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Nuclearity effects in supported, single-site Fe(ii) hydrogenation pre-catalysts†‡
Dalton Transactions ( IF 3.5 ) Pub Date : 2018-07-17 00:00:00 , DOI: 10.1039/c8dt02720j
Ryan R. Langeslay 1, 2, 3, 4 , Hyuntae Sohn 1, 2, 3, 4 , Bo Hu 1, 2, 3, 4, 5 , Jacob S. Mohar 1, 2, 3, 4 , Magali Ferrandon 1, 2, 3, 4 , Cong Liu 1, 2, 3, 4 , Hacksung Kim 1, 2, 3, 4, 6 , A. Jeremy Kropf 1, 2, 3, 4 , Ce Yang 1, 2, 3, 4 , Jens Niklas 1, 2, 3, 4 , Oleg G. Poluektov 1, 2, 3, 4 , E. Ercan Alp 2, 3, 4, 7 , Patricia Ignacio-de Leon 2, 3, 4, 8 , Alfred P. Sattelberger 1, 2, 3, 4 , Adam S. Hock 1, 2, 3, 4, 5 , Massimiliano Delferro 1, 2, 3, 4
Affiliation  

Dimeric and monomeric supported single-site Fe(II) pre-catalysts on SiO2 have been prepared via organometallic grafting and characterized with advanced spectroscopic techniques. Manipulation of the surface hydroxyl concentration on the support influences monomer/dimer formation. While both pre-catalysts are highly active in liquid-phase hydrogenation, the dimeric pre-catalyst is ∼3× faster than the monomer. Preliminary XAS experiments on the H2-activated samples suggest the active species are isolated Fe(II) sites.

中文翻译:

负载型单中心Fe(ii)加氢预催化剂中的核效应

SiO 2上的聚和单体负载单中心Fe(II)预催化剂已通过有机金属接枝制备并通过先进的光谱技术进行了表征。载体上表面羟基浓度的控制影响单体/二聚体的形成。尽管两种预催化剂在液相加氢中均具有很高的活性,但二聚体预催化剂比单体快约3倍。对H 2活化的样品进行的初步XAS实验表明,活性物种是分离的Fe(II)位点。
更新日期:2018-07-17
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