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首页> 外文期刊>Crystal growth & design >Structural transformations of Pb(II)- trans -1,2-bis(4′-pyridyl) ethene coordination polymers in solution
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Structural transformations of Pb(II)- trans -1,2-bis(4′-pyridyl) ethene coordination polymers in solution

机译:溶液中Pb(II)-反式-1,2-双(4'-吡啶基)乙烯配位聚合物的结构转变

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摘要

Reaction of bpe (bpe = trans-1,2-bis(4′-pyridyl)ethylene) with Pb(OAc)_2?3H_2O in the presence of trifluoroacetic acid (HTFA) affords a triple-stranded coordination polymer (CP) [Pb _3(μ-bpe)_3(μ-O_2CCF_3) _2(μ-O_2CCH_3)_2(O _2CCF_3)_2] (1) in two days, which undergoes structural transformation in solution to yield a two-dimensional (2D) sheet-like CP [Pb(μ-bpe)(μ-O_2CCH_3)(O_2CCF _3)]?0.25bpe?1.75H_2O (2) in three weeks; finally compound 2 rearranges to [Pb(μ-bpe)(O_2CCH_3)(O _2CCF_3)] (3) in the fourth week. Compound 3 has a molecular fabric-like interwoven structure formed by spiral one-dimensional (1D) coordination polymeric chains. Reaction of bpe with Pb(O_2CCF _3)_2 and Pb(OAc)_2?3H_2O respectively in equimolar ratio produces [Pb(μ-bpe)(μ-O _2CCF_3)_2] (4) and [Pb(μ-bpe)(O _2CCH_3)_2]?0.25H_2O (5). The compound 4 is a three-dimensional (3D) CP with a 4~2.6 ~3.8-sra (SrAl_2) topology, whereas 5 has a double-stranded structure with Pb(II)???π (pyridyl) interactions between 1D chains. The compounds [Pb(μ-bpe)(μ-O_2CCH_3)(O _2CCF_3)]?0.25bpe (2a), 4, and 5 have been characterized by X-ray crystallography, while 1 and 3 were reported before. The factors influencing the rearrangement of CPs in solution have been discussed. The structural topological features observed in 2a, 4, and 5 have been attributed to the coordination preference of the Pb(II) and the carboxylate ligands.
机译:在三氟乙酸(HTFA)存在下,bpe(bpe =反式-1,2-双(4'-吡啶基)乙烯)与Pb(OAc)_2?3H_2O的反应提供了三链配位聚合物(CP)[Pb _3(μ-bpe)_3(μ-O_2CCF_3)_2(μ-O_2CCH_3)_2(O _2CCF_3)_2](1)在两天内进行溶液中的结构转化,以产生二维(2D)片状CP [Pb(μ-bpe)(μ-O_2CCH_3)(O_2CCF _3)]?0.25bpe?1.75H_2O(2)在三周内;最后化合物2在第四周重新排列为[Pb(μ-bpe)(O_2CCH_3)(O _2CCF_3)](3)。化合物3具有由螺旋一维(1D)配位聚合物链形成的分子织物状交织结构。 bpe与等摩尔比分别与Pb(O_2CCF _3)_2和Pb(OAc)_2?3H_2O反应生成[Pb(μ-bpe)(μ-O_2CCF_3)_2](4)和[Pb(μ-bpe)( O _2CCH_3)_2]?0.25H_2O(5)。化合物4是具有4〜2.6〜3.8-sra(SrAl_2)拓扑结构的三维(3D)CP,而化合物5具有一维链之间具有Pb(II)???π(吡啶基)相互作用的双链结构。 。化合物[Pb(μ-bpe)(μ-O_2CCH_3)(O _2CCF_3)]≤0.25bpe(2a),4和5已通过X射线晶体学进行了表征,而之前已报道了1和3。讨论了影响溶液中CP重排的因素。在2a,4和5中观察到的结构拓扑特征归因于Pb(II)和羧酸盐配体的配位偏爱。

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