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Activation of C−F Bonds by Electrophilic Organosilicon Sites Supported on Sulfated Zirconia
Angewandte Chemie International Edition ( IF 16.6 ) Pub Date : 2018-10-15 , DOI: 10.1002/anie.201809199
Damien B. Culver 1 , Matthew P. Conley 1
Affiliation  

The reaction of allyltriisopropylsilane with partially dehydroxylated sulfated zirconium oxide (SZO) forms surface organosilicon species. Solid‐state NMR studies of the organosilicon functionalized SZO shows that electrophilic [TIPS][SZO] sites are present on the surface, in addition to less reactive TIPS‐Ox and SiOx species. The electrophilic [TIPS][SZO] sites are strong Lewis acids from solid‐state 31P NMR analysis of triethylphosphine oxide (O=PEt3) contacted materials. [TIPS][SZO] is active in hydrodefluorination reactions in the presence of Et3SiH.

中文翻译:

硫酸化氧化锆上支持的亲电子有机硅位点活化C-F键

烯丙基三异丙基硅烷与部分脱羟基的硫酸氧化锆(SZO)反应形成表面有机硅物质。对有机硅官能化的SZO进行的固态NMR研究表明,表面上存在亲电[TIPS] [ SZO ]部位,除了反应性较差的TIPS-O x和SiO x种类之外。亲电子的[TIPS] [ SZO ]位是强三氧化二膦(O = PEt 3)接触材料的固态31 P NMR分析得到的强路易斯酸。[TIPS] [ SZO ]在Et 3 SiH存在下的加氢氟化反应中具有活性。
更新日期:2018-10-15
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