Based on density functional theory(DFT) and time-dependent density functional theory(TD-DFT), the effects of substituent on the excited-state intramolecular proton transfer(ESIPT) process and photophysical properties ...Based on density functional theory(DFT) and time-dependent density functional theory(TD-DFT), the effects of substituent on the excited-state intramolecular proton transfer(ESIPT) process and photophysical properties of 2-(2’-hydroxyphenyl)-4-chloromethylthiazole(HCT) are studied. The electron-donating group(CH_(3), OH) and electronwithdrawing group(CF_(3), CHO) are introduced to analyze the changes of intramolecular H-bond, the frontier molecular orbitals, the absorption/fluorescence spectra, and the energy barrier of ESIPT process. The calculation results indicate that electron-donating group strengthens the intramolecular H-bond in the S_(1) state, and leads to an easier ESIPT process. The electron-withdrawing group weakens the corresponding H-bond and makes ESIPT process a little harder. Different substituents also affect the photophysical properties of HCT. The electron-withdrawing group(CF_(3), CHO) has a little effect on electronic spectra. The electron-donating group(CH_(3), OH) red-shifts both the absorption and fluorescence emission peaks of HCT, respectively, which causes the Stokes shift to increase.展开更多
文摘Based on density functional theory(DFT) and time-dependent density functional theory(TD-DFT), the effects of substituent on the excited-state intramolecular proton transfer(ESIPT) process and photophysical properties of 2-(2’-hydroxyphenyl)-4-chloromethylthiazole(HCT) are studied. The electron-donating group(CH_(3), OH) and electronwithdrawing group(CF_(3), CHO) are introduced to analyze the changes of intramolecular H-bond, the frontier molecular orbitals, the absorption/fluorescence spectra, and the energy barrier of ESIPT process. The calculation results indicate that electron-donating group strengthens the intramolecular H-bond in the S_(1) state, and leads to an easier ESIPT process. The electron-withdrawing group weakens the corresponding H-bond and makes ESIPT process a little harder. Different substituents also affect the photophysical properties of HCT. The electron-withdrawing group(CF_(3), CHO) has a little effect on electronic spectra. The electron-donating group(CH_(3), OH) red-shifts both the absorption and fluorescence emission peaks of HCT, respectively, which causes the Stokes shift to increase.
