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Mn(II) coordination architectures with mixed ligands of 3-(2-pyridyl)pyrazole and carboxylic acids bearing different secondary coordination donors and pendant skeletons

机译:具有3-(2-吡啶基)吡唑和羧酸混合配体的Mn(II)配位结构,带有不同的二级配位给体和侧链骨架

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In our efforts to investigate the factors that affect the formation of coordination architectures, such as secondary coordination donors and pendant skeletons of the carboxylic acid ligands, as well as H-bonding and other weak interactions, two kinds of ligands: (a) 3-(2-pyridyl)pyrazole (L-1) with a non-coordinated N atom as a H-bonding donor, a 2,2'-bipyridyl-like chelating ligand, and (b) four carboxylic ligands with different secondary coordination donors and/or pendant skeletons, 1,4-benzenedicarboxylic acid (H2L2), 4-sulfobenzoic acid (H2L3), quinoline-4-carboxylic acid (HL4) and fumaric acid (H2L5), have been selected to react with Mn(II) salts, and five new complexes, [Mn(L-1)(2)(SO4)](2) (1), [Mn(L-1)(2)(L-2)]infinity (2), [Mn(L-1)(HL3)(2)]infinity (3), Mn(L-1)(2)(L-4)(2) (4), and [Mn(L-1)(2)(L-5)]infinity (5), have been obtained and structurally characterized. The structural differences of 1-5 can be attributed to the introduction of the different carboxylic acid ligands (H2L2, H2L3, HL4, and H2L5) with different secondary coordination donors and pendant skeletons, respectively. This result also reveals that the typical H-bonding (i.e. N-H center dot center dot center dot O and O-H center dot center dot center dot O) and some other intra- or inter-molecular weak interactions, such as C-H center dot center dot center dot O weak H-bonding and pi...pi interactions, often play important roles in the formation of supramolecular aggregates, especially in the aspect of linking the multi-nuclear discrete subunits or low-dimensional entities into high-dimensional supramolecular networks. (C) 2007 Elsevier B.V. All rights reserved.
机译:在我们研究影响配位体系形成的因素的努力中,例如羧酸配体的二级配位给体和侧链骨架,以及氢键和其他弱相互作用,两种配体:(a)3- (2-吡啶基)吡唑(L-1),具有非配位的N原子作为H键供体,2,2'-联吡啶基样螯合配体,以及(b)四个具有不同仲配位给体的羧基配体和/或选择侧链骨架,1,4-苯二甲酸(H2L2),4-磺基苯甲酸(H2L3),喹啉-4-羧酸(HL4)和富马酸(H2L5)与Mn(II)盐反应,以及五个新的配合物[Mn(L-1)(2)(SO4)](2)(1),[Mn(L-1)(2)(L-2)]无穷大(2),[Mn (L-1)(HL3)(2)]无穷大(3),Mn(L-1)(2)(L-4)(2)(4)和[Mn(L-1)(2)( L-5)]无穷大(5),已经获得并在结构上表征。 1-5的结构差异可归因于分别引入了具有不同二级配位给体和侧链骨架的不同羧酸配体(H2L2,H2L3,HL4和H2L5)。该结果还揭示了典型的H键(即NH中心点中心点中心点O和OH中心点中心点中心点O)以及其他一些分子内或分子间弱相互作用,例如CH中心点中心点中心点O弱H键和pi ... pi相互作用通常在超分子聚集体的形成中发挥重要作用,尤其是在将多核离散亚基或低维实体连接到高维超分子网络方面。 (C)2007 Elsevier B.V.保留所有权利。

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