204864-46-0Relevant academic research and scientific papers
Rhenium trichloride dioxide, ReO2Cl3
Supel, Joanna,Seppelt, Konrad
, p. 4675 - 4677 (2006)
(Figure Presented) Re-discovery: The only rhenium(VII)-chlorine compound known previously was ReO3Cl, and chloride oxides of composition AO2Cl3 (A = nonmetal or metal) were completely unknown. The synthesis of ReO2Cl3 has now been achieved. The compound exists as a chlorine-bridged dimer (see Figure; Re red, O blue, Cl green) in the solid state, and as a monomer in solution.
IMPROVED SYNTHESES OF TETRACHLORO-OXORHENIUM(VI) AND CHLOROTRIOXORHENIUM(VII). SYNTHESIS OF ALKOXO- AND DIALKYLAMIDO-RHENIUM COMPOUNDS. THE CRYSTAL AND MOLECULAR STRUCTURES OF DI-μ-METHOXOTETRAMETHOXO-μ-OXO-DIOXODIRHENIUM(VI) (Re-Re), BIS
Edwards, Peter G.,Wilkinson, Geoffrey,Hursthouse, Michael B.,Malik, K. M. Abdul
, p. 2467 - 2475 (2007/10/02)
Much improved synthetic procedures for ReOCl4, ReO3Cl, ReOMe4, Li2, and ReMe6 are described.Interaction of ReOCl4 with methanol in the presence of amine gives the unusual alkoxo-compound (MeO)2ORe(μ-O)(μ-OMe)2ReO(OMe)2, (A), while LiOBut gives ReO(OBut)4, and LiOPri gives an unusual dimeric species i)5>*LiCl(thf)2>2, (B) (thf = tetrahydrofuran).The interaction with phenol in the presence of trimethylphosphine leads to the compound trans-Re(OPh)4(PMe3)2, (C) while with lithium bis(trimethylsilyl)-amide a unique four-co-ordinate rhenium(V) compound, ReO3, is obtained.The crystal and molecular structures of (A)-(C) have been determined by X-ray crystallography.Compound (A) is monoclinic, space group P21/n, a = 12.142(1), b = 15.369(1), c = 7.311(1) Angstroem, β = 90.22(1)deg, and Z = 4.Compound (B) is triclinic, space group P1, a = 14.602(5), b = 13.363(3), c = 9.244(6) Angstroem, α = 98.39(4), β = 102.35(5), γ = 68.71(2)deg, and Z = 1.Compound (C) is monoclinic, space group P21/c, a = 10.079(2), b = 10.527(3), c = 14.443(3) Angstroem, β = 97.28(2) deg, and Z = 2.The structures have been refined to R values of 0.059 (A), 0.069(B)' and 0.055 (C) using respectively 1965, 4061, and 1797 observed intensities, measured on a diffractometer.
Edwards, Peter G.,Wilkinson, Geoffrey,Hursthouse, Michael B.,Malik, K. M. Abdul
, p. 2467 - 2475 (2007/10/02)
Much improved synthetic procedures for ReOCl4, ReO3Cl, ReOMe4, Li2, and ReMe6 are described.Interaction of ReOCl4 with methanol in the presence of amine gives the unusual alkoxo-compound (MeO)2ORe(μ-O)(μ-OMe)2ReO(OMe)2, (A), while LiOBut gives ReO(OBut)4, and LiOPri gives an unusual dimeric species i)5>*LiCl(thf)2>2, (B) (thf = tetrahydrofuran).The interaction with phenol in the presence of trimethylphosphine leads to the compound trans-Re(OPh)4(PMe3)2, (C) while with lithium bis(trimethylsilyl)-amide a unique four-co-ordinate rhenium(V) compound, ReO3, is obtained.The crystal and molecular structures of (A)-(C) have been determined by X-ray crystallography.Compound (A) is monoclinic, space group P21/n, a = 12.142(1), b = 15.369(1), c = 7.311(1) Angstroem, β = 90.22(1)deg, and Z = 4.Compound (B) is triclinic, space group P1, a = 14.602(5), b = 13.363(3), c = 9.244(6) Angstroem, α = 98.39(4), β = 102.35(5), γ = 68.71(2)deg, and Z = 1.Compound (C) is monoclinic, space group P21/c, a = 10.079(2), b = 10.527(3), c = 14.443(3) Angstroem, β = 97.28(2) deg, and Z = 2.The structures have been refined to R values of 0.059 (A), 0.069(B)' and 0.055 (C) using respectively 1965, 4061, and 1797 observed intensities, measured on a diffractometer.
