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Metal coordination of phosphoniocarbynes.
Dalton Transactions ( IF 3.5 ) Pub Date : 2020-08-24 , DOI: 10.1039/d0dt02737e
Chee S Onn 1 , Anthony F Hill 1 , Angus Olding 1
Affiliation  

Heterobi- and tetrametallic phosphoniocarbyne bridged complexes [WAu(μ-CPMe2Ph)Cl(CO)2(Tp*)]+ (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate), [W2Cu2(μ-CPMe2Ph)2(μ-Cl)2(CO)4(Tp*)2]2+ and [WPt(μ-CPMe2Ph)(COD)(CO)2(Tp*)]+ (COD = 1,5-cyclo-octadiene) arise from the reactions of the mononuclear terminal phosphoniocarbyne [W([triple bond, length as m-dash]CPMe2Ph)(CO)2(Tp*)]PF6 with [AuCl(THT)] (THT = tetrahydrothiophene), [CuCl(SMe2)] and [Pt(nbe)3] (nbe = norbornene) in the presence of COD. The COD ligand in [WPt(μ-CPMe2Ph)(COD)(CO)2(Tp*)]+ is labile and readily replaced by isonitriles to provide [WPt(μ-CPMe2Ph)(CNR)2(CO)2(Tp*)]+ (R = tBu, C6H2Me3-2,4,6) with retention of the tungstaplatinacyclopropene core, the bonding within which was computationally interrogated.

中文翻译:

膦碳碳炔的金属配位。

Heterobi-和tetrametallic phosphoniocarbyne桥连络合物[WAU(μ-CPME 2 PH)氯(CO)2(TP *)] +(TP * =氢三(3,5-二甲基吡唑-1-基)硼酸盐),[W 22(μ-CPME 2 PH)2(μ-Cl)的2(CO)4(TP *)2 ] 2+和[WPT(μ-CPME 2 PH)(COD)(CO)2(TP *)] +(COD = 1,5-环辛二烯)源自单核末端膦碳碳[三重键,长度为m-破折号]炔[W(CPMe 2 Ph)(CO)2(Tp *)] PF 6的反应在COD存在下,用[AuCl(THT)](THT =四氢噻吩),[CuCl(SMe 2)]和[Pt(nbe)3 ](nbe =降冰片烯)。COD的配体[WPT(μ-CPME 2 PH)(COD)(CO)2(TP *)] +是不稳定的和容易地通过异腈代替,以提供[WPT(μ-CPME 2 PH)(CNR)2(CO )2(Tp *)] +(R = t Bu,C 6 H 2 Me 3 -2,4,6),同时保留钨铂环戊丙烯核心,其中的键在计算上受到询问。
更新日期:2020-09-22
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