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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2023 Volume 33, Issue 3, Pages 393–396 (Mi mendc407)

This article is cited in 4 papers

Communications

NIR-absorbing donor–acceptor molecules based on fused thienopyrroloindole

I. V. Dyadishcheva, A. V. Bakirovab, S. M. Peregudovaac, S. A. Ponomarenkoa, Yu. N. Luponosova

a N.S. Enikolopov Institute of Synthetic Polymeric Materials, Russian Academy of Sciences, Moscow, Russian Federation
b National Research Centre 'Kurchatov Institute', Moscow, Russian Federation
c A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation

Abstract: Two novel aromatic compounds containing thieno[2',3':4,5]-thieno[3,2-b]thieno[2' ' , 3' ':4' ,5']thieno[2',3':4,5]-pyrrolo[3,2-g]indole as the electron-donating center and terminal 3-(dicyanomethylene)indan-1-one (or 5,6-difluoro analogue) electron-accepting groups exhibit efficient light absorption in the red and near-infrared spectral regions, have low levels of the highest occupied molecular orbital (up to –5.65 eV) and lowest unoccupied molecular orbital (–3.91 eV) and a relatively low band gap value (up to 1.74 eV). The optical, thermal and structural properties are explored and compared with those of their closest and well known analogues, Y5 and Y6.

Keywords: fused heteropolycyclic compounds, thieno[2',3':4,5]thieno[3,2-b]thieno[2'',3'':4',5']thieno[2',3':4,5]pyrrolo[3,2-g]indole, 3-(dicyanomethylene)indan-1-one, organic dyes, NIR-absorbing compounds, non-fullerene acceptors, donor–acceptor compounds, structural properties.

Language: English

DOI: 10.1016/j.mencom.2023.04.030



© Steklov Math. Inst. of RAS, 2025