Radical Reactions of Silanes
Radical Reactions of Silanes
复制标题
硅烷的自由基反应
DOI:
10.1007/978-1-4613-3427-9_3
复制
发表时间:
1983
期刊:
影响因子:
--
通讯作者:
J. Wilt
中科院分区:
文献类型:
--
作者:
J. Wilt
Silicon, after oxygen the most abundant element in the earth's crust (28% by weight), has deservedly an equally abundant chemistry. 1 Although obscured somewhat by the shadow of its congener carbon and its overwhelming array of transformations, the chemistry of silicon has been an ever-increasing area of importance. Two astounding reactions, the" direct synthesis" of halosilanes (1945) 2 and the transition-metal-complex-catalyzed" hydrosilylation" process (1957)/opened the door to organosilicon chemistry especially, even though the subject dates back considerably prior to them both. 4 Direct synthesis made the silicones5 commercially available, and one need not elaborate on the significance of that achievement. Hydrosilylation made thousands of new organosilanes available, 6 which in turn led exponentially to their further exploitation.Clearly, from such an abundance of information available, one must necessarily be selective in a review chapter. The task at hand is the radical reactions of silanes, a rather small fraction of the total wealth residing in organosilicon chemistry and indeed a fraction missing both the direct synthesis and the major type of hydrosilylation. Yet even here advances continue to be made which indicate the versatility of silicon in this type of process. Excellent earlier compilations 7-9 of such reactions behoove one to do a careful job of citing the important earlier work contained in these reviews as well as new findings.