期刊
CHEMICAL COMMUNICATIONS
卷 48, 期 7, 页码 1039-1041出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c1cc16064h
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资金
- JNCASR
- DST
- CSIR
A novel quinoline-coumarin (QC) fluoroionophore conjugated by means of a triazolyl-pyrrolidinyl linker exhibits differential dual selectivity for Zn2+ and Al3+ in mixed media. QC acts as a turn on fluorescence sensor for Zn2+ while exhibiting overall ratiometric selectivity for Al3+ in aqueous media. Moreover, QC exhibited preferential second mode of selectivity for Al3+ as it ratiometrically displaces Zn2+ from the [QC + Zn2+] complex.
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