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Mechanistic insights into the reactions of hydride transfer versus hydrogen atom transfer by a trans-dioxoruthenium(VI) complex
- Mechanistic insights into the reactions of hydride transfer versus hydrogen atom transfer by a trans-dioxoruthenium(VI) complex
- Dhuri, Sunder N.; Lee, Yong-Min; Seo, Mi Sook; Cho, Jaeheung; Narulkar, Dattaprasad D.; Fukuzumi, Shunichi; Nam, Wonwoo
- Ewha Authors
- 남원우; Shunichi Fukuzumi; 이용민; 서미숙; 조재흥
- SCOPUS Author ID
- 남원우; Shunichi Fukuzumi; 이용민; 서미숙
- Issue Date
- Journal Title
- DALTON TRANSACTIONS
- DALTON TRANSACTIONS vol. 44, no. 16, pp. 7634 - 7642
- ROYAL SOC CHEMISTRY
- SCI; SCIE; SCOPUS
- Document Type
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- A mononuclear high-valent trans-dioxoruthenium(VI) complex, trans-[Ru-VI(TMC)(O)(2)](2+) (TMC = 1,4,8,11-tetramethyl- 1,4,8,11-tetraazacyclotetradecane), was synthesized and characterized by various spectroscopic techniques and X-ray crystallography. The reactivity of the trans-[Ru-VI(TMC)(O)(2)](2+) complex was investigated in hydride transfer and hydrogen atom transfer reactions. The mechanism of hydride transfer from dihydronicotinamide adenine dinucleotide (NADH) analogues to trans-[Ru-VI(TMC)(O)(2)](2+), which proceeds via a proton-coupled electron transfer (PCET), followed by a rapid electron transfer (ET), has been proposed by the observation of a good linear correlation between the log rate constants of trans[ Ru-VI(TMC)(O)(2)](2+) and p-chloranil (Cl(4)Q) and a large kinetic isotope effect (KIE) value of 13(1). In the case of the oxidation of alkyl hydrocarbons by the trans-[Ru-VI(TMC)(O)(2)](2+) complex, the second-order rate constants were dependent on the C-H bond dissociation energy (BDE) of the substrates, and a large KIE value of 26(2) was obtained in the oxidation of xanthene and deuterated xanthene-d(2) by the trans[ RuVI(TMC)(O)(2)](2+) complex, indicating that the C-H bond activation of alkyl hydrocarbons proceeds via an H-atom abstraction in the rate-determining step.
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