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Coordination Behavior of Chelidamic Acid With VV, NiII, FeIII, and CaII: Syntheses, X-ray Characterization and DFT Studies

机译:Chelidamic与VV,NIII,FEIII和CAI的协调行为:合成,X射线表征和DFT研究

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摘要

Four new complexes of chelidamic acid (H3cda) in the presence of 2-aminopyrimidine (apym) or 2,4,6-triamino-1,3,5-triazine (tata) as external ligands, namely (apymH)[VO2(Hcda)]·H2O (1), [Ni(Hcda)(apym)(H2O)2]·H2O (2), (apymH)[Fe(Hcda)2] (3), and (tataH) 2(tata)2[Ca2(cda)2(H2O)6]·H2O (4) were synthesized. X-ray diffraction analysis of 1-4 revealed the formation of 3D frameworks generally involving weak interactions (mainly H-bonds) between metal complexes of chelidamic acid, protonated or deprotonated external ligands apym or tata and co-crystallized water molecules. Some complexes present remarkable assemblies in the solid state governed by unconventional noncovalent interactions that have been analyzed by means of DFT calculations. Solution studies were also performed to fully characterize the new compounds.
机译:在存在2-氨基嘧啶(APYM)或2,4,6- triamino-1,3,5-三嗪(TATA)的情况下,螯合剂酸(H3CDA)的四个新复合物(H3CDA)作为外配体,即(apymh) )·H2O(1),[ni(hcda)(apym)(h2o)2]·H2O(2),(apymh)[fe(hcda)2] 2](3)(3)和(tatah)2(tata)2(tata)2 [Ca2(CDA)2(H2O)6]·H2O(4)合成。 对1-4的X射线衍射分析表明,在Chelidamic酸的金属络合物,质子化或去质子化的外配体APYM或TATA以及共结晶的水分子之间,通常涉及弱相互作用(主要是H键)的3D框架的形成。 一些复合物在固态中表现出了显着的组合,由非常规非共价相互作用控制,这些相互作用已通过DFT计算进行了分析。 还进行了溶液研究以充分表征新化合物。

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