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含碲的混合硫属元素PNP配体的合成、核磁共振表征及X射线结构:SeiPr2PNP(H)iPr2和[NaN(EPiPr2)2]∞(E = Se,Te)的晶体结构

Synthesis, NMR characterisation and X-ray structures of mixed chalcogenido PNP ligands containing tellurium: crystal structures of SeiPr2PNP(H)iPr2 and [NaN(EPiPr2)2]infinity (E = Se, Te).

作者信息

Robertson Stuart D, Chivers Tristram

机构信息

Department of Chemistry, University of Calgary, 2500 University Drive NW, Calgary, AB T2N 1N4, Canada.

出版信息

Dalton Trans. 2008 Apr 7(13):1765-72. doi: 10.1039/b717287g. Epub 2008 Feb 20.

Abstract

Reaction of HN(PiPr2)2 with one equivalent of selenium in hexane at room temperature yields the monoselenide as the P-H tautomer Se=PiPr2-N=P(H)iPr2 (2b). Deprotonation of 2b with n butyllithium in the presence of TMEDA at -78 degrees C followed by addition of tellurium produces the air-sensitive, mixed chalcogenido complex [(TMEDA)Li(SePiPr2)(TePiPr2)N] (8Li) in >97% purity after recrystallisation. Similarly, deprotonation of Te=PiPr2-N=P(H)iPr2 (2c), followed by addition of sulfur, gives the sulfur analogue [(TMEDA)Li(SPiPr2)(TePiPr2)N] (7Li) in >99% purity. The symmetrical complexes [(TMEDA)Li(SePiPr2)2N] (4Li) and [(TMEDA)Li(TePiPr2)2N] (5Li) are produced by similar methods. Compounds 2b, 4Li, 5Li, 7Li and 8Li were characterised in solution by multinuclear (1H, 31P, 77Se and 125Te) NMR spectroscopy and their solid-state structures were determined by X-ray crystallography. The X-ray crystal structures of the polymeric chains [NaN(EPiPr2)2]infinity (4Na, E = Se and 5Na, E = Te) are also reported.

摘要

HN(PiPr2)2与一当量的硒在室温下于己烷中反应,生成单硒化物,其为P-H互变异构体Se=PiPr2-N=P(H)iPr2 (2b)。在-78℃下,在TMEDA存在下用正丁基锂对2b进行去质子化,然后加入碲,重结晶后得到纯度>97%的对空气敏感的混合硫属化物配合物[(TMEDA)Li(SePiPr2)(TePiPr2)N] (8Li)。类似地,对Te=PiPr2-N=P(H)iPr2 (2c)进行去质子化,然后加入硫,得到纯度>99%的硫类似物[(TMEDA)Li(SPiPr2)(TePiPr2)N] (7Li)。对称配合物[(TMEDA)Li(SePiPr2)2N] (4Li)和[(TMEDA)Li(TePiPr2)2N] (5Li)通过类似方法制备。化合物2b、4Li、5Li、7Li和8Li在溶液中通过多核(1H、31P、77Se和125Te)核磁共振光谱进行表征,并通过X射线晶体学确定其固态结构。还报道了聚合物链[NaN(EPiPr2)2]∞(4Na,E = Se;5Na,E = Te)的X射线晶体结构。

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