Carrasco, MarioMendoza, IreneAlvarez, EleuterioGrirrane, AbdessamadMaya, CeliaPeloso, RiccardoRodríguez, AmorFalceto Palacín, AndrésÁlvarez, Santiago (Álvarez Reverter)Carmona Guzmán, Ernesto2018-09-282018-09-282014-10-300947-6539https://hdl.handle.net/2445/124906To clarify the nature of the MoCarene interaction in terphenyl complexes with quadruple MoMo bonds, ether adducts of composition [Mo2(Ar′)(I)(O2CR)2(OEt2)] have been prepared and characterized (Ar′=ArXyl2, R=Me; Ar′=ArMes2, R=Me; Ar′=ArXyl2, R=CF3) (Mes=mesityl; Xyl=2,6‐Me2C6H3, from now on xylyl) and their reactivity toward different neutral Lewis bases investigated. PMe3, P(OMe)3 and PiPr3 were chosen as P‐donors and the reactivity studies complemented with the use of the C‐donors CNXyl and CN2C2Me4 (1,3,4,5‐tetramethylimidazol‐2‐ylidene). New compounds of general formula [Mo2(Ar′)(I)(O2CR)2(L)] were obtained, except for the imidazol‐2‐ylidene ligand that yielded a salt‐like compound of composition [Mo2(ArXyl2)(O2CMe)2(CN2C2Me4)2]I. The MoCarene interaction in these complexes has been analyzed with the aid of X‐ray data and computational studies. This interaction compensates the coordinative and electronic unsaturation of one of the Mo atoms in the above complexes, but it seems to be weak in terms of sharing of electron density between the Mo and Carene atoms and appears to have no appreciable effect in the length of the MoMo, MoX, and MoL bonds present in these molecules.13 p.application/pdfeng(c) Wiley-VCH, 2014MolibdèTeoria del funcional de densitatLligandsMolybdenumDensity functionalsLigandsinfo:eu-repo/semantics/article6442372018-09-28info:eu-repo/semantics/openAccess