Oliveri Anna F, Colla Christopher A, Perkins Cory K, Akhavantabib Noushin, Callahan Joseph R, Pilgrim Corey D, Smart Scott E, Cheong Paul H-Y, Pan Long, Casey William H
Department of Chemistry, University of California, 1 Shields Ave, Davis, CA, 95616, USA.
Department of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, OR, 97331, USA.
Chemistry. 2016 Dec 23;22(52):18682-18685. doi: 10.1002/chem.201604640. Epub 2016 Nov 23.
The solution chemistry of aluminum has long interested scientists due to its relevance to materials chemistry and geochemistry. The dynamic behavior of large aluminum-oxo-hydroxo clusters, specifically [Al O (OH) (H O) ] (Al ), is the focus of this paper. Al NMR, H NMR, and H DOSY techniques were used to follow the isomerization of the ϵ-Al in the presence of glycine and Ca at 90 °C. Although the conversion of ϵ-Al to new clusters and/or Baker-Figgis-Keggin isomers has been studied previously, new H NMR and H DOSY analyses provided information about the role of glycine, the ligated intermediates, and the mechanism of isomerization. New H NMR data suggest that glycine plays a critical role in the isomerization. Surprisingly, glycine does not bind to Al clusters, which were previously proposed as an intermediate in the isomerization. Additionally, a highly symmetric tetrahedral signal (δ=72 ppm) appeared during the isomerization process, which evidence suggests corresponds to the long-sought α-Al isomer in solution.
铝的溶液化学长期以来一直吸引着科学家,因为它与材料化学和地球化学相关。大型铝-氧-氢氧根簇的动态行为,特别是[Al O (OH) (H O) ] (Al ),是本文的重点。采用Al NMR、 H NMR和 H DOSY技术跟踪在90 °C下甘氨酸和Ca存在时ϵ-Al的异构化。尽管之前已经研究了ϵ-Al向新簇和/或贝克-菲吉斯-凯gin异构体的转化,但新的 H NMR和 H DOSY分析提供了有关甘氨酸的作用、配位中间体以及异构化机制的信息。新的 H NMR数据表明甘氨酸在异构化中起关键作用。令人惊讶的是,甘氨酸不与之前被认为是异构化中间体的Al簇结合。此外,在异构化过程中出现了一个高度对称的四面体信号(δ=72 ppm),有证据表明它对应于溶液中长期寻找的α-Al异构体。