Organocopper(III) Compounds with Well-defined Structures Undergo Reductive Elimination to Form C-C or C-Heteroatom Bonds
文献类型:期刊论文
作者 | Liu, Liang; Xi, Zhenfeng |
刊名 | CHINESE JOURNAL OF CHEMISTRY
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出版日期 | 2018-12-01 |
卷号 | 36期号:12页码:1213-1221 |
关键词 | structure elucidation copper reactive intermediate organocopper(III) organocuprate(III) reductive elimination |
ISSN号 | 1001-604X |
DOI | 10.1002/cjoc.201800365 |
通讯作者 | Liu, Liang(liang.liu@pku.edu.cn) ; Xi, Zhenfeng(zfxi@pku.edu.cn) |
英文摘要 | Reductive elimination around Cu(III) atom arises an increasing attention, since this organometallic pathway has been often proposed in a range of Cu-based reactions. However, due to limited organocopper(III) compounds with well-defined structures, this elementary reaction still remains an extremely challenging issue. In this review, structurally well-defined organocopper(III) compounds are mainly divided into three classes based on their ligands: perfluoromethyl Cu(III) compounds, macrocyclic ligand-based aryl-Cu(III) compounds, and spiro organocopper(III) compounds chelated by bidentate ligands. The majority of organocopper(III) compounds display the typical square planar geometry. There also exist a few penta-coordinated organocopper(III) complexes, which share a weak apical Cu-L bond. In order to form a cis Cu(III)-C and Cu(III)-Nu bonding geometry required for reductive elimination, the re-arrangement of coordination modes around tetra-coordinated Cu(III) atoms is necessary. For the aryl-Cu(III) cationic complexes with one Cu(III)-C bond, the re-arrangement is triggered by the coordination of the fifth ligand (solvent or nucleophiles), while for the tetra-carbon-coordinated organocuprate(III) compounds, the process might be realized via the cleavage of one Cu(III)-C bond by attack of electrophiles. Stoichiometric and catalytic reactions involving well-defined organocopper(III) compounds to form C-C or C-heteroatom bonds are discussed to support their intermediacy. |
WOS关键词 | TRANSITION-METAL-COMPLEXES ; CROSS-COUPLING REACTIONS ; N-CONFUSED PORPHYRINS ; RAPID INJECTION NMR ; X-RAY-STRUCTURE ; H BOND ; TRIFLUOROMETHYL COMPLEXES ; CONJUGATE ADDITION ; CATALYTIC CYCLE ; COPPER(III) INTERMEDIATE |
资助项目 | National Natural Science Foundation of China[21690061] |
WOS研究方向 | Chemistry |
语种 | 英语 |
WOS记录号 | WOS:000450017200020 |
出版者 | WILEY-V C H VERLAG GMBH |
资助机构 | National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China |
源URL | [http://cas-ir.dicp.ac.cn/handle/321008/166688] ![]() |
专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
通讯作者 | Liu, Liang; Xi, Zhenfeng |
作者单位 | Peking Univ, Key Lab Bioorgan Chem & Mol Engn, BNLMS, Minist Educ,Coll Chem, Beijing 100871, Peoples R China |
推荐引用方式 GB/T 7714 | Liu, Liang,Xi, Zhenfeng. Organocopper(III) Compounds with Well-defined Structures Undergo Reductive Elimination to Form C-C or C-Heteroatom Bonds[J]. CHINESE JOURNAL OF CHEMISTRY,2018,36(12):1213-1221. |
APA | Liu, Liang,&Xi, Zhenfeng.(2018).Organocopper(III) Compounds with Well-defined Structures Undergo Reductive Elimination to Form C-C or C-Heteroatom Bonds.CHINESE JOURNAL OF CHEMISTRY,36(12),1213-1221. |
MLA | Liu, Liang,et al."Organocopper(III) Compounds with Well-defined Structures Undergo Reductive Elimination to Form C-C or C-Heteroatom Bonds".CHINESE JOURNAL OF CHEMISTRY 36.12(2018):1213-1221. |
入库方式: OAI收割
来源:大连化学物理研究所
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