GIEC OpenIR  > 中国科学院广州能源研究所
A Schiff base-modified silver catalyst for efficient fixation of CO2 as carboxylic acid at ambient pressure
Wu, Zhilian1,2,3; Sun, Lei2; Liu, Qinggang2,4; Yang, Xiaofeng2; Ye, Xue2; Hu, Yancheng2; Huang, Yanqiang2
2017-05-07
发表期刊GREEN CHEMISTRY
卷号19期号:9页码:2080-2085
摘要The fixation of CO2 as a carboxylic acid is a significant reaction for C-C bond formation in organic synthesis. So far, besides C-H carboxylations using stoichiometric amounts of metals or organometallic reagents, great efforts have been devoted to develop new heterogeneous catalyst, while the catalytic performance of supported metal catalysts is not satisfactory. Herein, a Schiff basemodified silver catalyst was developed for the direct carboxylation of terminal alkynes with CO2, enabling an efficient and green synthesis of valuable alkynyl carboxylic acids. The reaction can smoothly proceed under atmospheric pressure and low temperature (60 degrees C) conditions. Moreover, a silver-based catalyst, which was prepared by an in situ reduction route, can be easily prepared, recovered, and reused five times without significant loss of activity due to the stability promoted by the Schiff-base on the support surface. In addition, the markedly negative influence of H2O and solvent effect on this reaction system has also been discussed.
文章类型Article
WOS标题词Science & Technology ; Physical Sciences
资助者National Natural Science Foundation of China(21403218 ; China Ministry of Science and Technology(2016YFB0600902) ; Dalian Science Foundation for Distinguished Young Scholars(2016RJ04) ; Youth Innovation Promotion Association CAS ; 21476226 ; 21503125 ; 21506204) ; National Natural Science Foundation of China(21403218 ; China Ministry of Science and Technology(2016YFB0600902) ; Dalian Science Foundation for Distinguished Young Scholars(2016RJ04) ; Youth Innovation Promotion Association CAS ; 21476226 ; 21503125 ; 21506204)
DOI10.1039/c7gc00923b
研究领域[WOS]Chemistry
关键词[WOS]CARBON-DIOXIDE ; TERMINAL ALKYNES ; ORGANIC-SYNTHESIS ; WATER ; NANOPARTICLES ; CONVERSION ; GREEN ; CU ; HYDROGENATION ; CHEMISTRY
收录类别SCI
语种英语
资助者National Natural Science Foundation of China(21403218 ; China Ministry of Science and Technology(2016YFB0600902) ; Dalian Science Foundation for Distinguished Young Scholars(2016RJ04) ; Youth Innovation Promotion Association CAS ; 21476226 ; 21503125 ; 21506204) ; National Natural Science Foundation of China(21403218 ; China Ministry of Science and Technology(2016YFB0600902) ; Dalian Science Foundation for Distinguished Young Scholars(2016RJ04) ; Youth Innovation Promotion Association CAS ; 21476226 ; 21503125 ; 21506204)
WOS类目Chemistry, Multidisciplinary
WOS记录号WOS:000400836500004
引用统计
被引频次:9[WOS]   [WOS记录]     [WOS相关记录]
文献类型期刊论文
条目标识符http://ir.giec.ac.cn/handle/344007/14169
专题中国科学院广州能源研究所
作者单位1.Chinese Acad Sci, CAS Key Lab Renewable Energy, Guangzhou Inst Energy Convers, Guangzhou 510640, Guangdong, Peoples R China
2.Chinese Acad Sci, State Key Lab Catalysis, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
3.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
4.Dalian Univ Technol, Sch Chem, Lab Adv Mat & Catalyt Engn, Dalian 116024, Peoples R China
推荐引用方式
GB/T 7714
Wu, Zhilian,Sun, Lei,Liu, Qinggang,et al. A Schiff base-modified silver catalyst for efficient fixation of CO2 as carboxylic acid at ambient pressure[J]. GREEN CHEMISTRY,2017,19(9):2080-2085.
APA Wu, Zhilian.,Sun, Lei.,Liu, Qinggang.,Yang, Xiaofeng.,Ye, Xue.,...&Huang, Yanqiang.(2017).A Schiff base-modified silver catalyst for efficient fixation of CO2 as carboxylic acid at ambient pressure.GREEN CHEMISTRY,19(9),2080-2085.
MLA Wu, Zhilian,et al."A Schiff base-modified silver catalyst for efficient fixation of CO2 as carboxylic acid at ambient pressure".GREEN CHEMISTRY 19.9(2017):2080-2085.
条目包含的文件
条目无相关文件。
个性服务
推荐该条目
保存到收藏夹
查看访问统计
导出为Endnote文件
谷歌学术
谷歌学术中相似的文章
[Wu, Zhilian]的文章
[Sun, Lei]的文章
[Liu, Qinggang]的文章
百度学术
百度学术中相似的文章
[Wu, Zhilian]的文章
[Sun, Lei]的文章
[Liu, Qinggang]的文章
必应学术
必应学术中相似的文章
[Wu, Zhilian]的文章
[Sun, Lei]的文章
[Liu, Qinggang]的文章
相关权益政策
暂无数据
收藏/分享
所有评论 (0)
暂无评论
 

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。