Cycloaddition of alkynes to diimino Mo3S4 cubane-type clusters: a combined experimental and theoretical approach
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Author/sGarcía Algarra, Andrés; Pino-Chamorro, Jose Ángel; A. Laricheva, Yuliya; Guillamón, Eva; Fernández-Trujillo Rey, María Jesús; Bustelo, Emilio; L. Gushchin, Artem; Y. Shmelev, Nikita; A. Abramov, Pavel; N. Sokolov, Maxim; Llusar, Rosa; García Basallote, Manuel
DepartmentCiencia de los Materiales e Ingeniería Metalúrgica y Química Inorgánica
SourceNew Journal of Chemistry 2016, 40, 7872--7880
A heterocyclic ligand 4,40-di-tert-butyl-2,20-bipyridine (dbbpy) has been coordinated to the Mo3S4 cluster unit affording the complex [Mo3S4Cl3(dbbpy)3]+ (+) in a one-step ligand-exchange protocol from [Mo3S4(tu)8(H2O)]Cl4 4H2O (tu = thiourea). The new cluster was isolated as PF6 and Cl salts in high yields and the crystal structure of the latter determined by X-ray analysis. The synthetic procedure was extended to tungsten to afford [W3S4Cl3(dbbpy)3]+ (+). Kinetic and NMR studies show that + reacts with several alkynes to form dithiolene species via concerted [3+2] cycloaddition reactions whereas + remains inert under similar conditions. The different rates for the reactions of + are rationalised by computational (DFT) calculations, which show that the more electron-withdrawing the substituents of the alkyne the faster the reaction. The inertness of + is due to the endergonicity of its reactions, which feature DGr values systematically 5–7 kcal mol 1 more positive than for those of +.