含氮辅助配体刚性变化调节萘二膦酸镉配合物结构
Structure variation of cadmium naphthalene-diphosphonates with the changing rigidity of N-donor auxiliary ligands
作者单位E-mail
徐艳 宿迁学院生物与材料工程学院化学系, 宿迁 223800 17101@squ.edu.cn 
李素芝 宿迁学院生物与材料工程学院化学系, 宿迁 223800 lisuzhi2005@sina.com 
李艳 宿迁学院生物与材料工程学院化学系, 宿迁 223800  
冯路顺 宿迁学院生物与材料工程学院化学系, 宿迁 223800  
孙文韬 宿迁学院生物与材料工程学院化学系, 宿迁 223800  
李新星 宿迁学院生物与材料工程学院化学系, 宿迁 223800  
摘要: 在水热条件下,从萘二膦酸配体出发,通过调控辅助配体的刚性,采用配位竞争策略,合成了5种金属萘二膦酸镉配合物:[Cd1.5(1,4-ndpaH2)2(4,4'-bpyH)(4,4'-bpy)0.5(H2O)2]2(1)、[Cd (1,4-ndpaH2)(1,4-bib)0.5(H2O)](2)、[Cd (1,4-ndpaH3)2(1,2-dpe)(H2O)]·(1,2-dpe)·7H2O (3)、(1,2-bixH)[Cd3(1,4-ndpaH)(1,4-ndpaH2)2(H2O)2](4)和[Cd (1,4-ndpaH2)(H2O)]·H2O (5),其中1,4-ndpaH4=1,4-萘二膦酸,4,4'-bpy=4,4'-联吡啶,1,4-bib=1,4-双(1-咪唑基)苯,1,2-dpe=1,2-二(4-吡啶基)乙烯,1,2-bix=双(咪唑-1-基甲基)苯。单晶X射线衍射结构解析显示,配合物1具有层状结构,其中{Cd3(PO2)2}三核单元由共角的2个{CdO4N2}和1个{CdO6}八面体组成,膦酸基团连接{Cd3(PO2)2}三核单元,形成带状结构,刚性4,4'-bpy配体将其交联成二维层状结构。配合物2为三维开放骨架结构,三角双锥体{CdO4N}通过O—P—O桥联成一维链,相邻的链通过刚性的1,4-bib或萘二膦酸配体交联,形成三维结构。配合物3具有一维双金属梯形链结构,由八面体{CdO5N}通过1,4-ndpaH22-连接成一维链,相邻链的金属离子之间再通过1,4-ndpaH22-配体进一步连接成梯形结构,半刚性的1,2-dpe或是以单侧配位悬挂于梯形链的两侧或是以客体分子内嵌于晶体骨架中。通过引入柔性配体1,2-bix或1,3-二(4-吡啶基)丙烷(1,3-dpp)合成得到的配合物4和5均显示出由1,4-ndpaH22-配体交联双金属链的二维层状结构,有趣的是,配合物4中柔性1,2-bix分子单质子化且以客体分子的形式填充于层与层之间,而配合物5的结构中并未出现合成过程中添加的柔性配体1,3-dpp。光学性质研究表明配合物1~5显示出配体中心的光致发光性质。
关键词: 萘二膦酸  含氮辅助配体  晶体结构  刚性  柔性
基金项目: 宿迁市科技计划项目(No.Z202376)、江苏省青蓝工程、宿迁学院科研平台(No.2021pt04)和宿迁学院西楚高层次人才资助。
Abstract: Five cadmium naphthalene-diphosphonates, formulated as [Cd1.5(1,4-ndpaH2)2(4,4'-bpyH)(4,4'-bpy)0.5 (H2O)2]2 (1), [Cd(1,4-ndpaH2)(1,4-bib)0.5(H2O)] (2), [Cd(1,4-ndpaH3)2(1,2-dpe)(H2O)]·(1,2-dpe)·7H2O (3), (1,2-bixH) [Cd3(1,4-ndpaH)(1,4-ndpaH2)2(H2O)2] (4), and [Cd(1,4-ndpaH2)(H2O)]·H2O (5), have been synthesized from the selfassembly reactions of 1,4-naphthalenediphosphonic acid (1,4-ndpaH4) with Cd(NO3)2·4H2O by introducing auxiliary ligands with variation of rigidity, such as 4,4'-bipyridine (4,4'-bpy), 1,4-bis(1-imidazolyl)benzene (1,4-bib), 1,2-di(4pyridyl)ethylene (1,2-dpe), 1,3-di(4-pyridyl)propane (1,3-dpp), and bis(imidazol-1-ylmethyl)benzene (1,2-bix), respectively. Structure resolution by single crystal X ray diffraction reveals that compound 1 possesses a layered framework, in which the {Cd3(PO2)2} trimers made up of corner-sharing two {CdO4N2} and one {CdO6} octahedra are connected by phosphonate groups, forming a ribbon, which are cross-linked by 4,4'-bipy ligands, forming a 2D layer. Compound 2 shows a 3D open-framework structure, where chains of corner-sharing {CdO4N} trigonal bipyramids and {PO3C} tetrahedra are cross-linked by 1,4-bib and/or phosphonate groups. A 1D ladder-like chain structure is found in compound 3, where the ladder-like chains made up of corner-sharing {CdO5N} octahedra and {PO3C} tetrahedra are connected by 1,4-ndpaH22-. Both compounds 4 and 5 obtained by the introduction of flexible ligands during the synthesis show a 2D layered structure, which is formed by ligand crosslinking double metal chains. Interestingly, In 4, flexible 1,2-bix was singly protonated, as guest molecules, filled between layer and layer, while flexible ligand 1,3-dpp is absent in 5. Photophysical measurements indicate that compounds 1-5 show ligand-centered emissions.
Keywords: naphthalene diphosphate  N-donor auxiliary ligands  crystal structure  rigidity  flexibility
投稿时间:2024-06-17 修订日期:2024-09-05
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徐艳,李素芝,李艳,冯路顺,孙文韬,李新星.含氮辅助配体刚性变化调节萘二膦酸镉配合物结构[J].无机化学学报,2025,41(2):395-406.
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