Hydrothermal Synthesis, Crystal Structure, and Properties of Nickel(II) Coordination Polymer with 2,2′‐Bipyridyl‐3,3′‐dicarboxylate

Benlai Wu, Hong‐quan Zhang, Hong‐yun Zhang, Qing-An Wu, H. Hou, Yu Zhu, Xiang‐yu Wang
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引用次数: 8

Abstract

Abstract The polymeric complex [Ni(bpdc)(H2O)2] n (bpdc, 2,2′‐bipyridyl‐3,3′‐dicarboxylate dianion) which consist of [Ni(bpdc)(H2O)2] units was synthesized using a hydrothermal method. Its crystal structure was determined by x‐ray crystal diffraction as 1‐D chain‐like polymer. In [Ni(bpdc)(H2O)2] n , each bpdc bridges a Ni(II) pair in a unique tetradentate fashion through its two pyridine nitrogen atoms and two oxygen atoms of two carboxyl groups. Each Ni(II) cation has a slightly distorted octahedral coordination environment where the equatorial plane includes the two nitrogen atoms of one bpdc ligand and two oxygen atoms of another bpdc anion, while the axial positions are occupied by two oxygen atoms of two coordinated water molecules. In the polymeric complex the complicated hydrogen‐bonding network and π–π stacking interaction play an important role for its thermostability.
2,2′-联吡啶基- 3,3′-二羧酸盐镍(II)配位聚合物的水热合成、晶体结构和性能
摘要采用水热法合成了由[Ni(bpdc)(H2O)2]单元组成的聚合物配合物[Ni(bpdc)(H2O)2] n (bpdc, 2,2′‐联吡啶基‐3,3′‐二羧酸二碘离子)。通过x射线晶体衍射测定其晶体结构为1 - D类链状聚合物。在[Ni(bpdc)(H2O)2] n中,每个bpdc通过其两个吡啶氮原子和两个羧基的两个氧原子以独特的四齿方式桥接Ni(II)对。每个Ni(II)阳离子具有轻微扭曲的八面体配位环境,其中赤道面包括一个bpdc配体的两个氮原子和另一个bpdc阴离子的两个氧原子,而轴向位置由两个配位水分子的两个氧原子占据。在聚合物配合物中,复杂的氢键网络和π -π堆积相互作用对其热稳定性起着重要作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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