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Hydrothermal syntheses, structures and luminescent properties of group IIB metal coordination polymers based on bifunctional 1H-tetrazolate-5-acetic acid ligand

机译:基于双官能1H-四唑酸酯-5-乙酸配体的IIB族金属配位聚合物的水热合成,结构和发光性能

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摘要

Hydrothermal reaction of 1H-tetrazolate-5-ethyl acetate (Htzea), MCl2 (M = Zn, Cd) and NaOH at different reaction temperatures produced three new coordination polymers: 2-D layered polymer [Zn(tza)(H2O)2]_n 1, and 1-D chained supramolecular isomers 2 and 3 formulated as [Cd(tza)(H2O)2]_n (H2tza = 1H-tetrazo-late-5-acetic acid), respectively. In these obtained polymers, tza~(2-) ligand adopts variable coordination modes: μ3-kN3:kO1:k:O2,N1 and μ3-kN1:kN3:kO2 for 1, and μ3-kN2:kN1,O2:kO1,O2 for 2 and 3. The effects of reaction temperature and metal centers on the final polymeric frameworks have been discussed. Polymers 1-3 exhibit blue photoluminescence mainly arising from intraligand transitions of tet-razolate rings in tza~(2-) ligand.
机译:1H-四唑基-5-乙酸乙酯(Htzea),MCl2(M = Zn,Cd)和NaOH在不同反应温度下的水热反应产生了三种新的配位聚合物:2-D层状聚合物[Zn(tza)(H2O)2] _n 1和1-D链状超分子异构体2和3分别配制为[Cd(tza)(H2O)2] _n(H2tza = 1H-四唑基--5-乙酸)。在这些获得的聚合物中,tza〜(2-)配体采用可变配位模式:μ3-kN3:kO1:k:O2,N1和μ3-kN1:​​kN3:kO2表示1,μ3-kN2:kN1,O2:kO1, O 2为2和3。已经讨论了反应温度和金属中心对最终聚合物骨架的影响。聚合物1-3显示出蓝色的光致发光,主要由tza-(2-)配体中的tet-razolate环的配体内过渡引起。

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