化学
配位复合体
甲醇
螯合作用
铟
水溶液
拉曼光谱
光谱学
胺气处理
分子
核磁共振波谱
配位几何学
无机化学
药物化学
立体化学
金属
有机化学
氢键
量子力学
物理
光学
作者
Concepción Avila‐Montiel,Hugo Tlahuext,Armando Ariza‐Castolo,Carolina Godoy‐Alcántar,Antonio R. Tapia‐Benavides,Margarita Tlahuextl
标识
DOI:10.1002/ejic.202200178
摘要
Abstract We report the synthesis of eight indium coordination compounds derived from amino amides 1 – 8 and InCl 3 . Crystallographic and NMR studies revealed the unusual chelation coordination of the metal ion to the amine and carbonyl groups of the ligands. However, vibrational studies evidenced the presence of formation‐breaking equilibria of the C=O→In 3+ coordination bond. Thus, as chelate structures predominate in methanol solutions, In 3+ compounds with open structures prevail in aqueous solutions. Moreover, the Raman spectroscopy and crystallography studies of 2 c and 6 c corroborated that the substitution of a chlorine ion by a methanol molecule in these coordination compounds is feasible and that the interchange equilibrium [H L ]InCl 4 +MeOH⇄[ L ][MeOH]InCl 3 +HCl is present in methanolic solutions. UV spectroscopy proves that the [H L ]InCl 4 compounds predominates in methanol solutions. However, fluorescence spectroscopy shows the presence of significant quantities of [ L ][MeOH]InCl 3 that reduce the intensity of the signals. The formation‐breaking and interchange equilibria could facilitate the biological interchange of In 3+ using coordination compounds 1 c – 8 c .
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