2,5-BIS(1,4-DITHIAFULVEN-6-YL) FURANS, THIOPHENES AND N-METHYL PYRROLES AS EXTENDED ANALOGS OF TETRATHIAFULVALENE

被引：60

作者：

BENAHMEDGASMI, AS

FRERE, P

GARRIGUES, B

GORGUES, A

JUBAULT, M

CARLIER, R

TEXIER, F

机构：

[1] UNIV ANGERS,CHIM ORGAN FONDAMENTALE & APPL LAB,2 BD LAVOISIER,F-49045 ANGERS,FRANCE

[2] UNIV ORAN,CHIM ORGAN LAB,ORAN,ALGERIA

[3] UNIV SABATIER,SYNTH MOLEC PHOSPHOREES LAB,F-31062 TOULOUSE,FRANCE

[4] UNIV RENNES 1,ELECTROCHIM LAB,F-35042 RENNES,FRANCE

来源：

TETRAHEDRON LETTERS | 1992年 / 33卷 / 43期

关键词：

PI-DONORS; TETRATHIAFULVALENE; (TTF); ANALOGS; ORGANIC CONDUCTORS; WITTIG(-HORNER) REACTIONS; FURANS; THIOPHENES AND N-METHYL-PYRROLES DERIVATIVES; CYCLIC VOLTAMMETRY; THIN LAYER CYCLIC VOLTAMMETRY;

D O I：

10.1016/S0040-4039(00)79014-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The title compounds are synthesized by Wittig or Wittig-Horner reactions between the corresponding furan, thiophen and N-methyl-pyrrole-2,5-dicarbaldehydes and P-reagents W or P bearing the 1,3-dithiol-2-ylidene moiety adequately substituted al the 4,5-positions; thanks to usual and thin layer cyclic voltammetry, they are shown to possess good pi-donor abilities.

引用

页码：6457 / 6460

页数：4

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