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Kinetic stabilisation of a molecular strontium hydride complex using an extremely bulky amidinate ligand
Chemical Communications ( IF 4.3 ) Pub Date : 2018-01-02 00:00:00 , DOI: 10.1039/c7cc09362d
Caspar N. de Bruin-Dickason 1, 2, 3 , Thomas Sutcliffe 1, 2, 3 , Carlos Alvarez Lamsfus 4, 5, 6 , Glen B. Deacon 1, 2, 3 , Laurent Maron 4, 5, 6 , Cameron Jones 1, 2, 3
Affiliation  

Two extremely bulky amidinate ligands, [RC{N(Dip)}{N(Ar)}] (Dip = 2,6-diisopropylphenyl; Ar = C6H2{C(H)Ph2}2Pri-2,6,4; R = 1-adamantyl (LAd), tert-butyl (LtBu)) have been developed and utilised for the kinetic stabilisation of the strontium and magnesium hydride complexes, [LAdSr(μ-H)]2 and [LRMg(μ-H)]2 (R = Ad or But). The former represents the missing link in the series of dimeric systems, [LAe(μ-H)]2 (Ae = alkaline earth metal). The structure and bonding of the complexes have been studied by crystallographic, spectroscopic and computational techniques.

中文翻译:

使用极其庞大的a酰胺配体对分子氢化锶配合物进行动力学稳定化

两个非常庞大的a基配体[RC {N(Dip)} {N(Ar )}] -(Dip = 2,6-二异丙基苯基; Ar = C 6 H 2 {C(H)Ph 2 } 2 Pr i -2,6,4; R = 1-金刚烷基(L Ad),丁基(L t Bu))已开发并用于锶和氢化镁配合物的动力学稳定,[L Ad Sr(μ- H)] 2和[L R Mg(μ-H)] 2(R = Ad或Bu t)。前者表示二聚体系统[LAe(μ-H)]系列中的缺失环节2(Ae =碱土金属)。已经通过晶体学,光谱学和计算技术研究了配合物的结构和键合。
更新日期:2018-01-18
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