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Push-pull conjugated chromene-derivatives for potential bio-imaging applications. Synthesis, X-Ray and DFT studies, one- and two-photon photophysical properties
被引:2
|作者:
Jin, Ying
[1
]
Chai, Zhiyong
[1
]
Rousselin, Yoann
[2
]
Pouzens, Jean-Thomas
[2
]
Fleurat-Lessard, Paul
[2
]
Gros, Claude P.
[2
]
Beau, Annaelle
[3
]
Bolze, Frederic
[3
]
Xu, Hai-Jun
[1
,4
]
机构:
[1] Nanjing Forestry Univ, Coll Chem Engn, Jiangsu Coinnovat Ctr Efficient Proc & Utilizat Fo, Nanjing 210037, Peoples R China
[2] Univ Bourgogne, ICMUB UMR CNRS 6302, F-21000 Dijon, France
[3] Univ Strasbourg, CNRS, Fac Pharm, Concept & Applicat Mol Bioact UMR 7199, 74 Route Rhin, F-67401 Illkirch Graffenstaden, France
[4] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453002, Peoples R China
关键词:
FLUORESCENT-PROBE;
RATIONAL DESIGN;
CHARGE-TRANSFER;
ABSORPTION;
DYES;
CHROMOPHORES;
TRANSITION;
EMISSION;
SPECTRA;
D O I:
10.1016/j.dyepig.2023.111866
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Dicyanomethylene-4H-benzopyran derivatives dyes containing D-pi-A-type structure have been prepared and fully characterized. The Z configuration of all three structures has been confirmed by SCXRD studies. Dyes 1-6 present a strong absorption in the 450-550 nm region with epsilon values over 43 000 M-1 cm-1 1-4 showed fluorescence properties while 5 and 6 are very weakly fluorescent. The electronic structure of the first singlet excited state S1 was investigated to further explain the evolution of fluorescence quantum yields. The two-photon excitation spectra were recorded with a similar behaviour upon two-photon excitation, with two ab-sorption bands, one in the 800-850 nm region with sigma 2 of 200-300 GM and another one at about 1000 nm with sigma 2 of 300-400 GM. Dyes 3 and 4 have shown interesting properties (both in intensity and FLIM modes) in two-photon excited microscopy.
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页数:9
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