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首页> 外文期刊>Dalton transactions: An international journal of inorganic chemistry >Hierarchical self-assembly of heteronuclear co-ordination networks
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Hierarchical self-assembly of heteronuclear co-ordination networks

机译:异核配位网络的分层自组装

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摘要

Two ligands L-1 and L-2 have been prepared which contain a chelating pyrazolyl-pyrDEine group with a pendant aromatic nitrile ( in L-1, a benzonitrile; in L-2, a naphthonitrile). These ligands react with Ag(I) salts to give a range of in.nite coordination networks or dimeric 'boxes' in which the pyrazolyl-pyrDEine chelates and the aromatic nitrile groups both participate in coordination to Ag( I) ions. In contrast, L-1 and L-2 form simple mononuclear tris-chelates [ML3](2+) with. first-row transition metal dications ( M = Co, Ni, Zn) in which the aromatic nitrile groups are pendant such that the complexes can be used as 'complex ligands'. The crystal structures of [M(L-2)(3)](BF4)(2) are based on solely the mer tris-chelate geometry although in solution H-1 NMR spectroscopy reveals a mixture of both fac and mer isomers of the tris-chelates. Reaction of these with Ag( I) ions allows the interaction of the pendant nitrile groups with Ag( I) ions to generate coordination networks based on [ML3](2+) cations being crosslinked by Ag( I) ions. In these networks the [ML3](2+) cations have solely the fac geometry and lie on threefold rotation axes with all three pendant nitrile groups coordinated to Ag( I) ions which are three-coordinate. {[AgM(L-2)(3)][BF4](3)}(infinity) (M = Co, Ni) consist of two interpenetrated ( 10,3) a nets which have opposite chirality at the [M(L-2)(3)](2+) centres but are not strictly enantiomorphic as the two nets are not crystallographically equivalent. {[AgNi(L-1)(3)](BF4)(3)}(infinity) in contrast contains two-dimensional sheets which have a ( 6,3) net structure of hexagonal rings of alternative Ni(II) and Ag( I) centres; although not interpenetrating, two such adjacent ( and enantiomorphic) sheets interact with each other via numerous CH center dot center dot center dot pi interactions between aromatic ligands. Formation of these structures shows that the differential reactivity of the two binding sites in L-1 and L-2 (pyrazolyl-pyrDEine, and nitrile) can be used to generate mixed-metal coordination networks in a hierarchical, stepwise manner.
机译:已经制备了两个配体L-1和L-2,它们含有带有侧基芳族腈的螯合的吡唑基-pyrDEine基团(在L-1中为苄腈;在L-2中为萘腈)。这些配体与Ag(I)盐反应生成一系列in.nite配位网络或二聚体“ box”,其中吡唑基-pyrDEine螯合物和芳族腈基均参与与Ag(I)离子的配位。相反,L-1和L-2与它们形成简单的单核三螯合物[ML3](2+)。第一行过渡金属指示剂(M = Co,Ni,Zn),其中芳族腈基是侧基,因此该络合物可用作“络合物配体”。 [M(L-2)(3)](BF4)(2)的晶体结构仅基于三螯合物的几何形状,尽管在溶液中H-1 NMR光谱揭示了fac和mer异构体的混合物Tris-螯合物。这些与Ag(I)离子的反应允许悬垂的腈基与Ag(I)离子发生相互作用,从而基于[ML3](2+)阳离子被Ag(I)离子交联生成配位网络。在这些网络中,[ML3](2+)阳离子仅具有fac几何形状,并且位于三重旋转轴上,所有三个侧基腈基均与三坐标的Ag(I)离子配位。 {[AgM(L-2)(3)] [BF4](3)}(无穷大)(M = Co,Ni)由两个互穿的(10,3)网组成,这些网在[M(L -2)(3)](2+)中心,但不是严格对映的,因为这两个网在晶体学上不是等效的。 {[AgNi(L-1)(3)](BF4)(3)}(无穷大)包含二维薄片,该薄片具有交替的Ni(II)和Ag六角环的(6,3)净结构(I)中心;尽管不是互穿的,但是两个这样的相邻(和对映体)片通过芳族配体之间的大量CH中心点中心点中心点pi相互作用而彼此相互作用。这些结构的形成表明,L-1和L-2中的两个结合位点(吡唑基-pyrDEine和腈)的反应性不同,可用于以分级,逐步的方式生成混合金属配位网络。

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