详细信息
PdCI2(Ph3P)2/Salicylaldimine Catalyzed Diarylation of Anilines with Unactivated Aryl Chlorides
文献类型:期刊文献
中文题名:PdCI2(Ph3P)2/Salicylaldimine Catalyzed Diarylation of Anilines with Unactivated Aryl Chlorides
英文题名:PdCI2(Ph3P)2/Salicylaldimine Catalyzed Diarylation of Anilines with Unactivated Aryl Chlorides
作者:Xiaochun Tao[1];Lei Li[1];Yu Zhou[2];Xuanying Qian[1];Min Zhao[1];Liangzhen Cai[1];Xiaomin Xie[2]
机构:[1]School of Chemistry and Molecular Engineering, East China University of Science and Technology, Shanghai 200237, China;[2]School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai 200240, China
年份:2017
卷号:35
期号:11
起止页码:1749
中文期刊名:Chinese Journal of Chemistry
外文期刊名:中国化学(英文版)
收录:CSTPCD;;Scopus;CSCD:【CSCD2017_2018】;
基金:We thank the National Natural Science Foundationof China (21272156) for financial support.
语种:英文
中文关键词:palladium;diarylation;aryl chloride;triphenylphosphine;salicyaldimine
外文关键词:palladium, diarylation, aryl chloride, triphenylphosphine, salicyaldimine
摘要:Triphenylphosphine and salicylaldimine could be used as a mixed ligand system to obtain a high catalytic activ- ity for palladium catalyzed diarylation of primary anilines with unactivated aryl chlorides by the synergistic effect of ligands. The activity and selectivity of the catalytic system could be improved by modifying the structure of sa- licylaldimine. In refluxing o-xylene, PdC12(Ph3P)2 with 2,5-ditrifluoromethyl N-phenylsalicylaldimine as a coligand shows high efficiency for the diarylation of various anilines. The catalytic system shows good toleration for the ste- ric hindrance of the substrates. The facile catalytic system works as well on the multiple arylation of 1, 1'-biphenyl- 4,4'-diamine with aryl chlorides to afford N,N,N'y'-tetraaryl-1,1'-biphenyl-4,4'-diamines which are important in- termediates of organic light emitting diode (OLED) hole transport materials.
Triphenylphosphine and salicylaldimine could be used as a mixed ligand system to obtain a high catalytic activ- ity for palladium catalyzed diarylation of primary anilines with unactivated aryl chlorides by the synergistic effect of ligands. The activity and selectivity of the catalytic system could be improved by modifying the structure of sa- licylaldimine. In refluxing o-xylene, PdC12(Ph3P)2 with 2,5-ditrifluoromethyl N-phenylsalicylaldimine as a coligand shows high efficiency for the diarylation of various anilines. The catalytic system shows good toleration for the ste- ric hindrance of the substrates. The facile catalytic system works as well on the multiple arylation of 1, 1'-biphenyl- 4,4'-diamine with aryl chlorides to afford N,N,N'y'-tetraaryl-1,1'-biphenyl-4,4'-diamines which are important in- termediates of organic light emitting diode (OLED) hole transport materials.
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