石油化工
烷烃
利用
金属有机化学
催化作用
化学
惰性
生化工程
第2组金属有机化学
纳米技术
债券
组合化学
计算机科学
材料科学
分子
有机化学
业务
工程类
财务
计算机安全
作者
Jay A. Labinger,John E. Bercaw
出处
期刊:Nature
[Nature Portfolio]
日期:2002-05-01
卷期号:417 (6888): 507-514
被引量:2619
摘要
The selective transformation of ubiquitous but inert C–H bonds to other functional groups has far-reaching practical implications, ranging from more efficient strategies for fine chemical synthesis to the replacement of current petrochemical feedstocks by less expensive and more readily available alkanes. The past twenty years have seen many examples of C–H bond activation at transition-metal centres, often under remarkably mild conditions and with high selectivity. Although profitable practical applications have not yet been developed, our understanding of how these organometallic reactions occur, and what their inherent advantages and limitations for practical alkane conversion are, has progressed considerably. In fact, the recent development of promising catalytic systems highlights the potential of organometallic chemistry for useful C–H bond activation strategies that will ultimately allow us to exploit Earth's alkane resources more efficiently and cleanly.
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