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作 者:Jipan Yu Kang Liu Qunyan Wu Bin Li Xianghe Kong Kongqiu Hu Lei Mei Liyong Yuan Zhifang Chai Weiqun Shi
机构地区:[1]Laboratory of Nuclear Energy Chemistry,Institute of High Energy Physics,Chinese Academy of Sciences,Beijing 100049,China [2]Engineering Laboratory of Advanced Energy Materials,Institute of Industrial Technology,Chinese Academy of Sciences,Ningbo,Zhejiang 315201,China
出 处:《Chinese Journal of Chemistry》2021年第8期2125-2131,共7页中国化学(英文版)
基 金:This work was supported by the National Science Fund for Distinguished Young Scholars(No.21925603);the National Natural Science Foundation of China(No.21806167);the Science Challenge Project(TZ2016004);the Youth Inn ovation Promoti on Association of CAS(2017020).
摘 要:The issue of covale nee of acti nide complexes remai ns con troversial to date.The in troducti on of 2-phosphaethy nolate anion into acti・nide complexes is expected to in vestigate the reaction mode and the bon ding property.Herei n,we describe the function alizatio n of An(Tren^(TIPS))CI(1:An=U;2:An=Th)precursors with NaOCP(dioxane)_(2.5) through salt-elimination method leading to the formation of the corresponding uranium and thorium phosphaethynolate species:[U(Tren^(TIPS))(OCP)]⑶and[Th(Tren^(TIPS))(OCP)](4).
关 键 词:URANIUM THORIUM Tripodal ligand Computational chemistry Electronic structure
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