533880-58-9Relevant academic research and scientific papers
Competitive O-H and C-H oxidative addition of CH3OH to rhodium(II) porphyrins
Li, Shan,Cui, Weihong,Wayland, Bradford B.
, p. 4024 - 4025 (2008/03/18)
Rhodium(II) porphyrins react with CH3OH in benzene by alternate mechanisms that give H-CH2OH and H-OCH3 bond activation in different methanol concentration regimes which is a rare example of transition metal reactivity with methanol. The Royal Society of Chemistry.
Bimetallo-radical carbon-hydrogen bond activation of methanol and methane
Cui, Weihong,Zhang, X. Peter,Wayland, Bradford B.
, p. 4994 - 4995 (2007/10/03)
Carbon-hydrogen bond cleavage reactions of CH3OH and CH4 by a dirhodium(II) diporphyrin complex with a m-xylyl tether (·Rh(m-xylyl)Rh·(1)) are reported. Kinetic-mechanistic studies show that the substrate reactions are bimolecular and occur through the use of two Rh(II) centers in the molecular unit of 1. Second-order rate constants (T = 296 K) for the reactions of 1 with methanol (k(CH3OH) = 1.45 × 10-2 M-1 s-1) and methane (k(CH4) = 0.105 M-1 s-1) show aclear kinetic preference for the methane activation process. The methanol and methane reactions with 1 have large kinetic isotope effects (k(CH3OH)/k(CD3OD) = 9.7 ± 0.8, k(CH4)/k(CD4) = 10.8 ± 1.0, T = 296 K), consistent with a rate-limiting step of C-H bond homolysis through a linear transition state. Activation parameters for reaction of 1 with methanol (ΔH = 15.6 ± 1.0 kcal mol-1; ΔS = -14 ± 5 cal K-1 mol-1) and methane (ΔH = 9.8 ± 0.5 kcal mol-1; ΔS = -30 ± 3 cal K-1 mol-1) are reported. Copyright
