An amphoteric reactivity of a mixed-valent bis(μ-oxo)dimanganese(III,IV) complex acting as an electrophile and a nucleophile

被引:24
作者
Sankaralingam, Muniyandi [1 ]
Jeon, So Hyun [1 ]
Lee, Yong-Min [1 ]
Seo, Mi Sook [1 ]
Ohkubo, Kei [1 ,2 ,3 ]
Fukuzumi, Shunichi [1 ,2 ,3 ,4 ,5 ]
Nam, Wonwoo [1 ]
机构
[1] Ewha Womans Univ, Dept Chem & Nano Sci, Seoul 120750, South Korea
[2] Osaka Univ, Grad Sch Engn, Dept Mat & Life Sci, ALCA, Suita, Osaka 5650871, Japan
[3] Japan Sci & Technol Agcy JST, SENTAN, Suita, Osaka 5650871, Japan
[4] Meijo Univ, Japan Sci & Technol Agcy JST, Fac Sci & Engn, ALCA, Nagoya, Aichi 4680073, Japan
[5] Meijo Univ, Japan Sci & Technol Agcy JST, SENTAN, Nagoya, Aichi 4680073, Japan
关键词
HYDROGEN-ATOM ABSTRACTION; EFFECTIVE CORE POTENTIALS; C-H; SPECTROSCOPIC CHARACTERIZATION; WATER OXIDATION; METAL-OXO; MOLECULAR CALCULATIONS; ENZYMATIC OXIDATION; MONONUCLEAR; PEROXO;
D O I
10.1039/c5dt04292e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A mixed-valent bis(mu-oxo)dimanganese(III,IV) complex, [(dpaq)Mn-III(O)(2)Mn-IV(dpaq)](+) (1), was prepared by reacting a hydroxomanganese(III) complex, [(dpaq)Mn-III(OH)](+), with hydrogen peroxide in the presence of triethylamine. The mixed-valent bis(mu-oxo)dimanganese(III,IV) complex (1) was well characterised by UV-vis, EPR and CSI-MS techniques. The electrophilic reactivity of 1 was investigated in the oxidation of 2,6-di- tert-butylphenol derivatives by 1, in which the relative rate afforded a good Hammett correlation with a rho value of -1.0. The nucleophilic character of 1 was then investigated in aldehyde deformylation reactions, using 2-phenylpropionaldehyde (2-PPA) and benzaldehyde derivatives as substrates. In contrast to the case of the reaction of 1 with 2,6-di-tert-butylphenol derivatives, a positive rho value of 0.89 was obtained in the Hammett plot, demonstrating that the bis(mu-oxo)-dimanganese(III,IV) complex is an active nucleophilic oxidant. Thus, 1 exhibited an amphoteric reactivity in both electrophilic and nucleophilic oxidative reactions.
引用
收藏
页码:376 / 383
页数:8
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