https://scholars.lib.ntu.edu.tw/handle/123456789/177699
標題: | Efficient photocycloaddition of phenanthroquinones with simple olefins | 作者: | Ho, Jinn-Hsuan Ho, Tong-Ing Chen, Ti-Horng Yuan, L. Chow |
關鍵字: | Excited state cycloaddition;o-Quinone triplet state reaction;Stepwise radical reaction;Stereo- & regio-specificity;Charge transfer contribution | 公開日期: | 2001 | 出版社: | Taipei:National Taiwan University Dept Chem Engn | 起(迄)頁: | - | 來源出版物: | Journal of Photochemistry & Photobiology A: Chemistry (138),111–122 | 摘要: | A series of substituted phenanthroquinones (PQ’s) was prepared, their phosphorescence spectra & decay rate constants, cyclic voltammograms, & photoreaction in the presence of tetramethylethylene (TME) were investigated.With 450 nm irradiation their triplet excited state cyclized with TME to give the corresponding dioxenes, 20,20,30,30-tetramethyl-10,40-dioxa-10,20,30,40-tetrahydrotriphenylene, cleanly & much faster than that with 300 nm irradiation. The pattern of the reaction was effected weakly in random fashion by the substituent at the 3-position of PQ’s. The photocycloaddition, as exemplified by PQ itself, is so efficient that it occurred even by room light & during optical spectroscopic recordings; its limiting quantum yield in benzene is established to be unity with 450 nm irradiation. It owes the unusual efficiency to a long lifetime of the PQ triplet excited state with the n–p configuration, & to the successful cyclization in every diffusion controlled collision as implicated by TME quenching of PQ phosphorescence intensity in CCl4 solution. The triplet excited state reaction was supported by competitive quenching of the dioxene formation by triplet quenchers as well as by oxygen. These PQ’s do not fluoresce in solution, but show phosphorescence in solid solution with lifetimes of about 10 ms & in CCl4 solution with lifetimes in the order of 100ms in the room temperature range. PQ’s with 3-cycano, 3-chloro, 3-methoxy, & without substitutions photocyclized to cyclohexene to give the corresponding dioxenes with small stereochemical scrambles, that was interpreted that the extent of electron transfer in the 1,6-diradical stage is small. Similar photocycloadditions to isobutene gave a 1:1 mixture of two regio-isomers, this was taken as evidence for a direct radical attack on olefins to give 1,6-diradical intermediates. |
URI: | http://ntur.lib.ntu.edu.tw//handle/246246/2006111501233281 | 其他識別: | 246246/2006111501233281 |
顯示於: | 化學系 |
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