Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF

被引：6
作者：
Ertas, Erdal [1 ]
Demirtas, Ilknur [1 ]
Ozturk, Turan [2 ,3 ]
机构：
[1] TUBITAK Marmara Res Ctr, FI, TR-41470 Gebze, Turkey
[2] Istanbul Tech Univ, Dept Chem, Fac Sci, Organ Chem, TR-34469 Istanbul, Turkey
[3] TUBITAK UME, Chem Grp Labs, TR-41470 Gebze, Turkey
来源：
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2015年 / 11卷
关键词：
bis(ethylenedithio)tetrathiafulvalene; bis(vinylenedithio)tetrathiafulvalene; tetrathiafulvalene; PI-ELECTRON DONORS; TETRATHIAFULVALENE DERIVATIVES; FUNCTIONALIZED TETRATHIAFULVALENES; ELECTROCHEMICAL PROPERTIES; ORGANIC SUPERCONDUCTORS; LAWESSONS REAGENT; BUILDING-BLOCKS; CHEMISTRY; 1,8-DIKETONES; SALTS;
D O I：
10.3762/bjoc.11.46
中图分类号：
O62 [有机化学];
学科分类号：
070303 ; 081704 ;
摘要：
This review aims to give an overview of the current status of our research on the synthesis of pi-electron donor bis(ethylenedithio) tetrathiafulvalene (BEDT-TTF, ET) analogues prepared from 1,8-diketones via a ring forming reaction. The new synthesized pi-electron donors have vinyl moieties producing extended pi-electron delocalization over the substituent phenyl rings at the peripheries.
引用
收藏
页码：403 / 415
页数：13
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