检索结果-南通市图书馆

Imidodiphosphorimidates (IDPis): catalyst Motifs with Unprecedented Reactivity and Selectivity

Chinese Journal of Chemistry 2023年第6期41卷 685-694页

作者： Jun Kee Cheng Shao-Hua Xiang Bin Tan Shenzhen Grubbs Institute and Department of Chemistry Guangdong Provincial Key Laboratory of CatalysisSouthern University of Science and TechnologyShenzhenGuangdong 518055China Academy for Advanced Interdisciplinary Studies Southern University of Science and TechnologyShenzhenGuangdong 518055China

The conceptually designed imidodiphosphorimidates(IDPis)have emerged as one of the most potent classes of chiral acid catalysts.They are characterized by enzyme-like,highly confined active site and high acidity,which underlie their wide-reaching applications as Bronsted acid catalysts and as precatalysts for silylium lewis acids.Many carbon-carbon and carbon-heteroatom bond formation reactions that were deemed intractable could now be attained with spectacular reactivity and selectivity.Substrates that are small,unbiased and/or possess insufficient reactivity such as simple alkenes could now be engaged.The high structural confinement is particularly invaluable to control stereo-and chemoselectivity.The well-defined steric environment offers unique opportunity to control high-energy but structurally unbiased cation intermediates such as the norbonyl cations.Beyond practical appeals such as good scalability as well as ease and modularity of preparation,the extremely low pre-catalyst loadings required to achieve high turnover and stereoselectivity have also come to define a new frontier in organocatalysis.

关键词： Bronsted acid catalyst lewis acid catalyst Silylium ACDC Imidodiphosphorimidates Asymmetric organocatalysis

来源：

维普期刊数据库评论

在线全文

维普期刊数据库

学校读者我要写书评

暂无评论

Four novel Z-shaped hexanuclear vanadium oxide clusters as efficient heterogeneous catalysts for cycloaddition of CO_(2) and oxidative desulfurization reactions

引用

Chinese Chemical Letters 2023年第1期34卷 478-482页

作者： Jilei Wang Jiapeng Cao Zeyu Du Xiaomei Liu Jianian Li Qingdong Ping Tingting Zang Yan Xu College of Chemical Engineering State Key Laboratory of Materials-Oriented Chemical EngineeringNanjing Tech UniversityNanjing 211800China Coordination Chemistry Institute State Key Laboratory of Coordination ChemistryNanjing UniversityNanjing 210093China

Chemical fixation of CO_(2)into C1 source, as a general approach, can effectively alleviate the emission of greenhouse gasses. Whereas, the challenge posed by the need for efficient catalysts with high catalytic active sites still exists. In this work, we reported a series of new hexavanadate clusters, [(C6H6ON)2(C2H8N2)2(CH3O)6VIV6O8](V6–1), [(C6H6ON)2(C3H10N2)2(CH3O)6VIV6O8](V6–2), [(C6H6ON)2(C6H14N2)2(CH3O)6VIV6O8](V6–3) and [(C6H6ON)2(C4H11N2O)2(CH3O)4VIV6O8](V6–4), assembled by 2-aminophenol and four different kinds of lewis bases(LB), ethanediamine(en), 1,2-diaminopropane, 1,2-cyclohexanediamine and N-(2-hydroxyethyl)ethylenediamine(ben) together. Among them, the basic unit {V6} cluster featured Z-shaped configuration represents a brand-new example of hexanuclear vanadium clusters. Remarkably, the catalytic tests demonstrated that V6–1 as catalyst displays high catalytic activity in the cycloaddition for the CO_(2)fixation into cyclic carbonates by virtue of open V sites. As expected, for oxidative desulfurization of sulfides, V6–1 also exhibits satisfied catalytic effectiveness. Furthermore, the recycling test confirmed that catalyst V6–1 may be a bifunctional heterogeneous catalyst with great promise for both CO_(2)cycloaddition and oxidative desulfurization reactions.

关键词： Z-shaped Hexavanadate cluster lewis acid catalyst Cycloaddition of CO_(2) Oxidative desulfurization

来源：

维普期刊数据库

同方期刊数据库评论

在线全文

学校读者我要写书评

暂无评论

欢迎您,

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案：

请选择收藏分类：

通借通还

欢迎您,

建议与咨询 留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

时间限定

文献类型

馆藏选择

核心期刊

语言

文献类型

帮助

文字说明：

检索规则说明：

检索范例：

分类表

所选分类

限定检索结果

文献类型

馆藏范围

日期分布

学科分类号

主题

机构

作者

语言

在线全文

在线全文

请选择保存的检索档案： 新增检索档案 确定 取消

请选择收藏分类： 新增自定义分类 确定 取消

通借通还

建议与咨询留下您的常用邮箱和电话号码，以便我们向您反馈解决方案和替代方法

请选择保存的检索档案：

请选择收藏分类：