详细信息
Synthesis and Photochromism of Naphthopyrans Bearing Naphthalimide Chromophore: Predominant Thermal Reversibility in Color-Fading and Fluorescence Switch ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Synthesis and Photochromism of Naphthopyrans Bearing Naphthalimide Chromophore: Predominant Thermal Reversibility in Color-Fading and Fluorescence Switch
作者:Song, Liwen[1,2];Yang, Yuheng[1,2];Zhang, Qiong[1,2,3];Tian, He[1,2];Zhu, Weihong[1,2]
机构:[1]E China Univ Sci & Technol, Shanghai Key Lab Funct Mat Chem, Key Lab Adv Mat, Shanghai 200237, Peoples R China;[2]E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China;[3]AlbaNova Univ Ctr, Royal Inst Technol, Dept Theoret Chem & Biol, S-10691 Stockholm, Sweden
年份:2011
卷号:115
期号:49
起止页码:14648
外文期刊名:JOURNAL OF PHYSICAL CHEMISTRY B
收录:;EI(收录号:20115114609269);WOS:【SCI-EXPANDED(收录号:WOS:000297608600036)】;
基金:This work was financially supported by NSFC/China, the Oriental Scholarship, SRFDP 200802510011, and the Fundamental Research Funds for the Central Universities (WK1013002).
语种:英文
外文关键词:Photolysis - Fluorescence - Color - Incident light - Cleaning - Transient absorption spectroscopy - Bleaching - Chromophores - Lenses - Refractive index
摘要:Two novel photochromic naphthopyrans containing naphthalimide moieties (Nip1 and Nip2) were studied in solution under flash photolysis conditions, exhibiting highly photochromic response, rapid thermal bleaching rate and good fatigue-resistance. Owing to the different N-substituted imide groups at the naphthalimide units, the thermal bleaching rate of Nip2 bearing phenyl on the naphthalimide unit is found to be approximately 2 times that of Nip1 bearing n-butyl, indicating that the photochromic properties can be modulated with introduction of different functional groups on the naphthalimide unit. In Nip1 and Nip2, the strong electron-withdrawing effect of the imide group incorporated at the naphthalimide moiety maintains several merits: (i) shifting absorption bands to longer wavelength, (ii) beneficial to an enhancement in the ratio of transoid-cis (TC) isomer and an increase in the transformation rate from transoid-trans (TT) to TC with respect to reference compound NP, and (iii) resulting in a preferable color bleaching rate and fading absolutely to their colorless state with thermal reversibility. As demonstrated in the system of NP, the slow transformation process from TT to TC might be the predominant dynamic step in thermal back process, leading to the residual color of NP being only faded to its original colorless state by visible light irradiation. The optical densities of colored forms for Nip1 and Nip2 are dependent upon the intensity of incident light, ensuring a possible application in the manufacture of ophthalmic lenses and smart windows. Moreover, the fluorescence of Nip1 and Nip2 can be switched on and off by photoinduced conversion between the closed and open forms.
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