N. Spitsina, S. V. Konovalikhin, A. Lobach, E. Golubev, M. Kaplunov, O. A. D’yachenko
{"title":"[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","authors":"N. Spitsina, S. V. Konovalikhin, A. Lobach, E. Golubev, M. Kaplunov, O. A. D’yachenko","doi":"10.1080/10641220009351434","DOIUrl":null,"url":null,"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.","PeriodicalId":12470,"journal":{"name":"Fullerene Science and Technology","volume":"13 1","pages":"561 - 576"},"PeriodicalIF":0.0000,"publicationDate":"2000-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"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\",\"authors\":\"N. Spitsina, S. V. Konovalikhin, A. Lobach, E. Golubev, M. Kaplunov, O. A. D’yachenko\",\"doi\":\"10.1080/10641220009351434\",\"DOIUrl\":null,\"url\":null,\"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.\",\"PeriodicalId\":12470,\"journal\":{\"name\":\"Fullerene Science and Technology\",\"volume\":\"13 1\",\"pages\":\"561 - 576\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Fullerene Science and Technology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/10641220009351434\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fullerene Science and Technology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10641220009351434","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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
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.