Synthesis and Structural Characterization of Base-Stabilized Oligomeric Heterovinylidenes
收藏NIAID Data Ecosystem2026-03-07 收录
下载链接：
https://figshare.com/articles/dataset/Synthesis_and_Structural_Characterization_of_Base_Stabilized_Oligomeric_Heterovinylidenes/2385559
下载链接
链接失效反馈官方服务：
资源简介：
Metalation of the (iminophosphoranyl)phosphine
PPh2CH2(PPh2NSiMe3) (1) with an equimolar amount of n-BuLi afforded the monolithium salt [Li{CH(PPh2)(PPh2NSiMe3)}(THF)2] (2). The reaction of 2 with GeCl2·1,4-dioxane
has led to the formation of a germavinylene moiety, which trimerized
to form a new heterocyclic cage compound, [{(PPh2NSiMe3)(PPh2)CGe:}{(PPh2NSiMe3)(PPh2)C}2Ge→Ge:] (3). A similar reaction of the lithium methanide complex 2 with SnCl2 afforded the stannavinylidene moiety, which
underwent a “head-to-tail” cycloaddition to form a stable
1,3-distannacyclobutane, 4. A trapping reaction of 4 with diiron nonacarbonyl gave the novel iron stannavinylidene
complex 5. The solid-state structure analysis of 5 reveals that it contains two stannavinylidene moieties bonded
in a Sn–P “head-to-tail” fashion, with one of
the tin(II) centers coordinating to a Fe(CO)4 moiety. The
X-ray structures of 2–5 have been
determined by X-ray crystallography. In addition, the dynamic behavior
of 5 has been studied by means of variable-temperature 31P and 119Sn NMR spectroscopy.
创建时间：
2013-08-19
