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In situ deaminization reaction of the D-3-(4-Pyridyl)-alanine: A chiral zigzag chain and a five-fold interpenetrated diamondoid network

机译:D-3-(4-吡啶基)-丙氨酸的原位脱氨反应:手性曲折链和五倍互穿的类金刚石网络

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摘要

The reaction of Cu(NO3)2·3H2O/Zn(NO3)2·6H2O and D-3-(4-Pyridyl)-alanine (Hpyala) without or with 4,4'-bipyridine (bpy) leads to the generation of two new coordination polymers, [Cu(pyaIa)2]·H2O (1) and [Zn(4-pyridylacrylate)2]·H2O (2). Interestingly, the 4-pyridyacrylate ligand was derived from the in situ deaminization of the D-3-(4-Pyridyl)-alanine under the hydrothermal conditions. Single-crystal X-ray diffraction studies indicate that 1 exhibits a one-dimensional (1D) chiral chain structure; 2 exhibits 3D framework with 5-fold interpenetrated diamondoid topology, which contains open channels occupied by the lattice water molecules.
机译:Cu(NO3)2·3H2O / Zn(NO3)2·6H2O与D-3-(4-吡啶基)-丙氨酸(Hpyala)的反应在没有或有4,4'-联吡啶(bpy)的情况下导致两种新的配位聚合物[Cu(pyaIa)2]·H2O(1)和[Zn(4-吡啶基丙烯酸酯)2]·H2O(2)。有趣的是,4-吡啶丙烯酸酯配体是在水热条件下从D-3-(4-吡啶基)-丙氨酸的原位脱氨得到的。单晶X射线衍射研究表明1表现出一维(1D)手性链结构;图2展示了具有5倍互穿菱形拓扑的3D框架,其中包含由晶格水分子占据的开放通道。

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