{"title":"芳香羧酸酯的2型光消除反应","authors":"J. Barltrop, J. Coyle","doi":"10.1039/J29710000251","DOIUrl":null,"url":null,"abstract":"Aromatic esters of the type Ar·CO2·CH2·CHR1R2 are found to undergo a photoelimination reaction from both singlet and triplet excited states, though the process is inefficient from states of either multiplicity. Rate constants for the primary steps are evaluated for the systems p-MeO·C6H4·CO2·CH2·CHR1R2(R1= Me; R2= H, Me). Absorption and emission data suggest that the lowest singlet and triplet states in all the esters studied are ππ* in nature.","PeriodicalId":17268,"journal":{"name":"Journal of The Chemical Society B: Physical Organic","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"1971-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":"{\"title\":\"Type 2 photoelimination reaction of esters of aromatic carboxylic acids\",\"authors\":\"J. Barltrop, J. Coyle\",\"doi\":\"10.1039/J29710000251\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Aromatic esters of the type Ar·CO2·CH2·CHR1R2 are found to undergo a photoelimination reaction from both singlet and triplet excited states, though the process is inefficient from states of either multiplicity. Rate constants for the primary steps are evaluated for the systems p-MeO·C6H4·CO2·CH2·CHR1R2(R1= Me; R2= H, Me). Absorption and emission data suggest that the lowest singlet and triplet states in all the esters studied are ππ* in nature.\",\"PeriodicalId\":17268,\"journal\":{\"name\":\"Journal of The Chemical Society B: Physical Organic\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1971-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Chemical Society B: Physical Organic\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1039/J29710000251\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Chemical Society B: Physical Organic","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1039/J29710000251","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Type 2 photoelimination reaction of esters of aromatic carboxylic acids
Aromatic esters of the type Ar·CO2·CH2·CHR1R2 are found to undergo a photoelimination reaction from both singlet and triplet excited states, though the process is inefficient from states of either multiplicity. Rate constants for the primary steps are evaluated for the systems p-MeO·C6H4·CO2·CH2·CHR1R2(R1= Me; R2= H, Me). Absorption and emission data suggest that the lowest singlet and triplet states in all the esters studied are ππ* in nature.