E
Ernestas Gaidamauskas
Researcher at Colorado State University
Publications - 23
Citations - 1784
Ernestas Gaidamauskas is an academic researcher from Colorado State University. The author has contributed to research in topics: Micelle & Aqueous solution. The author has an hindex of 14, co-authored 22 publications receiving 1632 citations. Previous affiliations of Ernestas Gaidamauskas include Vilnius University.
Papers
More filters
Journal ArticleDOI
The chemistry and biochemistry of vanadium and the biological activities exerted by vanadium compounds.
TL;DR: Aqueous V(III) Chemistry 877 6.2.1.
Journal ArticleDOI
Is vanadate reduced by thiols under biological conditions? Changing the redox potential of V(V)/V(IV) by complexation in aqueous solution.
Debbie C. Crans,Boyan Zhang,Ernestas Gaidamauskas,Anastasios D. Keramidas,Gail R. Willsky,Christopher R. Roberts +5 more
TL;DR: This work demonstrates that both vanadium(IV) and (V)-thiol complexes form and that redox chemistry also takes place and it is now possible to understand the distribution of vanadium in oxidation states (IV and V) in the presence of glutathione, cysteine, and other thiols and begin to evaluate the forms of the vanadium compounds that exert a particular biological effect.
Journal ArticleDOI
The Chemistry and Biochemistry of Vanadium and the Biological Activities Exerted by Vanadium Compounds
Journal ArticleDOI
Deprotonation of beta-cyclodextrin in alkaline solutions.
TL;DR: Variable pH (13)C NMR and (1)H NMR spectroscopic studies of the beta-cyclodextrin (beta-CD) in alkaline aqueous solutions revealed that beta-CD does not deprotonate at pH<12.0.
Journal ArticleDOI
Effect of micellar and reverse micellar interface on solute location: 2,6-pyridinedicarboxylate in CTAB micelles and CTAB and AOT reverse micelles.
TL;DR: Spectra recorded of the dipic-probe at various pH values demonstrate that both CTAB micelles and reverse micellar interfaces are different than those reported in aqueous solution and in AOT/isooctane reverse miceLLes and point to headgroup charge as being a key factor determining the direction of chemical shift change and the depth of solute penetration.