Photophysics of thionine in AOT and BHDC reverse micelles. Quenching of the triplet state by aliphatic amines studied by transient absorption spectroscopy was written by Porcal, Gabriela V.;Arbeloa, Ernesto M.;Bertolotti, Sonia G.;Previtali, Carlos M.. And the article was included in Journal of Photochemistry and Photobiology, A: Chemistry in 2017.HPLC of Formula: 122-18-9 The following contents are mentioned in the article:
The photophysics of thionine (3,7-diamino-5-phenothiazinium) (Th+) was investigated in reverse micelles (RMs) of sodium bis(2-ethylhexyl)sulfosuccinate (AOT) and benzyldimethylhexadecylammonium chloride (BHDC) with special emphasis on the triplet state processes. In RMs both the absorption and emission spectra of the dye present a red shift with respect to pure water. The absorption maximum wavelength and Stokes shift show a tendency towards the values in water, although do not reach them even with the higher water content examined The photophys. parameters are more affected by the water content in BHDC than in AOT. The triplet state of Th+ was investigated by the technique of laser flash photolysis. The T-T absorption spectrum presents a strong absorption band in the region between 770 and 800 nm, corresponding to the monoprotonated triplet form of the dye. This spectrum is red shifted with respect to water in the RMs. The triplet quenching by aliphatic amines was investigated. The triplet decay is well fitted by a bi-exponential function in the presence of the hydro-soluble triethanolamine (TEOA) in both RMs. This behavior is interpreted as the result of a very fast intramicellar quenching, followed by slow process that may be ascribed to an intermicellar exchange of amine mols. between RMs. The kinetic anal. showed that intermicellar exchange rate constant is two orders of magnitude more effective in BHDC than in AOT. Meanwhile, in the quenching by the hydrophobic tributylamine (TBA) the decay is mono-exponential. The amine is located preferentially in the bulk organic phase and the quenching mechanism involves the interaction of the amine with the monoprotonated triplet of dye reaching in the micellar interface. It is interesting to note that the apparent quenching rate constant by TBA is one order of magnitude lower than the exchange rate constant by TEOA. This study involved multiple reactions and reactants, such as N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9HPLC of Formula: 122-18-9).
N-Benzyl-N,N-dimethylhexadecan-1-aminium chloride (cas: 122-18-9) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.HPLC of Formula: 122-18-9
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics