SYNTHESIS, STRUCTURE, AND REACTIVITY OF RUTHENIUM AND OSMIUM NITRIDO COMPLEXES WITH 1,2-BENZENEDITHIOLATE LIGANDS - N-ALKYLATION VERSUS S-ALKYLATION

Citation
D. Sellmann et al., SYNTHESIS, STRUCTURE, AND REACTIVITY OF RUTHENIUM AND OSMIUM NITRIDO COMPLEXES WITH 1,2-BENZENEDITHIOLATE LIGANDS - N-ALKYLATION VERSUS S-ALKYLATION, Inorganic chemistry, 36(7), 1997, pp. 1397-1402
Citations number
69
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
36
Issue
7
Year of publication
1997
Pages
1397 - 1402
Database
ISI
SICI code
0020-1669(1997)36:7<1397:SSAROR>2.0.ZU;2-D
Abstract
The reactivity of the nitrido complexes (N(n)Bu(4))[Ru(N)(S2C6H4)(2)] (1) and ((NBU4)-B-n)[Os(N)(S2C6H4)(2)] (2) (C6H4(SH)(2) = 1,2-benzened ithiol) toward electrophiles, R(+) (R = Me, Et, Ph(3)C), is described. While 1 yielded intractable mixtures of products, 2 could be cleanly alkylated. The synthesis of 1 has been reported previously (Z. Naturfo rsch. 1987, 42B, 341); complex 2 can be synthesized by treating (N(n)B u(4))[Os(N)Cl-4] with deprotonated 1,2-benzenedithiol in acetone/MeOH at 0 degrees C. Complexes 1 and 2 are isostructural and crystallize in the orthorhombic space group Pna2(1), Z = 8, with a = 36.881(6) Angst rom, b = 9.402(2) Angstrom and c = 17.652(2) Angstrom for 1 and a = 37 .042(4) Angstrom, b = 9.375(2) Angstrom, and c = 17.671(2) Angstrom fo r 2. The anions of both compounds consist of a five-coordinate mononuc lear center with a distorted square-pyramidal geometry; a terminal nit rido Ligand occupies the apical position and two chelating (S2C6H4)(2- ) ligands form the basal plane. Treatment of 2 with R(3)OBF(4) in CH2C l2 yields [Os(N)(S2C6H4)(SC(6)H(4)SR)] (R = Me, 3; R = Et, 4) where on e thiolate donor is alkylated. Alkylation of the sulfur of the 1,2-ben zenedithiolate ligand was confirmed by NMR spectroscopy and X-ray crys tallography (for 3). Complex 3 . CH2Cl2 crystallizes in the orthorhomb ic space group P2(1)2(1)2(1), Z = 4, With a = 8.551(1) Angstrom, b = 1 0.772(2) Angstrom, and c = 19.716(3) Angstrom. In contrast, treatment of 2 with Ph(3)CPF(6) in CH2Cl2 yields [Os(NCPh(3))(S2C6H4)(2)] (5), w hose H-1 and C-13 NMR spectra indicate that the terminal nitride is th e site of electrophilic attack. X-ray crystallography further confirms the alkylation at the nitrogen atom; complex 5 crystallizes in the tr iclinic space group P1, Z = 2, with a = 9.338(8) Angstrom, b = 10.001( 3) Angstrom, c = 16.280(6) Angstrom, alpha = 75.88(3)degrees, beta = 7 4.29(6)degrees, and gamma = 69.55(5)degrees.