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Osmium Complexes of 1,4,7-Triazacyclononane (tacn) and 1,4,7-Trimethyl-1,4,7-triazacyclononane (Me(3)tacn) and the X-ray Crystal Structure of [(Me(3)tacn)Os(eta(6)-C(6)H(5)BPh(3))]BPh(4).CH(3)CN
Authors:Ware David C  Olmstead Marilyn M  Wang Renyi  Taube Henry
Institution:Departments of Chemistry, Stanford University, Stanford, California 94305, University of Auckland, Private Bag 92019, Auckland, New Zealand, and University of California, Davis, California 95616.
Abstract:The complexes of osmium with tacn (1,4,7-triazacyclononane) and Me(3)tacn (1,4,7-trimethyl-1,4,7-triazacyclononane), LOs (eta(6)-C(6)H(6))](PF(6))(2) (L = tacn) and LOsCl(3) (L = tacn, Me(3)tacn), have been prepared by substitution of L on Os(eta(6)-C(6)H(6))Cl(2)](2) or Os(2)Cl(8)](2)(-), respectively. Reaction of LOsCl(3) with neat triflic acid leads to partial replacement of chloride and formation of the binuclear Os(III)-Os(III) complexes LOs(&mgr;-Cl(3))OsL](PF(6))(3) (L = tacn, Me(3)tacn). The binuclear nature was established by NMR spectroscopy and elemental analysis and, for L = tacn, a partially refined X-ray crystal structure which shows the Os-Os separation to be 2.667 ?, indicative of significant metal-metal bonding. Reduction of LOs(&mgr;-Cl(3))OsL](3+) over zinc amalgam in either aqueous or non-aqueous solution yields the intensely colored Os(II)-Os(III) mixed-valence ions LOs(&mgr;-Cl(3))OsL](2+). Electrochemical measurements on LOs(&mgr;-Cl(3))OsL](3+) in CH(3)CN reveal the reversible formation of the mixed valence ions. These are further reduced at lower potential to the Os(II)-Os(II) binuclear species, reversibly for L = Me(3)tacn. (Me(3)tacn)OsCl(3) is oxidized by persulfate ion to give (Me(3)tacn)OsCl(3)](+); zinc amalgam reduction in an aqueous solution at high concentration produces the binuclear complex (Me(3)tacn)Os(&mgr;-Cl(3))Os(Me(3)tacn)](3+) or, at low concentration, a solution containing an air sensitive osmium(II) species. Addition of BPh(4)(-) results in the eta(6)-arene zwitterion (Me(3)tacn)Os(eta(6)-C(6)H(5)BPh(3))](+), which was characterized by X-ray diffraction on the BPh(4)(-) salt. The compound crystallizes in the triclinic space group P1 with a = 11.829(2) ?, b = 12.480(3) ?, c = 17.155(4) ?, alpha = 84.42(2) degrees, beta = 83.52(2) degrees, gamma = 71.45(2) degrees, V = 2380(2) ?(3), Z = 2, and R = 7.62%, and R(w) = 7.39%.
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