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Cu(II) complex-based fluorescence chemosensor for cyanide in aqueous media  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Cu(II) complex-based fluorescence chemosensor for cyanide in aqueous media

作者:Wang, Dan[1];Zheng, Jian-Quan[1,2];Yan, Xi[1];Zheng, Xiang-Jun[1];Jin, Lin-Pei[1]

第一作者:Wang, Dan

通讯作者:Zheng, XJ[1]

机构:[1]Beijing Normal Univ, Coll Chem, Beijing Key Lab Energy Convers & Storage Mat, Beijing 100875, Peoples R China;[2]Beijing Union Univ, Beijing Key Lab Bioact Subst & Funct Foods, Beijing 100191, Peoples R China

第一机构:Beijing Normal Univ, Coll Chem, Beijing Key Lab Energy Convers & Storage Mat, Beijing 100875, Peoples R China

通讯机构:[1]corresponding author), Beijing Normal Univ, Coll Chem, Beijing Key Lab Energy Convers & Storage Mat, Beijing 100875, Peoples R China.

年份:2015

卷号:5

期号:79

起止页码:64756-64762

外文期刊名:RSC ADVANCES

收录:;EI(收录号:20153201114029);Scopus(收录号:2-s2.0-84938567056);WOS:【SCI-EXPANDED(收录号:WOS:000358786400090)】;

基金:This study is supported by the National Natural Science Foundation of China (20971015) and the Fundamental Research Funds for the Central Universities.

语种:英文

外文关键词:Crystal structure - Fluorescence

摘要:A fluorescent quinazoline derivative, 6-(2,4-dihydroxyphenyl)-5,6-dihydrobenzoimidazo[1,2-c]quinazoline (H2L), was designed and synthesized. Its fluorescence could be quenched by the addition of Cu2+ in an aqueous media. The binding constant for Cu2+ and H2L was determined to be 9.56 x 10(3) M-2 in DMSO/H2O (1 : 1, v/v). The crystal structure of the Cu(II) complex, [Cu(HL1)(Ac)] (1) (H2L1 = 4-{[2-(1H-benzimidazol-2-yl)-phenylimino]-methyl}-benzene-1,3-diol, Ac = acetate), revealed that Schiff base complex 1, H2L1, was formed in the response system of H2L to Cu2+ via Cu2+-assisted C-N bond breakage of the quinazoline ring in H2L. Consequently, complex 1 was used as a turn-on fluorescence chemosensor for the direct detection of CN-, and showed a high selectivity to CN- over a number of anions in the aqueous media, where CN- replaces HL1 in 1 to form [Cu(CN)(x)](2-x) with HL1 then released and the fluorescence recovered. The detection limit for CN- was 4.0 x 10(-6) M. The cell images showed that 1 could be used to detect intracellular CN-.

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