Literature DB >> 27003243

Thieno[2,3-b]indole-Based Small Push-Pull Chromophores: Synthesis, Structure, and Electronic Properties.

François Baert1, Clément Cabanetos1, Magali Allain1, Virginie Silvestre1, Philippe Leriche1, Philippe Blanchard1.   

Abstract

Small push-pull molecules were synthesized in high yields by connecting a N-methyl or N-phenyl substituted thieno[2,3-b]indole electron-donating block directly to a 2,2-dicyanovinyl or (1-(dicyanomethylene)-3-oxo-1-inden-2-ylidene)methyl electron-withdrawing group. The effects of the N-substitution on thieno[2,3-b]indole and the nature of the electron-accepting group on the electrochemical, optical, and charge-transport properties were investigated by cyclic voltammetry, UV-vis spectroscopy, and the space-charge-limited current method, respectively. These results, together with the 1% power conversion efficiency of a bilayer solar cell prepared with the smallest compound of the series, show the potential of thieno[2,3-b]indole for organic electronics.

Entities:  

Year:  2016        PMID: 27003243     DOI: 10.1021/acs.orglett.6b00438

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  One-pot multicomponent synthesis of thieno[2,3-b]indoles catalyzed by a magnetic nanoparticle-supported [Urea]4[ZnCl2] deep eutectic solvent.

Authors:  The Thai Nguyen; Phuong Hoang Tran
Journal:  RSC Adv       Date:  2020-03-06       Impact factor: 4.036

2.  Synthesis and Pharmacological Studies of Unprecedented Fused Pyridazino[3',4':5,6][1,2,4]triazino[3,4-b][1,3,4]thiadiazine Derivatives.

Authors:  Rania S Ali; Hosam A Saad
Journal:  Molecules       Date:  2018-04-27       Impact factor: 4.411

3.  3-Alkynylindoles as Building Blocks for the Synthesis of Electronically Tunable Indole-Based Push-Pull Chromophores.

Authors:  Kübra Erden; Cagatay Dengiz
Journal:  J Org Chem       Date:  2022-03-01       Impact factor: 4.354

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.