| Literature DB >> 25075382 |
Manjira Mukherjee1, Siddhartha Pal, Somenath Lohar, Buddhadeb Sen, Supriti Sen, Samya Banerjee, Snehasis Banerjee, Pabitra Chattopadhyay.
Abstract
A newly synthesized and crystalographically characterized napthelene–pyrazol conjugate, 1-[(5-phenyl-1H-pyrazole-3-ylimino)-methyl]-naphthalen-2-ol (HL) behaves as an Al(III) ion-selective chemosensor through internal charge transfer (ICT)-chelation-enhanced fluorescence (CHEF) processes in 100 mM HEPES buffer (water–DMSO 5:1, v/v) at biological pH with almost no interference of other competitive ions. This mechanism is readily studied from electronic, fluorimetric and (1)H NMR titration. The probe (HL) behaved as a highly selective fluorescent sensor for Al(III) ions as low as 31.78 nM within a very short response time (15–20 s). The sensor (HL), which has no cytotoxicity, is also efficient in detecting the distribution of Al(III) ions in HeLa cells via image development under fluorescence microscope.Entities:
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Year: 2014 PMID: 25075382 DOI: 10.1039/c4an01039f
Source DB: PubMed Journal: Analyst ISSN: 0003-2654 Impact factor: 4.616