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Título

H3O2 bridging ligand in a metal-organic framework. Insight into the Aqua-Hydroxo↔hydroxyl equilibrium: A combined experimental and theoretical study

AutorVries, Richard F. de ; Peña O'Shea, Víctor A. de la; Snejko, Natalia ; Iglesias, Marta ; Gutiérrez-Puebla, Enrique ; Monge, M. Ángeles
Fecha de publicación2013
EditorAmerican Chemical Society
CitaciónJournal of the American Chemical Society 135(15): 5782-5792 (2013)
ResumenA metal-organic framework (MOF) bearing the aqua-hydroxo species (O 2H3)- in the framework, as well as the processes that govern the equilibrium aqua-hydroxo (O2H 3)-↔hydroxyl (OH) in Sc-MOFs, are studied experimentally and theoretically. Computational studies were employed to determine the relative energies for the two compounds that coexist under certain hydrothermal conditions at pH < 2.8. The thermodynamically more stable [Sc3(3,5-DSB)2(μ-O2H3)(μ-OH) 2(H2O)2] (from now on, (O2H 3)Sc-MOF; 3,5-DSB = 3,5-disulfobenzoic acid) was obtained as a pure and stable phase. It was impossible to isolate [Sc3(3,5-DSB) 2(μ-OH)3(H2O)4] as a pure phase, as it turned out to be the precursor of (O2H3)Sc-MOF. Additionally, a third compound that appears at pH between 3.5 and 4, [Sc 3(3,5-DSB)(μ-OH)6(H2O)] and a fourth, [Sc(3,5-DSB)(Phen)(H2O)](H2O), in whose formula neither OH groups nor H3O2 - anions appear, are reported for comparative purposes. A study of the (O2H3)Sc-MOF electronic structure, and some heterogeneous catalytic tests in cyanosilylation of aldehydes reactions, are also reported. © 2013 American Chemical Society.
URIhttp://hdl.handle.net/10261/94335
DOI10.1021/ja4005046
Identificadoresdoi: 10.1021/ja4005046
issn: 0002-7863
e-issn: 1520-5126
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