Nucleophilic reactivity and oxo/sulfido substitution reactions of MVIO3 Groups (M = Mo, W).

The nucleophilic reactivity of oxo ligands in the groups M(VI)O(3) in the trigonal complexes [(Me(3)tacn)MO(3)] (M = Mo (1), W (10)) and [(Bu(t)(3)tach)MO(3)] (M = Mo (5), W (14)) has been investigated. Complexes 1/10 can be alkylated with MeOTf to give (Me(3)tacn)MO(2)(OMe) (2/11), silylated with Pr(i)(3)SiOTf to form (Me(3)tacn)MO(2)(OSiPr(i)(3)) (3/12), and protonated with HOTf to yield (Me(3)tacn)MoO(2)(OH) (4). Similarly, complexes 5/14 can be silylated to (Bu(t)(3)tach)MO(2)(OSiPr(i)(3)) (6/15) and protonated to (Bu(t)(3)tach)MO(2)(OH) (7/16). Products were isolated as triflate salts in yields exceeding 70%. When excess acid was used, the dinuclear mu-oxo species (Bu(t)(3)tach)(2)M(2)O(5) (8/17) were obtained. X-ray structures are reported for 2-4, 6-8, 12, and 15-17. All mononuclear complexes have dominant trigonal symmetry with a rhombic distortion owing to a M[bond]OR bond (R = Me, SiPr(i)(3), H), which is longer than M[double bond]O oxo interactions; the latter exert a substantial trans influence on M[bond]N bond lengths. Oxo ligands in 5/14 undergo replacement with sulfide. Lawesson's reagent effects formation of [(Bu(t)(3)tach)MS(3)] (9/18), 14 with excess B(2)S(3) yields incompletely substituted [(Bu(t)(3)tach)WOS(2)] (20), and 5 with excess B(2)S(3) yields [(Bu(t)(3)tach)Mo(IV)O(S(4))] (19). The structures of 9, 19, and 20 are reported. Precedents for M(VI)S(3) groups in five- and six-coordinate molecules are limited. This investigation is the first detailed study of the behavior of M(VI)O(3) groups in nucleophilic and oxo/sulfido substitution reactions and should be useful in synthetic approaches to the active sites of the xanthine oxidase enzyme family and of certain tungstoenzymes. (Bu(t)(3)tach = 1,3,5-tri-tert-butyl-1,3,5-triazacyclohexane, Me(3)tacn = 1,4,7-trimethyl-1,4,7-triazacyclonane; OTf = triflate).