Specific Enhancement of Catalytic Activity by a Dicopper Core: Selective Hydroxylation of Benzene to Phenol with Hydrogen Peroxide

被引:78
作者
Tsuji, Tomokazu [1 ]
Zaoputra, Antonius Andre [1 ]
Hitomi, Yutaka [1 ]
Mieda, Kaoru [2 ]
Ogura, Takashi [2 ]
Shiota, Yoshihito [3 ]
Yoshizawa, Kazunari [3 ]
Sato, Hiroyasu [4 ]
Kodera, Masahito [1 ]
机构
[1] Doshisha Univ, Dept Mol Chem & Biochem, Kyoto 6100321, Japan
[2] Univ Hyogo, Dept Life Sci, Kouto 2-1, Kamigori, Hyogo 6781297, Japan
[3] Kyushu Univ, Inst Mat Chem & Engn, Fukuoka 8190395, Japan
[4] Rigaku Corp, Applicat Lab, Akishima, Tokyo 1968666, Japan
关键词
arenes; copper; oxidation; reaction mechanisms; structure elucidation; MESOPOROUS SILICA-ALUMINA; ROOM-TEMPERATURE; MU-ETA(2)-ETA(2)-PEROXODICOPPER(II) COMPLEX; CRYSTAL-STRUCTURE; OXIDATION; REACTIVITY; BINDING; MEMBRANE; REAGENT; METHANE;
D O I
10.1002/anie.201702291
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A dicopper(II) complex, stabilized by the bis(tpa)ligand 1,2-bis[2-[bis(2-pyridylmethyl)aminomethyl]-6-pyridyl]ethane (6-hpa), [Cu-2(mu-OH)(6-hpa)](3+), was synthesized and structurally characterized. This complex catalyzed selective hydroxylation of benzene to phenol using H2O2, thus attaining large turnover numbers (TONs) and high H2O2 efficiency. The TON after 40 hours for the phenol production exceeded 12000 in MeCN at 50 degrees C under N-2, the highest value reported for benzene hydroxylation with H2O2 catalyzed by homogeneous complexes. At 22% benzene conversion, phenol (95.2%) and p-benzoquinone (4.8%) were produced. The mechanism of H2O2 activation and benzene hydroxylation is proposed.
引用
收藏
页码:7779 / 7782
页数:4
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