2006Journal of Chemical ResearchRequires access

Kinetics of Oxidation of 1,4-Butylene Glycol by Dihydroxydiperiodatoargentate(III) in Alkaline Medium

Jinhuan Shan, Shengmin Li, Shuying Huo, Wenjie Zhao, Shigang Shen, Hanwen Sun

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Abstract

Kinetics of oxidation of 1,4-butylene glycol by dihydroxydiperiodatoargentate(III) in alkaline liquid has been investigated by spectrophotometry in the 298.2–318.2K range. The order in oxidant was pseudo first order and the order with respect to 1,4-butylene glycol was 1< n ap <2. The associated rate law was: –d[Ag(III)] t /dt = { kK 1 K 2 [OH - ][HOCH 2 CH 2 CH 2 CH 2 OH] 2 [Ag(III)] t }/{[H 2 IO 4 3- ] + K 1 [OH - ] + K 1 K 2 [OH - ][HOCH 2 CH 2 CH 2 CH 2 OH]} = k obs [Ag(III)] t . A plausible mechanism involving a pre-equilibrium of adduct formation between the complex and reductant was proposed. The activation parameters along with rate constants of the rate-determining step were calculated.

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Kinetics of oxidation of 1,4-butylene glycol by dihydroxydiperiodatoargentate(III) in alkaline liquid has been investigated by spectrophotometry in the 298.2–318.2K range. The order in oxidant was pseudo first order and the order with respect to 1,4-butylene glycol was 1< n ap <2. The associated rate law was: –d[Ag(III)] t /dt = { kK 1 K 2 [OH - ][HOCH 2 CH 2 CH 2 CH 2 OH] 2 [Ag(III)] t }/{[H 2 IO 4 3- ] + K 1 [OH - ] + K 1 K 2 [OH - ][HOCH 2 CH 2 CH 2 CH 2 OH]} = k obs [Ag(III)] t . A plausible mechanism involving a pre-equilibrium of adduct formation between the complex and reductant was proposed. The activation parameters along with rate constants of the rate-determining step were calculated.

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Available abstract

Kinetics of oxidation of 1,4-butylene glycol by dihydroxydiperiodatoargentate(III) in alkaline liquid has been investigated by spectrophotometry in the 298.2–318.2K range. The order in oxidant was pseudo first order and the order with respect to 1,4-butylene glycol was 1< n ap <2. The associated rate law was: –d[Ag(III)] t /dt = { kK 1 K 2 [OH - ][HOCH 2 CH 2 CH 2 CH 2 OH] 2 [Ag(III)] t }/{[H 2 IO 4 3- ] + K 1 [OH - ] + K 1 K 2 [OH - ][HOCH 2 CH 2 CH 2 CH 2 OH]} = k obs [Ag(III)] t . A plausible mechanism involving a pre-equilibrium of adduct formation between the complex and reductant was proposed. The activation parameters along with rate constants of the rate-determining step were calculated.

Key concepts: Kinetics, Chemistry, Adduct, Reaction rate constant, Medicinal chemistry, Rate equation, Nuclear chemistry, First order

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