首页> 美国卫生研究院文献>Chemical Science >Expansion of the (BB) 〉metallacycle with coinage metal cations: formation ofB–M–Ru–B (M = Cu Ag Au) dimetalacyclodiboryls
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Expansion of the (BB) 〉metallacycle with coinage metal cations: formation ofB–M–Ru–B (M = Cu Ag Au) dimetalacyclodiboryls

机译:(BB)〉金属环与造币金属阳离子的膨胀:B–M–Ru–B(M = CuAgAu)双金属环二硼烷基

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摘要

In this work, we introduce a novel approach for the selective assembly of heterometallic complexes by unprecedented coordination of coinage metal cations to strained single ruthenium–boron bonds on a surface of icosahedral boron clusters. M(i) cations (M = Cu, Ag, and Au) insert into B–Ru bonds of the (BB)–carboryne complex of ruthenium with the formation of four-membered B–M–Ru–B metalacycles. Results of theoretical calculations suggest that bonding within these metalacycles can be best described as unusual three-center-two-electron B–M···Ru interactions that are isolobal to B–H···Ru borane coordination for M = Cu and Ag, or the pairs of two-center-two electron B–Au and Au–Ru interactions for M = Au. These transformations comprise the first synthetic route to exohedral coinage metal boryl complexes of icosahedral closo-{C2B10} clusters, which feature short Cu–B (2.029(2) Å) and Ag–B (2.182(3) Å) bonds and the shortest Au–B bond (2.027(2) Å) reported to date. The reported heterometallic complexes contain Cu(i) and Au(i) centers in uncharacteristic square-planar coordination environments. These findings pave the way to rational construction of a broader class of multimetallic architectures featuring M–B bonds.
机译:在这项工作中,我们介绍了一种新颖的方法,该方法通过将造币金属阳离子与二十面体硼团簇表面上的单个钌-硼键进行空前的配位,从而选择性地组装异金属配合物。 M(i)阳离子(M = Cu,Ag和Au)插入钌(BB)-carboryne配合物的B-Ru键中,并形成四元B-M-Ru-B金属环。理论计算结果表明,这些金属环内的键合可以最好地描述为三中心两电子的B–M···Ru相互作用,与M = Cu和Ag的B–H···Ru硼烷配位等价,或M = Au的两对二电子B–Au和Au–Ru相互作用对。这些转变是向二十面体closo- {C2B10}簇的外面铸币金属硼基络合物的第一个合成路线,其特征在于具有短的Cu–B(2.029(2)Å)和Ag–B(2.182(3)Å)键,且键合最短迄今已报告了Au-B键(2.027(2)Å)。报道的杂金属络合物在非特征性的方形平面配位环境中包含Cu(i)和Au(i)中心。这些发现为合理构造具有M-B键的更广泛的多金属体系结构铺平了道路。

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