Your browser doesn't support javascript.
loading
3,4-Bisthiolated Pyrroles: Concise Construction and Their Electronic Properties.
Tian, Jun; Feng, Kai; Yuan, Kang-Ning; Li, Xing; Chang, Hong-Hong; Gao, Wen-Chao.
Afiliação
  • Tian J; College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.
  • Feng K; College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.
  • Yuan KN; College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.
  • Li X; College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.
  • Chang HH; College of Biomedical Engineering, Taiyuan University of Technology, Taiyuan 030024, China.
  • Gao WC; Shanxi Tihondan Pharmaceutical Technology Co. Ltd., Jinzhong 030600, China.
J Org Chem ; 87(5): 2402-2409, 2022 03 04.
Article em En | MEDLINE | ID: mdl-35076233
3,4-Bisthiolated pyrroles constitute key cores in pyrrole-based semiconductors, and their electronic properties could be improved by the bisthio groups via the S-effect. Herein, a convenient method for the synthesis of 3,4-bisthiolated pyrroles has been developed through the AlCl3-catalyzed thiolation/cyclization of homopropargylic azides, and cyclic voltammetry and DFT calculations indicated that the desired 3,4-bisthiolated pyrroles had higher HOMO orbital energies and lower band gaps than the parent unsubstituted 2,5-diphenylpyrrole.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirróis / Eletrônica Idioma: En Revista: J Org Chem Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pirróis / Eletrônica Idioma: En Revista: J Org Chem Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China País de publicação: Estados Unidos