AbStIXt Acrylanude 1s a hydrophdx fluorescence quencher that nonetheless readily enters the hydmpholnc mterlor of detergent nucelles m aqueous solution No such movement IS observed between bulk aqueous and orgamc phases &molecular quenchmg constants m both normal and reverse nucelles mchcate that qu
Fluorescence quenching by acrylamide in micellar solutions
โ Scribed by M.A. Rubio; E.A. Lissi
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 435 KB
- Volume
- 71
- Category
- Article
- ISSN
- 1010-6030
No coin nor oath required. For personal study only.
โฆ Synopsis
Quenching of the fluorescence of methylpyrene and anthracene derivatives by acrylamide in micelles follows a linear Stern-Volmer relationship. Incorporation of the fluorophores inside the micelles leads to a decrease in the quenching rates, and the bimolecular rate constants, obtained in terms of the analytical acrylamide concentration, are considerably smaller in cetyltrimethylammonium chloride (CTAC) and poly(oxyethylene)dodecyl ether (Brij 35) micelles than in sodium dodecylsulphate (SDS) micelles. By comparison of these data with those obtained using indole derivatives, it is concluded that the strong protection observed, particularly in CTAC micelles, is due to a reduction in the intramicellar bimolecular quenching rate constant. Increasing the SDS concentration or the addition of n-hexanol or NaCl leads to a reduction in the interaction rate due to partial dehydration of the micellar interface.
๐ SIMILAR VOLUMES
The fluorescence from the St state of pyrene solubilized within the hydrophobic region of sodium dodecyl sulfate micelles has been studied as a function of concentration of some cationic additives to the aqueous phase. At concentrations of added quencher below ca\_ 10v3 mol dm -3 the fluorescence de
Dynamic fluorescence quenching measurements have been performed on pyrene derivatives (pyrene (Py), 1-pyrenebutanoic acid (PBA), and 1-pyrenedodecanoic acid (PDA)), using as quenchers nitroxide free radicals (2,2,6,6-tetramethyl-1,1-piperidinyloxyl, 4hydroxy-2,2,6,6-tetramethyl-1,1-piperidinyloxyl,
The ratio of peak III to peak I intensities of the so-called III and I fluorescence bands of pyrene increases dramatically when cupric ions are used as quenchers for pyrene emission in sodium dodecyl sulfate micelles. These results indicate a decrease in the polarity sensed by the probe when its lif