , Hélioparc, Pau , France

Abstract

Abstract In order to understand the electronic contribution of the thienopyrazine building block on the electronic properties of π-conjugated systems, small molecules containing thiophene and thienopyrazine moieties are synthesized and jointly studied by theoretical (DFT) and experimental methods (UV-Vis, UPS). Taking advantages of these preliminar attractive results, four low band gap extended structures have been elaborated on the base of Donor-Acceptor-Donor sequences (DAD); these elongated π-conjugated molecules exhibit noticeable electronic and absorption properties spreading from the near UV to NIR regions.

Publisher

Walter de Gruyter GmbH

Subject

General Chemical Engineering,General Chemistry

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