Asgari Parham, Hua Yuanda, Bokka Apparao, Thiamsiri Chanachon, Prasitwatcharakorn Watcharapon, Karedath Ashif, Chen Xin, Sardar Sinjinee, Yum Kyungsuk, Leem Gyu, Pierce Brad S, Nam Kwangho, Gao Jiali, Jeon Junha
Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, Texas 76019, USA.
Department of Chemistry, Mahidol University, Bangkok, 10400, Thailand.
Nat Catal. 2019 Feb;2:164-173. doi: 10.1038/s41929-018-0217-z. Epub 2019 Jan 28.
Because of the importance of hydrogen atom transfer (HAT) in biology and chemistry, there is increased interest in new strategies to perform HAT in a sustainable manner. Here, we describe a sustainable, net redox-neutral HAT process involving hydrosilanes and alkali metal Lewis base catalysts - eliminating the use of transition metal catalysts - and report an associated mechanism concerning Lewis base-catalysed, complexation-induced HAT (LBCI-HAT). The catalytic LBCI-HAT is capable of accessing both branch-specific hydrosilylation and polymerization of vinylarenes in a highly selective fashion, depending on the Lewis base catalyst used. In this process, earth abundant, alkali metal Lewis base catalyst plays a dual role. It first serves as a HAT initiator and subsequently functions as a silyl radical stabilizing group, which is critical to highly selective cross-radical coupling. EPR study identified a potassiated paramagnetic species and multistate density function theory revealed a high HAT character, yet multiconfigurational nature in the transition state of the reaction.
由于氢原子转移(HAT)在生物学和化学中的重要性,人们对以可持续方式进行HAT的新策略越来越感兴趣。在此,我们描述了一种可持续的、净氧化还原中性的HAT过程,该过程涉及硅烷和碱金属路易斯碱催化剂——无需使用过渡金属催化剂——并报告了一种关于路易斯碱催化的、络合诱导的HAT(LBCI-HAT)的相关机制。催化性的LBCI-HAT能够根据所使用的路易斯碱催化剂,以高度选择性的方式实现乙烯基芳烃的支链特异性硅氢化和聚合。在这个过程中,储量丰富的碱金属路易斯碱催化剂发挥了双重作用。它首先作为HAT引发剂,随后作为硅基自由基稳定基团,这对高度选择性的交叉自由基偶联至关重要。电子顺磁共振研究确定了一种钾化顺磁物种,多态密度泛函理论揭示了反应过渡态中较高的HAT特征以及多构型性质。