以草酸及咪唑基配体构筑的二维网状锌(Ⅱ)配位聚合物的合成、晶体结构及荧光性质(英文)
Synthesis, Crystal Structure and Fluorescent Property of a 2D Network Zn(Ⅱ) Coordination Polymer Based on Oxalic Acid and Bis(imidazol) Ligand
作者单位
战佩英 通化师范学院化学系通化 134002 
纪建业 通化师范学院化学系通化 134002 
牛艳玲 通化师范学院化学系通化 134002 
王志涛 通化师范学院化学系通化 134002 
李秀梅 通化师范学院化学系通化 134002 
摘要: 通过水热法合成了一个新的配位聚合物[Zn(C2O4)(1,3-bix)]n (1,H2C2O4 =草酸,1,3-bix=1,3-双(咪唑基-1-甲基)-苯)。并对其进行了元素分析、红外光谱、热重和X-射线单晶衍射测定。该配合物属于三斜晶系,P1 空间群。在晶体结构中,锌原子为六配位与来自2个不同的C2O42-配体上的4个羧基氧原子和来自2个不同的1,3-bix配体上的2个氮原子配位,呈现畸变的八面体几何构型。而且该配合物通过氢键和π-π堆积作用扩展成三维超分子网状结构。此外还研究了它的荧光性质。
关键词: 锌配合物  晶体结构  荧光
基金项目: 
Abstract: A new coordination polymer [Zn(C2O4)(1,3-bix)]n (1, H2C2O4=oxalic acid, 1,3-bix=1,3-bis(imidazol-1-ylmethyl)-benzene) has been hydrothermally synthesized and structurally characterized by elemental analysis, IR spectrum, TG and single-crystal X-ray diffraction. The complex crystallizes in triclinic, space group P1 with a=0.885 8(2) nm, b=0.956 8(2) nm, c=1.019 6(3) nm, α=67.476(3)°, β=66.281(3)°, γ=77.280(3)°, V=0.780 0(3) nm3, C16H14N4O4Zn, Mr=391.68, Dc=1.668 g·cm-3, μ(Mo Kα)=1.605 mm-1, F(000)=400, Z=2, the final R=0.025 5 and wR=0.060 9 for 2 760 observed reflections (I>2σ(I)). In the crystal structure, the zinc atom is six-coordinated with four carboxylate oxygen atoms from two different C2O42- ligands and two nitrogen atoms from two different 1,3-bix ligands, showing a distorted octahedral geometry. Furthermore, it exhibits 3D supramolecular network structure through hydrogen bonding and π-π stacking interactions. Moreover, its luminescent property has been investigated in the solid state. CCDC: 908764.
Keywords: Zn(Ⅱ) complex  crystal structure  fluorescence
 
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战佩英,纪建业,牛艳玲,王志涛,李秀梅.以草酸及咪唑基配体构筑的二维网状锌(Ⅱ)配位聚合物的合成、晶体结构及荧光性质(英文)[J].无机化学学报,2013,29(2):424-428.
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