Electrons were generated in the core of micelles formed by negatively charged sodium dodecyl sulfate (SDS) or positively charged dodecyltrimethylammonium chloride (DTAC) by photoionization of 3-methylindole embedded in the core. The electrons were hydrated after they moved out of the core to the outer aqueous phase. These processes were monitored with femtosecond time-resolved absorption spectroscopy.
View Article and Find Full Text PDFOrganic photoredox catalysis has become a useful tool for the development of metal-free radical reactions. Recently, we have reported that 1,4-bis(diphenylamino)naphthalene serves as an efficient photoredox catalyst for radical monofluoromethylation with -tosyl--monofluoromethyl--phenylsulfoximine . In this paper, we report the preparation and photo- and electrochemical properties of (diarylamino)naphthalene derivatives, 1,4-bis(di(--butylphenyl)amino)naphthalene , 1,5-bis(di(--butylphenyl)amino)naphthalene , and 1-(di(--butylphenyl)amino)naphthalene) , as supported by density functional theory (DFT) and time-dependent-DFT calculations.
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