REDOX REACTIONS INVOLVING N-ALKYL-DIHYDRONICOTINAMIDES
Abstract:
<p align="justify"> Electron transfer reactions involving a series of N-alkyl-dihydronicotinamides (R-NAH) as donors were studied in homogenous solvents and in micellar media. In particular, the redox chemistry and kinetics of the reduction of methylene blue and cytochrome-C, by varying the alkyl chain length (R = C<sub>4</sub>, C<sub>8</sub>, C<sub>12</sub>) were investigated The schemes proposed for functionalized surfactants of nicotinamide suggest photochemical conversion based on light-induced electron-transfer reactions. </p>
<p align="justify"> Electron transfer reactions involving a series of N-alkyl-dihydronicotinamides (R-NAH) as donors were studied in homogenous solvents and in micellar media. In particular, the redox chemistry and kinetics of the reduction of methylene blue and cytochrome-C, by varying the alkyl chain length (R = C<sub>4</sub>, C<sub>8</sub>, C<sub>12</sub>) were investigated The schemes proposed for functionalized surfactants of nicotinamide suggest photochemical conversion based on light-induced electron-transfer reactions. </p>
DOI: 10.48141/SBJCHEM.v2.n2.1994.122_1994.pdf
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