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首页> 外文期刊>Inorganica Chimica Acta >Zinc maleate and fumarate coordination polymers containing hydrogen-bonding capable organodiimines featuring ligand dependent in situ cis–trans isomerization
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Zinc maleate and fumarate coordination polymers containing hydrogen-bonding capable organodiimines featuring ligand dependent in situ cis–trans isomerization

机译:马来酸锌和富马酸酯配位聚合物,含有能与氢键结合的有机二亚胺,其特征在于依赖于配体的原位顺反异构

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摘要

Solution phase reaction at ambient temperature of zinc nitrate, maleic acid and 4,40-dipyridylamine (dpa) afforded {[Zn2(maleate)2(dpa)2]5H2O}n (1), which displayed parallel (4,4)-grid like coordination polymer layers interdigitated into double layer slab motifs via hydrogen bonding. A similar reaction employing bis(4-pyridylmethyl)piperazine (bpmp) caused in situ cis–trans isomerization of maleic acid to fumarate, and generation of [Zn(fumarate)(bpmp)(H2O)2]n (2). Compound 2 also manifested (4,4)-grid coordination polymer layers similar to those in 1; however, the larger apertures in 2 permit 2d + 2d?3D mutually inclined interpenetration. Thermogravimetric and luminescence studies are also reported for 1 and 2.
机译:在环境温度下,硝酸锌,马来酸和4,40-二吡啶胺(dpa)的溶液相反应产生{[Zn2(马来酸酯)2(dpa)2] 5H2O} n(1),显示平行(4,4)-网格状配位聚合物层通过氢键交叉成双层平板图案。使用双(4-吡啶基甲基)哌嗪(bpmp)的类似反应引起马来酸原位顺式-反式异构化为富马酸酯,并生成[Zn(富马酸酯)(bpmp)(H2O)2] n(2)。化合物2还表现出与1相似的(4,4)-网格配位聚合物层。但是,2中较大的孔允许2d + 2d?3D相互倾斜的互穿。还报道了1和2的热重和发光研究。

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