Takizawa Shinobu, Katayama Tomomi, Sasai Hiroaki
The Institute of Scientific and Industrial Research, Osaka University, Mihogaoka, Ibaraki-shi, Osaka 567-0047, Japan.
Chem Commun (Camb). 2008 Sep 21(35):4113-22. doi: 10.1039/b806016a. Epub 2008 Jul 17.
This review describes our recent efforts in the development of chiral dinuclear vanadium complexes that work as dual activation catalysts for the oxidative coupling of 2-naphthols. The dinuclear vanadium(iv) complex (R(a),S,S)- was prepared by complexation of VOSO(4) with the Schiff base derived from (R)-3,3'-diformyl-2,2'-dihydroxy-1,1'-binaphthyl () and (S)-tert-leucine. Since the dinuclear vanadium(iv) complex was found to be readily oxidized to afford a corresponding vanadium(v) species during preparation in air, a new synthetic procedure using VOCl(3) has been applied towards dinuclear vanadium(v) complexes (R(a),S,S)- and (R(a),S,S)-. To the best of our knowledge, (R(a),S,S)-, and show considerably higher catalytic activity than previously reported vanadium complexes for the oxidative coupling of 2-naphthols.
本综述描述了我们近期在开发手性双核钒配合物方面所做的努力,这些配合物可作为2-萘酚氧化偶联的双活化催化剂。双核钒(IV)配合物(R(a),S,S)-是通过将VOSO(4)与由(R)-3,3'-二甲酰基-2,2'-二羟基-1,1'-联萘()和(S)-叔亮氨酸衍生的席夫碱络合制备而成。由于发现双核钒(IV)配合物在空气中制备过程中容易被氧化生成相应的钒(V)物种,因此一种使用VOCl(3)的新合成方法已应用于双核钒(V)配合物(R(a),S,S)-和(R(a),S,S)-的制备。据我们所知,(R(a),S,S)-和在2-萘酚氧化偶联反应中表现出比先前报道的钒配合物高得多的催化活性。