中文版 | English
Title

Reactivity Studies of a Hydroxy-Substituted Irida-carbolong Complex

Author
Corresponding AuthorChen, Dafa; Xia, Haiping
Publication Years
2022-09-01
DOI
Source Title
ISSN
0276-7333
EISSN
1520-6041
Abstract
The reactivities of the aromatic beta-hydroxy-sub-stituted irida-carbolong complex [Ir{=CHC(CH2C-(CO2Me)(2)CH2)=CC=CHC(OH)=CH}(CO)(PPh3)(2)]BF4 (1) with a series of reagents, including AcCl, (CF3CO)(2)O, NaOH, Et2NSF3 and NaNO2/HBF4 center dot H2O, were studied, affording five new complexes [Ir{=CHC(CH2C(CO2Me)(2)CH2)=CC=CHC-(OCOCH3)=CH}(CO)(PPh3)(2)]BF4 (2), [Ir{=CHC(CH2C- (CO2Me)2CH(2))=CC=CHC(OCOCF3)=CH}(CO)(PPh3)(2)]-BF4 (3) , [Ir{CH=C(CH2C(CO2Me)(2)CH=)CC=CHC(O)-CH2}(CO)(PPh3)(2)] (4) , [Ir{=CHC(CH2C(CO2Me)(2)CH2)= CC=CHC(F)=CH}(CO)(PPh3)(2)]BF4 (5) , and [Ir{C(O)C- (CH2C(CO2Me)(2)CH2)=CC=CHC(O)CH=N(OH)}(NO2)-(PPh3)(2)] (6), in the yields of 61-87%, respectively. Each of complexes 2, 3 and 5 sti l l contains an iridapentalene fragment. In contrast, the [5,5]-fused iridabic y c l e in complex 4 is dearomatized, and the alteration of the metallabic y c l e skeleton was involved during the preparation of 6, with the transformation from a [5,5]-fused iridabicycle to a ring-expansion [5,6]-fused iridabicycle.
URL[Source Record]
Indexed By
Language
English
SUSTech Authorship
First ; Corresponding
Funding Project
National Natural Science Foundation of China["22071098","21871068","22101123","22101115"] ; Guangdong Provincial Key Laboratory of Catalysis[2020B121201002] ; Shenzhen Science and Technology Innovation Committee["JCYJ20200109140812302","JCYJ20210324105013035"]
WOS Research Area
Chemistry
WOS Subject
Chemistry, Inorganic & Nuclear ; Chemistry, Organic
WOS Accession No
WOS:000855906600001
Publisher
ESI Research Field
CHEMISTRY
Data Source
Web of Science
Citation statistics
Cited Times [WOS]:0
Document TypeJournal Article
Identifierhttp://kc.sustech.edu.cn/handle/2SGJ60CL/402379
DepartmentDepartment of Chemistry
深圳格拉布斯研究院
Affiliation
1.Southern Univ Sci & Technol, Dept Chem, Guangdong Prov Key Lab Catalysis, Shenzhen 518055, Peoples R China
2.Southern Univ Sci & Technol, Shenzhen Grubbs Inst, Shenzhen 518055, Peoples R China
3.Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, Xiamen 361005, Peoples R China
First Author AffilicationDepartment of Chemistry;  Shenzhen Grubbs Institute
Corresponding Author AffilicationDepartment of Chemistry;  Shenzhen Grubbs Institute
First Author's First AffilicationDepartment of Chemistry
Recommended Citation
GB/T 7714
Li, Jinhua,Chu, Zhenwei,Lu, Zhengyu,et al. Reactivity Studies of a Hydroxy-Substituted Irida-carbolong Complex[J]. ORGANOMETALLICS,2022.
APA
Li, Jinhua,Chu, Zhenwei,Lu, Zhengyu,Luo, Ming,Chen, Dafa,&Xia, Haiping.(2022).Reactivity Studies of a Hydroxy-Substituted Irida-carbolong Complex.ORGANOMETALLICS.
MLA
Li, Jinhua,et al."Reactivity Studies of a Hydroxy-Substituted Irida-carbolong Complex".ORGANOMETALLICS (2022).
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