School of Chemistry, University of Bristol, Cantock's Close, Bristol, BS8 1TS, UK.
Institute of Chemistry, University of Tartu, Ravila 14a, Tartu, 50411, Estonia.
Chemistry. 2022 Oct 21;28(59):e202202247. doi: 10.1002/chem.202202247. Epub 2022 Aug 17.
A molecular system comprising a cationic zinc complex and an amino acid-derived ambident ligand having phosphate and carboxylate binding sites undergoes a series of rearrangements in which the metal cation migrates autonomously from one site to another. The location of the metal is identified by the circular dichroism spectrum of a ligated bis(2-quinolylmethyl)-(2-pyridylmethyl)amine (BQPA) chromophore, which takes a characteristic shape at each binding site. Migration is fuelled by the decomposition of trichloroacetic acid to CO and CHCl , which progressively neutralises the acidity of the system as a function of time, revealing in sequence binding sites of increasing basicity. The migration rate responds to control by variation of the temperature, water content and triethylamine concentration, while an excess of fuel controls the duration of an induction period before the migration event.
一个由阳离子锌配合物和一个具有磷酸和羧酸盐结合位点的氨基酸衍生的两性配体组成的分子体系经历了一系列的重排,其中金属阳离子自主地从一个位点迁移到另一个位点。金属的位置通过配位的双(2-喹啉基甲基)-(2-吡啶基甲基)胺(BQPA)发色团的圆二色性光谱来确定,该发色团在每个结合位点呈现出特征形状。迁移是由三氯乙酸分解为 CO 和 CHCl 3 驱动的,随着时间的推移,三氯乙酸逐渐中和体系的酸度,依次揭示出碱性逐渐增强的结合位点。迁移率可以通过改变温度、含水量和三乙胺浓度来控制,而过量的燃料可以控制迁移事件前诱导期的持续时间。