Photophysical parameters and laser performance of 3-(4′-dimethylaminophenyl)-1-(2-furanyl)prop-2-en-1-one (DMAFP): A new laser dye

被引:14
作者
El-Daly, S. A. [1 ]
Gaber, M. [1 ]
El-Sayed, Y. S. [1 ]
机构
[1] Tanta Univ, Fac Sci, Dept Chem, Tanta 31527, Egypt
关键词
Fluorescence quantum yield and photostability; Solvent effect; Laser dye; INTRAMOLECULAR CHARGE-TRANSFER; PHOTOCHEMICAL-REACTION; CHALCONE-ANALOG; BETA-CARBOLINES; EXCITED-STATES; QUANTUM YIELDS; FLUORESCENCE; MEDIA; LIGHT; ACID;
D O I
10.1016/j.optlastec.2009.01.005
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The spectral properties such as singlet absorption, molar absorptivity, emission spectra, fluorescence quantum yield and excited state lifetime of 3-(4'-dimethylaminophenyl)-1-(2-furanyl)prop-2-en-1-one (DMAFP) have been determined in different solvents. DMAFP dye exhibits a large red shift in both electronic absorption and emission spectra as the solvent polarity increases, indicating a large change in the dipole moment of molecules upon excitation. A crystalline solid of DMAFP gives an excimer like emission at 566 nm due to the excitation of molecular aggregates. This is expected from the idealized crystal structure of the dye that belongs to the B-type class of Steven's classification. The ground and excited state protonation constants of DMAFP are calculated and amounted to 1.71 and 8.3, respectively. DMAFP acts as a good laser dye upon pumping with nitrogen laser (lambda(ex) = 337.1 nm) in chloroform, methylene chloride and dioxane and gives laser emission in the range 460-590 nm. The laser parameters such as the tuning range, gain coefficient (alpha), emission cross section (sigma(e)) and half-life energy (E-1/2) are calculated. The photoreactivity and net photochemical quantum yield of DMAFP in chloromethane solvents are also studied. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:727 / 733
页数:7
相关论文
共 44 条
[1]   DYE STABILITY UNDER EXCIMER-LASER PUMPING .2. VISIBLE AND UV DYES [J].
ANTONOV, VS ;
HOHLA, KL .
APPLIED PHYSICS B-PHOTOPHYSICS AND LASER CHEMISTRY, 1983, 32 (01) :9-14
[2]  
Balsells R.E., 1988, AUST J CHEM, V41, P104
[3]   PHOTOCHEMICAL-REACTION OF FULL-AROMATIC BETA-CARBOLINES IN HALOMETHANES .2. CHCL3 - ELECTRONIC-SPECTRA AND KINETICS [J].
BIONDIC, MC ;
ERRABALSELLS, R .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1994, 77 (2-3) :149-159
[4]   PHOTOCHEMICAL-REACTION OF BETA-CARBOLINES IN CARBON TETRACHLORIDE-ETHANOL MIXTURES [J].
BIONDIC, MC ;
ERRABALSELLS, R .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1990, 51 (03) :341-353
[5]  
BIONDIC MC, 1994, J PHOTOCH PHOTOBIO A, V77, P341
[6]  
BRIKS JB, 1969, PHOTOPHYSICS AROMATI
[7]  
CHU G, 1987, CHEM SOC FARADAY T, V183, P2533
[8]   Studies of solvation of ketocyanine dyes in homogeneous and heterogeneous media by UV/Vis spectroscopic method [J].
Das, PK ;
Pramanik, R ;
Banerjee, D ;
Bagchi, S .
SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY, 2000, 56 (14) :2763-2773
[9]  
DEMAS JN, 1971, J PHYS CHEM-US, V75, P991, DOI 10.1021/j100678a001
[10]  
Devalle JC, 1997, J PHYS CHEM A, V101, P3260