Structural diversity and luminescent sensing of three coordination polymers based on the hydrolysates of N,N′-bis(3,5-dicarboxylatophenyl)pyromelliticdi-imide)

被引:3
作者
Fan, Liming [1 ]
Wang, Jiang [1 ]
Zhao, Li [1 ]
Zhang, Yujuan [1 ]
Wang, Xiaoqing [1 ]
Hu, Tuoping [1 ]
Zhang, Xiutang [2 ]
机构
[1] North Univ China, Coll Sci, Dept Chem, Taiyuan 030051, Peoples R China
[2] Qilu Normal Univ, Coll Chem & Chem Engn, Adv Mat Inst Res, Jinan 250013, Shandong, Peoples R China
关键词
Hydrolysis mechanism; In-situ reaction; Structural diversity; Self-assembly; Luminescent sensing; METAL-ORGANIC FRAMEWORKS; LIGAND; MOFS; COMPLEXES; CATALYSTS; CHANNELS; SITES; SBU;
D O I
10.1016/j.molstruc.2018.05.092
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Based on the hydrolysates of N,N'-bis(3,5-dicarboxylatophenyl)pyromelliticdi-imide) (H4L) and 1,3-bis(imidazol-1-ylmethyl)benzene (bimb), three coordination polymers, namely, {[Zn(BTC)(0.5)(bimb)]center dot 4H(2)O)(n) (1), [Cu(BTC)(0.5)(bimb)](n) (2), and {[Cd(AIP)(H2O)]center dot H2O)(n) (3), have been obtained under solvothermal conditions. The possible hydrolysis mechanism of H4L. was investigated here. Structural analyses reveal that complex I is a 3D (4,4)-c {6(4).8(2)}{6(6)}(2)-bbf net. Complex 2 displays a 2D 4-c {3(2).6(2).7(2)}-kgm sheet. While complex 3 exhibits a 3D (3,6)-c {4.6(2)}(2)[4(2).6(10).8(3)}-rtl net based on binuclear {Cd-2(COO)(4)) SBUs. Besides, luminescent sensing investigation indicated that 1 and 3 exhibit highly sensitive and selective sensing of chromate anions in aqueous solution. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:54 / 61
页数:8
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