tert-Butyldichlorophosphane: crystal structure and its reactivity towards supersilyl sodium

L. Fink, Marcel Bamberg, E. Alig, H. Lerner
{"title":"tert-Butyldichlorophosphane: crystal structure and its reactivity towards supersilyl sodium","authors":"L. Fink, Marcel Bamberg, E. Alig, H. Lerner","doi":"10.1515/znb-2023-0041","DOIUrl":null,"url":null,"abstract":"Abstract Crystals of tBuPCl2 were obtained by a short-path sublimation at 80 °C/0.150 mbar. The structure determination of tBuPCl2 was based on X-ray powder data. The measurements were carried out in a temperature range from 173 K to r. t. At 173 K the X-ray powder pattern has been assigned to an orthorhombic phase, and that at 213 K to a plastic-crystalline, cubic phase. We further investigated the reactivity of tBuPCl2 towards Na(thf)2[SitBu3] at ambient temperature. The reaction of tBuPCl2 with two equivalents of Na(thf)2[SitBu3] gave together with tBu3SiCl the yet unknown phosphanediide Na2[PtBu] by a chlorine-sodium exchange. The identity of Na2[PtBu] was confirmed by 31P NMR spectroscopy and its existence was unambiguously demonstrated by its protonation with methanol and the consequent formation of tBuPH2.","PeriodicalId":23831,"journal":{"name":"Zeitschrift für Naturforschung B","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-09-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Zeitschrift für Naturforschung B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1515/znb-2023-0041","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

Abstract Crystals of tBuPCl2 were obtained by a short-path sublimation at 80 °C/0.150 mbar. The structure determination of tBuPCl2 was based on X-ray powder data. The measurements were carried out in a temperature range from 173 K to r. t. At 173 K the X-ray powder pattern has been assigned to an orthorhombic phase, and that at 213 K to a plastic-crystalline, cubic phase. We further investigated the reactivity of tBuPCl2 towards Na(thf)2[SitBu3] at ambient temperature. The reaction of tBuPCl2 with two equivalents of Na(thf)2[SitBu3] gave together with tBu3SiCl the yet unknown phosphanediide Na2[PtBu] by a chlorine-sodium exchange. The identity of Na2[PtBu] was confirmed by 31P NMR spectroscopy and its existence was unambiguously demonstrated by its protonation with methanol and the consequent formation of tBuPH2.
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
叔丁基二氯膦:晶体结构及其对超硅基钠的反应性
在80 °C/0.150 mbar下,通过短程升华获得了tBuPCl2晶体。基于x射线粉末数据确定了tBuPCl2的结构。测量是在173 K到rt的温度范围内进行的。在173 K时,x射线粉末模式被指定为正交相,而在213 K时,x射线粉末模式被指定为塑性结晶,立方相。我们进一步研究了tBuPCl2在室温下对Na(thf)2[SitBu3]的反应性。bupcl2与两种等效的Na(thf)2[SitBu3]反应,通过氯-钠交换,与tBu3SiCl一起生成未知的磷二化物Na2[PtBu]。Na2[PtBu]的身份被31P核磁共振光谱证实,它的存在被明确地证明了它与甲醇的质子化和随后形成的tBuPH2。
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
自引率
0.00%
发文量
0
期刊最新文献
Brass corrosion – dezincification in hydrochloric acid A base-promoted synthesis of 3,4-dihydro-2(1H)-quinazolinones Comprehensive structural evaluation of the quaternary chalcogenide Ag2CdSnSe4 Refrachor (F) – seventy-year-old tool and a contemporary observation: estimation of equilibrium compositions of 1H- and 2H-tautomers of tetrazole and 1,2,3-triazole and imine–amine composition of acetaldimine–vinylamine tautomerism Selectfluor-triggered C–H halogenations of enaminones with copper(I) halide (CuX) for the synthesis of 3-halochromones
×
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