Molecular Complex of [60]Fullerene with 2-(4-thione-l,3-dithiolan-5-yliden)-4,5-dimethyl-1,3-diselenol [C60·2(DTDS)]: Synthesis, Crystal Structure and Properties

N. Spitsina, S. V. Konovalikhin, A. Lobach, E. Golubev, M. Kaplunov, O. A. D’yachenko
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Abstract

Abstract New molecular complexes of [60]fullerene with 2-(4-thione-l,3-dithiolan-5-yliden)-4,5-dimethyl-l,3-diselenol [C60·2(DTDS)] have been synthesized, crystal structure, IR spectral and electrochemical properties have been studied. Partial charge transfer has been found. An unusual shortening of the endocyclic S-C(sp2) bond in the DTDS molecule has been found to be stipulated by conformational vibrations of the >CH2 group. A comparative analysis of the X-ray data for the [C60·2(DTDS)] crystals and the quantum chemical calculations (SCF MO, 6-31G* basis) for the DTDS molecules and its radical ions showed charge transfer not to be the cause for the shortening of the exocyclic C=S bonds.
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[60]富勒烯与2-(4-硫酮-1,3-二硫胺-5-基登)-4,5-二甲基-1,3-二烯醇的分子配合物[C60·2(DTDS)]的合成、晶体结构和性质
摘要合成了[60]富勒烯与2-(4-硫酮- 1,3 -二硫胺-5-基登)-4,5-二甲基- 1,3 -二烯醇[C60·2(DTDS)]的新型分子配合物,并对其晶体结构、红外光谱和电化学性能进行了研究。发现了部分电荷转移。发现DTDS分子内环S-C(sp2)键的异常缩短是由>CH2基团的构象振动引起的。对比分析了[C60·2(DTDS)]晶体的x射线数据和DTDS分子及其自由基离子的量子化学计算(SCF MO, 6-31G*基),表明电荷转移不是导致外环C=S键缩短的原因。
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