{"title":"反十二烷基异丙基三环-[4.2.00.0(2,5)]辛烷的手性结晶。","authors":"R. Tanaka, S. Kyushin, M. Unno, H. Matsumoto","doi":"10.1080/10242430212882","DOIUrl":null,"url":null,"abstract":"The aim of this article is to describe the results of our investigation on the chiral crystallization of anti-tricyclic ladder polysilane, anti-dodecaisopropyltricyclo [4.2.0.0(2,5)] octasilane (1). In solid state, the silicon framework of 1 adopts twisted conformation in which the Si4 rings are puckered in the same direction. Crystallization of 1 afforded a large conglomerate crystal in high yield. X-ray crystallography revealed that the crystal consists of either right-handed (P) or left-handed (M) molecules. The ultraviolet and circular dichroism spectra of the chiral crystals of 1 reveal two absorption bands in the 400-250 nm region.","PeriodicalId":11752,"journal":{"name":"Enantiomer","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2002-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Chiral crystallization of anti-dodecaisopropyltricyclo-[4.2.00.0(2,5)] octasilane.\",\"authors\":\"R. Tanaka, S. Kyushin, M. Unno, H. Matsumoto\",\"doi\":\"10.1080/10242430212882\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The aim of this article is to describe the results of our investigation on the chiral crystallization of anti-tricyclic ladder polysilane, anti-dodecaisopropyltricyclo [4.2.0.0(2,5)] octasilane (1). In solid state, the silicon framework of 1 adopts twisted conformation in which the Si4 rings are puckered in the same direction. Crystallization of 1 afforded a large conglomerate crystal in high yield. X-ray crystallography revealed that the crystal consists of either right-handed (P) or left-handed (M) molecules. The ultraviolet and circular dichroism spectra of the chiral crystals of 1 reveal two absorption bands in the 400-250 nm region.\",\"PeriodicalId\":11752,\"journal\":{\"name\":\"Enantiomer\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Enantiomer\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/10242430212882\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Enantiomer","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/10242430212882","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Chiral crystallization of anti-dodecaisopropyltricyclo-[4.2.00.0(2,5)] octasilane.
The aim of this article is to describe the results of our investigation on the chiral crystallization of anti-tricyclic ladder polysilane, anti-dodecaisopropyltricyclo [4.2.0.0(2,5)] octasilane (1). In solid state, the silicon framework of 1 adopts twisted conformation in which the Si4 rings are puckered in the same direction. Crystallization of 1 afforded a large conglomerate crystal in high yield. X-ray crystallography revealed that the crystal consists of either right-handed (P) or left-handed (M) molecules. The ultraviolet and circular dichroism spectra of the chiral crystals of 1 reveal two absorption bands in the 400-250 nm region.
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