摘要
A dual colorimetric and luminescent sensor based on a heteroleptic ruthenium dye [Ru（Hipdpa）（Hdcb- py）（NCS）2]^-.0.5H^＋ 0.5[N（C4H9）4]＋ Ru（Hipdpa） {where Hdcbpy = monodeprotonted-4,4＇-dicarboxy-2,2＇- bipyridine and Hipdpa = 4-（1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl）-N,N-diphenylaniline} for selective detection of Hg2. is presented. The results of spectrophotometric titrations revealed an evident luminescence intensity enhancement （I/Io = 11 ） and a considerable blue shift in visible absorption and luminescence maxima with the addition of rig2.. The sensitive response of the optical sensor on Hg^2＋ was attributed to the binding of the electron-deficient Hg^2＋ to the electron-rich sulfur atom of the thiocyanate （NCS） ligand in the Ru（Hipdpa）, which led to an increase in the energy gap between the highest occupied molecular orbital （HOMO） and the lowest unoccupied molecular orbital （LUMO）. Accordingly, the blue shift in the absorption spectrum of Ru（Hipdpa） due to the binding of Hg2. was obtained. Ru（Hipdpa） was found to have decreased Hg2~ detection limit and improved linear region as compared to di（tetrabutylammonium） cis-bis（isothiocyanato）bis（2,2＇-bipyridine-4-carboxylic acid-4＇- carboxylate）ruthenium（ll） N719. Moreover, a dramatic color change from pink to yellow was observed, which allowed simple monitoring of Hg^2＋ by either naked eyes or a simple colorimetric reader. Therefore, the proposed sensor can provide potential applications for Hg2＊ detection.
A dual colorimetric and luminescent sensor based on a heteroleptic ruthenium dye [Ru（Hipdpa）（Hdcb- py）（NCS）2]^-.0.5H^＋ 0.5[N（C4H9）4]＋ Ru（Hipdpa） {where Hdcbpy = monodeprotonted-4,4＇-dicarboxy-2,2＇- bipyridine and Hipdpa = 4-（1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl）-N,N-diphenylaniline} for selective detection of Hg2. is presented. The results of spectrophotometric titrations revealed an evident luminescence intensity enhancement （I/Io = 11 ） and a considerable blue shift in visible absorption and luminescence maxima with the addition of rig2.. The sensitive response of the optical sensor on Hg^2＋ was attributed to the binding of the electron-deficient Hg^2＋ to the electron-rich sulfur atom of the thiocyanate （NCS） ligand in the Ru（Hipdpa）, which led to an increase in the energy gap between the highest occupied molecular orbital （HOMO） and the lowest unoccupied molecular orbital （LUMO）. Accordingly, the blue shift in the absorption spectrum of Ru（Hipdpa） due to the binding of Hg2. was obtained. Ru（Hipdpa） was found to have decreased Hg2~ detection limit and improved linear region as compared to di（tetrabutylammonium） cis-bis（isothiocyanato）bis（2,2＇-bipyridine-4-carboxylic acid-4＇- carboxylate）ruthenium（ll） N719. Moreover, a dramatic color change from pink to yellow was observed, which allowed simple monitoring of Hg^2＋ by either naked eyes or a simple colorimetric reader. Therefore, the proposed sensor can provide potential applications for Hg2＊ detection.
基金
supports of the National Natural Science Foundation of China(Nos.21201037,21405019 and 21171022)
the Natural Science Foundation of Anhui Province(No. 1408085QB39)
the Innovation Training Program for the Anhui College students(Nos.AH201310371039 and AH201310371041)
Anhui Provincial Key Laboratory for Degradation and Monitoring of the Pollution of the Environment,and the Natural Science Foundation of Sichuan Provincial Department of Education(No. 13ZB0056)
Analytical and Measurements Fund of Beijing Normal University
