ESTUDO DO EFEITO DE SUBSTITUINTES NA FOTOQUÍMICA DE TIOXANTONA POR FOTÓLISE POR PULSO DE LASER EM NANOSSEGUNDO / STUDY OF THE EFFECT OF substituents on the photochemical Thioxanthone flash photolysis BY LASER IN nanosecond

AUTOR(ES)
FONTE

IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia

DATA DE PUBLICAÇÃO

15/06/2010

RESUMO

By laser flash photolysis, the photo-reactivity of the triplet excited state of thioxanthone derivatives (2BTX, 2MeOTX, 2PrOTX and 2MeTX) was studied. The maximum wavelength and triplet time life of theirs transients are solvent dependents, a blue-shift is observed with the change of no polar to polar middle and still more in hydroxyl solvent. The triplet spectrum with hydrogen-donor solvents shows a slower broad band between 430-460nm that again is observed with hydrogen-donor quenchers, this band is attributed to ketyl radical. The broad bands in 410 and 500nm are attributed to phenoxyl, indolyl radicals and ions radicals as intermediates, respectively. The higher values to hydrogen transference from alcohols (~105 M-1s-1) and allylic hydrocarbons and phenols (~109 M-1s-1) are attributed to the triplet excited state of lower energy have a mixture of excited states with predominant character of the excited state with nπ*. The no dependence to substituted-phenols on Kq and the approximated values between then and TEA, DABCO and indole (~109 M-1s-1) are indicating a mechanism by electron-transference followed a faster proton transference from an exciplex. The quenching rate contants by transfer of energy from trans-stilbene, 1-methylnaphthalene and 1,3-cyclohexadiene are controlled by diffusion for 2MeTX remaining triplet energy over 61 kcal.mol-1, as observed for TX. For the other substituents was a decrease in triplet energy is getting between 53 and 61 kcal.mol-1.

ASSUNTO(S)

tioxantona fotoquímica estado exitado triplete quimica organica thioxanthone photochemistry triplet state exitado

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