Synthesis and study of the stability of phosphane palladacycles

P. Munín, Francisco Reigosa, F. Lucio, Pablo Romarís, J. M. Ortigueira, J. M. Vila, M. Pereira
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引用次数: 0

Abstract

: The chemistry of phosphane palladacycles[1] has been amply developed in last years. This kind of chemistry results interesting due to their applications in numerous fields such as organic synthesis[2], catalysis[3] or as potential biologically active materials[4]. Palladacycles bearing the diphosphine dppm have been described before[5] and we now report a new behavior shown by palladacycles of the type [Pd 2 (Ph 2 PCH 2 PPh 2 −P,P) 2 (C,N:C,N)]. In this case the coordination of dppm spontaneously shifts from chelate to bridging mode in solution giving a core A-frame conformation with two palladium atoms with a chlorido or bromido ligand between them.
磷酰二环的合成及稳定性研究
近年来,磷烷类环类化合物[1]的化学研究得到了充分的发展。这种化学结果很有趣,因为它们在许多领域得到了应用,如有机合成[2]、催化[3]或作为潜在的生物活性材料[4]。承载二膦dppm的钯环以前已经被描述过[5],现在我们报道了一种新的钯环行为[Pd 2 (Ph 2 PCH 2 PPh 2−P,P) 2 (C,N:C,N)]。在这种情况下,dppm的配位在溶液中自发地从螯合模式转变为桥接模式,形成两个钯原子与它们之间的氯或溴配体的核心a -框架构象。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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