On/Off Fluorescent Chemosensor for Selective Detection of Divalent Iron and Copper Ions: Molecular Logic Operation and Protein Binding
Author(s) -
G. Tamil Selvan,
Chitra Varadaraju,
Ramadoss Tamil Selvan,
Israel V.M.V. Enoch,
P. Mosae Selvakumar
Publication year - 2018
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.8b00748
Subject(s) - chemistry , divalent , fluorescence , quenching (fluorescence) , binding constant , förster resonance energy transfer , ion , stoichiometry , copper , photochemistry , inorganic chemistry , binding site , organic chemistry , biochemistry , physics , quantum mechanics
Here, naphthalene diamine-based β-diketone derivative (compound LH) was successfully used as a dual signaling probe for divalent cations, Fe 2+ and Cu 2+ ions, in bimodal methods (colorimetric and fluorometric). It showed fluorescent enhancement for Fe 2+ ion by photoinduced electron transfer mechanism and fluorescence quenching for Cu 2+ ion by charge-transfer process. Binding stoichiometry for [LH-(Fe 2+ ) 2 ] and [LH-(Cu 2+ ) 2 ] was found to be 1:2 by Job's plot method and, the binding constants were calculated as 1.6638 × 10 10 and 9.22929 × 10 8 M -1 , respectively. Compound LH exhibited OR and XOR logic gate behavior with H + , Fe 2+ , and Cu 2+ as inputs. Further, the compound LH and bovine serum albumin binding interaction showed quenching of fluorescence by Förster resonance energy-transfer mechanism.
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