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The synthesis and time-resolved spectra of indolinospironaphthopyrans | |
Wu, XY; Wu, CT; Wang, WF(王文峰); Yao, SD(姚思德) | |
1998 | |
Source Publication | CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE
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ISSN | 0251-0790 |
Volume | 19Issue:2Pages:246 |
Abstract | Three indolinospironaphthopyrans: 1',3'-dihydro-1',3',3'-trimethyl-spiro[2H-indole-2,3-(3H) naphtho [2,1-b]pyran], 1',3'-dihydro-3',3'-dimethyl-1-(2-hydroxyethyl)-spiro[2H-indole-2,3-(3H)naphtho[2,1-b]pyran], 1',3'-dihydro-3',3'-dimethyl-1-(5-iodo-3-oxypentyl)-spiro [2H-indole-2,3-(3H)naphtho[2,1-b]pyran] were synthesized, and their photochromic reactions were studied using nanosecond laser photolysis technique. Photolysis of these compounds in acetonitrile and in tetrahydrofuran leads to the formation of the long-lived photomerocyanine (PMC) as the predominant photoproduct. The formation of the PMC occurs owing to C-O bond opening, mainly directly from the excited single state of the spiropyran(SP). From the absorption bands, it has been speculated that the substituents of the nitrogen atom of the indole ring influence the structural characteristics of the PMC mainly through steric hindrance effects. A potential energy surface model is established to explain the results. |
Indexed By | SCI |
Language | 英语 |
Funding Project | 应物所项目组 |
WOS ID | WOS:000072402000021 |
Citation statistics | |
Document Type | 期刊论文 |
Identifier | http://ir.sinap.ac.cn/handle/331007/10234 |
Collection | 中科院上海原子核所2003年前 |
Recommended Citation GB/T 7714 | Wu, XY,Wu, CT,Wang, WF,et al. The synthesis and time-resolved spectra of indolinospironaphthopyrans[J]. CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1998,19(2):246. |
APA | Wu, XY,Wu, CT,Wang, WF,&Yao, SD.(1998).The synthesis and time-resolved spectra of indolinospironaphthopyrans.CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,19(2),246. |
MLA | Wu, XY,et al."The synthesis and time-resolved spectra of indolinospironaphthopyrans".CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE 19.2(1998):246. |
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