1986
DOI: 10.1139/v86-139
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Electron donor–acceptor complexes between naphthylamines and methyl viologen in aqueous sodium dodecyl sulphate solution

Abstract: The electron donor–acceptor (EDA) interaction between methyl viologen (MV2+) and 1-naphthylamine (1NA), 2-naphthylamine (2NA), and N,N-dimethyl-1-naphthylamine (DMA) was studied in water and in aqueous sodium dodecyl sulphate (SDS). The experimental values of the association constants in water were 8.9, 9.8, and 2.8 M−1 for 1NA, 2NA, and DMA, respectively. In the presence of SDS the observed values were very much higher and strongly dependent upon the detergent concentration. The enhancement in the interaction… Show more

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Cited by 12 publications
(5 citation statements)
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“…Notably, simple mixing of DMA with MV 2+ also results in similar brown color complex with an absorption band centered at 480 nm (Figure S5 of the SI). Similar results have been observed earlier for various amine-containing molecules and MV 2+ pair due to the formation of weak donor–acceptor ground state complex formation. , Addition of MV 2+ first followed by the addition of DMA results in similar kinds of PL quenching of PND (Figure S6 of the SI). Here it is important to note that the PL peak position of PND remains unchanged upon addition of DMA and MV 2+ , indicating the absence of any specific association of PND with DMA and MV 2+ .…”
Section: Resultssupporting
confidence: 88%
“…Notably, simple mixing of DMA with MV 2+ also results in similar brown color complex with an absorption band centered at 480 nm (Figure S5 of the SI). Similar results have been observed earlier for various amine-containing molecules and MV 2+ pair due to the formation of weak donor–acceptor ground state complex formation. , Addition of MV 2+ first followed by the addition of DMA results in similar kinds of PL quenching of PND (Figure S6 of the SI). Here it is important to note that the PL peak position of PND remains unchanged upon addition of DMA and MV 2+ , indicating the absence of any specific association of PND with DMA and MV 2+ .…”
Section: Resultssupporting
confidence: 88%
“…During photolysis, the ampoules were open to the atmosphere. observed in micelle-catalyzed bimolecular reactions (19) and it has also been observed in the system naphthylamines-MV2 pseudophase could affect the equilibrium, thus changing the in SDS (20).…”
Section: Absolute Isomerization Quantum Yieldsmentioning
confidence: 58%
“…The results can be analyzed by Under our experimental conditions, the fraction of MV+' means of the following equations: bound to micelles is nearly unit (20), as is the case for stilbenes 2 ' [Dl,, a straight line is obtained (Fig. 2) and Kc, can be calculated from the slope.…”
Section: Resultsmentioning
confidence: 99%
“…Type III viologen materials are solid in all redox states during usage. Researchers have developed various viologen-functionalized materials [5][6][7] such as viologen-modified nano-crystals [8][9][10][11][12], viologen nano-composite [13], polymers containing viologen [14,15], dialkyl and diaryl viologens [3,12,[16][17][18][19][20][21][22][23][24], viologen-functionalized hyper-branched and viologen-functionalized dendrimer [16,[25][26][27][28], which have different solubility and EC device efficiency.…”
Section: Introductionmentioning
confidence: 99%