RT journal article
T1 Synthesis and Structure of Trinuclear W3S4 Clusters Bearing Aminophosphine Ligands and Their Reactivity toward Halides and Pseudohalides
A1 F. Beltrán, Tomás
A1 Pino-Chamorro, Jose Ángel
A1 Fernández-Trujillo Rey, María Jesús
A1 S. Safont, Vicent
A1 García Basallote, Manuel
A1 Llusar, Rosa
A2 Ciencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica
AB The aminophosphine ligand (2-aminoethyl)- diphenylphosphine (edpp) has been coordinated to the W3(μ-S)(μ-S)3 cluster unit to afford trimetallic complex [W3S4Br3(edpp)3]+ (1+) in a one-step synthesis process with high yields. Related [W3S4X3(edpp)3]+ clusters (X = F−, Cl−, NCS−; 2+−4+) have been isolated by treating 1+ with thecorresponding halide or pseudohalide salt. The structure of complexes 1+ to 4+ contains an incomplete W3S4 cubane-type cluster unit, and only one of the possible isomers is formed: the one with the phosphorus atoms trans to the capping sulfur and the amino groups trans to the bridging sulphurs. The remaining coordination position on each metal is occupied by X. Detailed studies using stopped-flow, 31P{1H} NMR, and ESI-MS have been carried out in order to understand the solution behavior and the kinetics of interconversion among species 1+, 2+, 3+, and 4+ in solution. Density functional theory (DFT) calculations have been also carried out on the reactions of cluster 1+ with the different anions. The whole set of experimental and theoretical data indicate that the actual mechanism of substitutions in these clusters is strongly dependent on the nature of the leaving and entering anions. The interaction between an entering F− and the amino group coordinated to the adjacent metal have also been found to be especially relevant to the kinetics of these reactions.
PB ACS Publications
YR 2015
FD 2015-12
LK http://hdl.handle.net/10498/20492
UL http://hdl.handle.net/10498/20492
LA eng
DS Repositorio Institucional de la Universidad de Cádiz
RD 15-nov-2026