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首页> 外文期刊>Beilstein journal of organic chemistry. >TTFs nonsymmetrically fused with alkylthiophenic moieties
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TTFs nonsymmetrically fused with alkylthiophenic moieties

机译:TTF与烷基噻吩部分不对称融合

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Two new dithiolene ligand precursors, containing fused TTF and alkyl thiophenic moieties 3,3'-{[2-(5-(tert-butyl)thieno[2,3-d][1,3]dithiol-2-ylidene)-1,3-dithiole-4,5-diyl]bis[sulfanediyl]}dipropanenitrile (α-tbtdt, 1), and 3,3'-{[2-(5-methylthieno[2,3-d][1,3]dithiol-2-ylidene)-1,3-dithiole-4,5-diyl]bis[sulfanediyl]}dipropanenitrile (α-mtdt, 2), were synthesized and characterized. The electrochemical properties of these electronic donors were studied by cyclic voltammetry (CV) in dichloromethane. Both compounds show two quasi-reversible oxidation processes, versus Ag/AgCl, typical of TTF donors at E11/2 = 279 V and E21/2 = 680 V for 1 and E11/2 = 304 V and E21/2 = 716 V in the case of 2. The single-crystal X-ray structure of 1 and of a charge transfer salt of 2, (α-mtdt)[Au(mnt)2] (3), are reported.
机译:两种新的二硫代烯配体前体,包含稠合的TTF和烷基噻吩部分3,3'-{[2-(5-(叔丁基)硫代[2,3-d] [1,3]二硫代-2-亚烷基]- 1,3-二硫代-4,5-二基]双[硫代二基]}二丙腈(α-tbtdt,1)和3,3'-{[2-(5-methylthieno [2,3-d] [1,合成并表征了3]二硫醇-2-亚基)-1,3-二硫醇-4,5-二基]双[硫代二基]}二丙腈(α-mtdt,2)。这些电子给体的电化学性质通过在二氯甲烷中的循环伏安法(CV)进行了研究。与Ag / AgCl相比,这两种化合物均表现出两个准可逆的氧化过程,这是典型的TTF供体在1时E11 / 2 = 279 V和E21 / 2 = 680 V时以及E11 / 2 = 304 V和E21 / 2 = 716 V时发生的。在2的情况下。报道了1的单晶X射线结构和2的电荷转移盐(α-mtdt)[Au(mnt)2](3)。

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