Dehydrogenation and Related Reactions Catalyzed by Iridium Pincer Complexes

被引:892
作者
Choi, Jongwook [2 ]
MacArthur, Amy H. Roy [1 ]
Brookhart, Maurice [3 ]
Goldman, Alan S. [2 ]
机构
[1] USN Acad, Dept Chem, Annapolis, MD 21402 USA
[2] Rutgers State Univ, Dept Chem & Chem Biol, New Brunswick, NJ 08903 USA
[3] Univ N Carolina, Dept Chem, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
C-H BONDS; AMINE-BORANE ADDUCTS; METAL-CARBON BONDS; (PCP)IR-CATALYZED ACCEPTORLESS DEHYDROGENATION; THERMOCHEMICAL ALKANE DEHYDROGENATION; X-RAY-STRUCTURE; TRANSITION-METAL; PCP-PINCER; AMMONIA-BORANE; LARGE-RING;
D O I
10.1021/cr1003503
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Studies conducted in the field of dehydrogenation and related reactions catalyzed by iridium pincer complexes are compiled. Koridze et al. reported that ferrocene and ruthenocene-based iridium pincer complexes showing excellent catalytic activity for COA/TBE transfer dehydrogenation. In 2006, Goldman, Brookhart, and co-workers reported alkane metathesis by tandem alkane dehydrogenation and olefin metathesis using combinations of an iridium pincer complex and the Schrock catalyst. Kaska and Jensen reported the dehydrogenation of ethylbenzene and tetrahydrofuran and proposed that interaction between the catalyst and arene or oxygen groups inhibited the catalysis. In 2006, ammonia-borane dehydrogenation by a well-defined molecular complex was reported by Goldberg and Heinekey, and it was considered that alkane dehydrogenation catalysts might also effect the dehydrogenation of ammonia-borane.
引用
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页码:1761 / 1779
页数:19
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