6-[4-(tert-Butyl­dimethyl­sil­yloxy)phen­yl]-1-oxa­spiro­[2.5]hepta­ne

IUCrData Pub Date : 2024-06-01 DOI:10.1107/S241431462400590X
Edward A. Wetzel , Sergey Lindeman , William A. Donaldson , W. T. A. Harrison (Editor)
{"title":"6-[4-(tert-Butyl­dimethyl­sil­yloxy)phen­yl]-1-oxa­spiro­[2.5]hepta­ne","authors":"Edward A. Wetzel ,&nbsp;Sergey Lindeman ,&nbsp;William A. Donaldson ,&nbsp;W. T. A. Harrison (Editor)","doi":"10.1107/S241431462400590X","DOIUrl":null,"url":null,"abstract":"<div><p>In the title compound, the O atom of the epoxide group has a pseudoaxial orientation and the dihedral angle between the cyclo­hexyl and benzene rings is 85.80 (8)°. The C—O—Si—C<sub>t</sub> (<em>t</em> = <em>tert</em>-but­yl) torsion angle is −177.40 (14)°. In the crystal, pairwise C—H⋯O links connect the mol­ecules into inversion dimers featuring <figure><img></figure>(8) loops.</p></div><div><p>The title compound, C<sub>19</sub>H<sub>30</sub>O<sub>2</sub>Si, has triclinic (<em>P</em><figure><img></figure>) symmetry at 100 K. The O atom of the epoxide group has a pseudoaxial orientation and the dihedral angle between the cyclo­hexyl and benzene rings is 85.80 (8)°. The C—O—Si—C<sub>t</sub> (<em>t</em> = <em>tert</em>-but­yl) torsion angle is −177.40 (14)°. In the crystal, pairwise C—H⋯O links connect the mol­ecules into inversion dimers featuring <em>R</em><sup>2</sup><sub>2</sub>(8) loops.<span><figure><span><img><ol><li><span>Download : <span>Download high-res image (200KB)</span></span></li><li><span>Download : <span>Download full-size image</span></span></li></ol></span></figure></span></p></div>","PeriodicalId":94324,"journal":{"name":"IUCrData","volume":"9 6","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11223687/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IUCrData","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2414314624000609","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

In the title compound, the O atom of the epoxide group has a pseudoaxial orientation and the dihedral angle between the cyclo­hexyl and benzene rings is 85.80 (8)°. The C—O—Si—Ct (t = tert-but­yl) torsion angle is −177.40 (14)°. In the crystal, pairwise C—H⋯O links connect the mol­ecules into inversion dimers featuring

(8) loops.

The title compound, C19H30O2Si, has triclinic (P

) symmetry at 100 K. The O atom of the epoxide group has a pseudoaxial orientation and the dihedral angle between the cyclo­hexyl and benzene rings is 85.80 (8)°. The C—O—Si—Ct (t = tert-but­yl) torsion angle is −177.40 (14)°. In the crystal, pairwise C—H⋯O links connect the mol­ecules into inversion dimers featuring R22(8) loops.
  1. Download : Download high-res image (200KB)
  2. Download : Download full-size image

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
6-[4-(tert-Butyl-dimethyl-sil-yloxy)phen-yl]-1-oxa-spiro-[2.5]hepta-ne.
标题化合物 C19H30O2Si 在 100 K 时具有三菱(P)对称性。环氧基团的 O 原子具有假轴向,环己基和苯环之间的二面角为 85.80 (8)°。C-O-Si-C t(t = 叔丁基)扭转角为-177.40 (14)°。在晶体中,成对的 C-H⋯O 链接将分子结构连接成具有 R 2 2(8)环的反转二聚体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
0.30
自引率
0.00%
发文量
0
期刊最新文献
3-(2-Hy-droxy-eth-yl)-1-(4-nitro-phen-yl)-1H-imidazol-3-ium bromide. 4'-(2-Meth-oxy-phen-yl)-2,2':6',2''-terpyridine. 3,5,6-Tri-chloro-pyridin-2-ol. 4-Amino-3,5-di-chloro-pyridine. Bis(azido-κN 1)bis-(2,2'-di-pyridyl-amine-κ2 N 1,N 1')iron(II) monohydrate.
×
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