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一种新型富马酸镧(III)配位聚合物的水热合成与晶体结构

Hydro-thermal synthesis and crystal structure of a new lanthanum(III) coordination polymer with fumaric acid.

作者信息

Anana Hayet, Trifa Chahrazed, Bouacida Sofiane, Boudaren Chaouki, Merazig Hocine

机构信息

Unité de Recherche de Chimie de l'Environnement et Moléculaire Structurale, CHEMS, Université Constantine 1, 25000 , Algeria.

Département Sciences de la Matière, Faculté des Sciences Exactes et Sciences de la Nature et de la Vie, Université Larbi Ben M'hidi, Oum El Bouaghi, Algeria ; Unité de Recherche de Chimie de l'Environnement et Moléculaire Structurale, CHEMS, Université Constantine 1, 25000 , Algeria.

出版信息

Acta Crystallogr E Crystallogr Commun. 2015 Apr 22;71(Pt 5):m114-5. doi: 10.1107/S2056989015007008. eCollection 2015 May 1.

DOI:10.1107/S2056989015007008
PMID:25995891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4420125/
Abstract

The title compound, poly[di-aqua-tris-(μ4-but-2-enedioato)(μ2-but-2-enedioic acid)dilanthanum(III)], [La2(C4H2O4)3(C4H4O4)(H2O)2] n , was synthesized by the reaction of lanthanum chloride penta-hydrate with fumaric acid under hydro-thermal conditions. The asymmetric unit comprises an La(III) cation, one and a half fumarate dianions (L (2-)), one a half-mol-ecule of fumaric acid (H2 L) and one coordinated water mol-ecule. Each La(III) cation has the same nine-coordinate environment and is surrounded by eight O atoms from seven distinct fumarate moieties, including one proton-ated fumarate unit and one water mol-ecule in a distorted tricapped trigonal-prismatic environment. The LaO8(H2O) polyhedra centres are edge-shared through three carboxyl-ate bridges of the fumarate ligand, forming chains in three dimensions to construct the MOF. The crystal structure is stabilized by O-H⋯O hydrogen-bond inter-actions between the coordin-ated water mol-ecule and the carboxyl-ate O atoms, and also between oxygen atoms of fumaric acid.

摘要

标题化合物聚[二水合-三-(μ4-丁-2-烯二酸根)(μ2-丁-2-烯二酸)二镧(III)],[La₂(C₄H₂O₄)₃(C₄H₄O₄)(H₂O)₂]ₙ,是通过水合氯化镧与富马酸在水热条件下反应合成的。不对称单元包括一个La(III)阳离子、一个半富马酸二价阴离子(L²⁻)、一个半富马酸分子(H₂L)和一个配位水分子。每个La(III)阳离子具有相同的九配位环境,被来自七个不同富马酸部分的八个O原子包围,包括一个质子化的富马酸单元和一个水分子,处于扭曲的三帽三棱柱环境中。LaO₈(H₂O)多面体中心通过富马酸配体的三个羧酸根桥边共享,在三维空间中形成链以构建金属有机框架。晶体结构通过配位水分子与羧酸根O原子之间以及富马酸的氧原子之间的O—H⋯O氢键相互作用得以稳定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bccc/4420125/026cc846fa17/e-71-0m114-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bccc/4420125/0087b342ff9a/e-71-0m114-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bccc/4420125/638d0f2ac4fe/e-71-0m114-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bccc/4420125/026cc846fa17/e-71-0m114-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bccc/4420125/0087b342ff9a/e-71-0m114-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bccc/4420125/638d0f2ac4fe/e-71-0m114-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bccc/4420125/026cc846fa17/e-71-0m114-fig3.jpg

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本文引用的文献

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Synthesis and Biological Activity of Manganese (II) Complexes of Phthalic and Isophthalic Acid: X-Ray Crystal Structures of [Mn(ph)(Phen)(2)(H(2)O)]. 4H(2)O, [Mn(Phen)(2)(H(2)O)(2)](2)(Isoph)(2)(Phen). 12H(2)O and {[Mn(Isoph)(bipy)](4). 2.75biby}(n)(phH(2) = Phthalic Acid; isoph = Isophthalic Acid; phen = 1,10-Phenanthroline; bipy = 2,2-Bipyridine).邻苯二甲酸和间苯二甲酸锰(II)配合物的合成及生物活性:[Mn(ph)(Phen)(2)(H(2)O)]. 4H(2)O、[Mn(Phen)(2)(H(2)O)(2)](2)(Isoph)(2)(Phen). 12H(2)O和{[Mn(Isoph)(bipy)](4). 2.75biby}(n)的X射线晶体结构(phH(2)=邻苯二甲酸;isoph=间苯二甲酸;phen=1,10-菲咯啉;bipy=2,2-联吡啶)
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