CAS OpenIR  > 中科院上海原子核所2003年前
Electronic spectroscopy and photochromic mechanism of bis-Schiff bases, N,N'-bis(2-hydroxy-1-naphthylidene)-1,4-phenyldiamine
Ming, YF; Huang, ZN; Fan, MG; Xu, BA; Jin, S; Yao, SD(姚思德)
1997
Source PublicationSCIENCE IN CHINA SERIES B-CHEMISTRY
ISSN1001-652X
Volume40Issue:4Pages:373
AbstractThe steady state and transient state absorption spectra and fluorescence spectra of N, N'-bis(2-hydroxy-1-naphthylidene )-1, 4-phenyldiamine (BNP) in cyclohexane and acetonitrile were determined. The photochromic mechanism was discussed. In nonpolar solvents, BNP exists mainly in the enol form and has the absorption maximum in the UV region. In polar solvents, however, both the enol and proton transfer tautomer are formed, but the former is the main one. Fluorescence emissions result from the excited state of proton transfer product.
Indexed BySCI
Language英语
Funding Project应物所项目组
WOS IDWOS:A1997XR16500006
Citation statistics
Document Type期刊论文
Identifierhttp://ir.sinap.ac.cn/handle/331007/9955
Collection中科院上海原子核所2003年前
Recommended Citation
GB/T 7714
Ming, YF,Huang, ZN,Fan, MG,et al. Electronic spectroscopy and photochromic mechanism of bis-Schiff bases, N,N'-bis(2-hydroxy-1-naphthylidene)-1,4-phenyldiamine[J]. SCIENCE IN CHINA SERIES B-CHEMISTRY,1997,40(4):373.
APA Ming, YF,Huang, ZN,Fan, MG,Xu, BA,Jin, S,&Yao, SD.(1997).Electronic spectroscopy and photochromic mechanism of bis-Schiff bases, N,N'-bis(2-hydroxy-1-naphthylidene)-1,4-phenyldiamine.SCIENCE IN CHINA SERIES B-CHEMISTRY,40(4),373.
MLA Ming, YF,et al."Electronic spectroscopy and photochromic mechanism of bis-Schiff bases, N,N'-bis(2-hydroxy-1-naphthylidene)-1,4-phenyldiamine".SCIENCE IN CHINA SERIES B-CHEMISTRY 40.4(1997):373.
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