2,5-二苯基-1,4-二硫胺1-氧化物的晶体、分子和电子结构

G. Bandoli, C. Panattoni, D. A. Clemente, E. Tondello, A. Dondoni, A. Mangini
{"title":"2,5-二苯基-1,4-二硫胺1-氧化物的晶体、分子和电子结构","authors":"G. Bandoli, C. Panattoni, D. A. Clemente, E. Tondello, A. Dondoni, A. Mangini","doi":"10.1039/J29710001407","DOIUrl":null,"url":null,"abstract":"The crystal structure of 2,5-diphenyl-1,4-dithiin 1-oxide, C16H12O2S2, has been determined by a three-dimensional X-ray analysis. The crystals are orthorhombic, space group Pbca, with cell dimensions of a= 27·855, b= 12·162, and c= 8·089 A and Z= 8. The structure has been solved, by the symbolic-addition procedure, from 702 reflections collected by counter, and refined by least-squares methods to R 0·05.The heterocyclic ring is arranged in a boat structure with the sulphinyl oxygen in the axial position; the phenyl rings lie below the plane of the two CC bonds. The arrangement around the oxidized sulphur is slightly distorted pyramidal with the sulphur atom at the apex. The C–S bonds have different lengths: the two bonds to the unoxidized sulphur are significantly shorter than the C–S distance for the other two bonds to the sulphoxidic sulphur. This situation is discussed in terms of the CNDO method.","PeriodicalId":17268,"journal":{"name":"Journal of The Chemical Society B: Physical Organic","volume":"86 1","pages":"1407-1411"},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Crystal, molecular, and electronic structure of 2,5-diphenyl-1,4-dithiin 1-oxide\",\"authors\":\"G. Bandoli, C. Panattoni, D. A. Clemente, E. Tondello, A. Dondoni, A. Mangini\",\"doi\":\"10.1039/J29710001407\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The crystal structure of 2,5-diphenyl-1,4-dithiin 1-oxide, C16H12O2S2, has been determined by a three-dimensional X-ray analysis. The crystals are orthorhombic, space group Pbca, with cell dimensions of a= 27·855, b= 12·162, and c= 8·089 A and Z= 8. The structure has been solved, by the symbolic-addition procedure, from 702 reflections collected by counter, and refined by least-squares methods to R 0·05.The heterocyclic ring is arranged in a boat structure with the sulphinyl oxygen in the axial position; the phenyl rings lie below the plane of the two CC bonds. The arrangement around the oxidized sulphur is slightly distorted pyramidal with the sulphur atom at the apex. The C–S bonds have different lengths: the two bonds to the unoxidized sulphur are significantly shorter than the C–S distance for the other two bonds to the sulphoxidic sulphur. This situation is discussed in terms of the CNDO method.\",\"PeriodicalId\":17268,\"journal\":{\"name\":\"Journal of The Chemical Society B: Physical Organic\",\"volume\":\"86 1\",\"pages\":\"1407-1411\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society B: Physical Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J29710001407\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society B: Physical Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J29710001407","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

用三维x射线分析确定了2,5-二苯基-1,4-二硫胺1-氧化物C16H12O2S2的晶体结构。晶体为正交晶格,空间群为Pbca,胞元尺寸为a= 27.855, b= 12.162, c= 8.089 a, Z= 8。该结构由计数器收集的702个反射信号用符号加法法求解,并用最小二乘法将其细化为r0·05。所述杂环呈船状排列,亚砜基氧在轴向位置;苯环位于两个CC键的平面之下。氧化硫周围的排列呈轻微扭曲的金字塔状,硫原子位于顶端。C-S键有不同的长度:两个键到未氧化硫的C-S距离明显短于其他两个键到亚氧硫的C-S距离。用CNDO方法对这种情况进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Crystal, molecular, and electronic structure of 2,5-diphenyl-1,4-dithiin 1-oxide
The crystal structure of 2,5-diphenyl-1,4-dithiin 1-oxide, C16H12O2S2, has been determined by a three-dimensional X-ray analysis. The crystals are orthorhombic, space group Pbca, with cell dimensions of a= 27·855, b= 12·162, and c= 8·089 A and Z= 8. The structure has been solved, by the symbolic-addition procedure, from 702 reflections collected by counter, and refined by least-squares methods to R 0·05.The heterocyclic ring is arranged in a boat structure with the sulphinyl oxygen in the axial position; the phenyl rings lie below the plane of the two CC bonds. The arrangement around the oxidized sulphur is slightly distorted pyramidal with the sulphur atom at the apex. The C–S bonds have different lengths: the two bonds to the unoxidized sulphur are significantly shorter than the C–S distance for the other two bonds to the sulphoxidic sulphur. This situation is discussed in terms of the CNDO method.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Kinetics and mechanism of electrophilic substitution of heteroaromatic compounds. Part XXIII. Acid-catalysed hydrogen exchange of quinoline, isoquinoline, and their N-oxides Dielectric relaxation and dipole moments of substituted pyrroles Free-radical addition to olefins. Part VII. Addition of trichloromethyl radicals to chloro-olefins Primary hydrogen isotope effects on the rate of ionization of nitroethane in mixtures of water and dimethyl sulphoxide The conformational analysis of saturated heterocycles. Part XXXV. 1-Phenoxymethyl-3,4-dihydroisoquinolines
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1