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RIMap-RISC: a transcriptome-wide database of structurally modeled human microRNA interactions. [PDF]

Genome Biol
Chasles S, Gaillard-Duchassin Z, Quenneville J, Lemaire M, Gagnon E, Major F.   +5 more
europepmc   +1 more source

Competitive Inhibition as a Tool to Modulate and Predict Dynamic Hydrogel Mechanics. [PDF]

ACS Cent Sci
Claiborne AD, Mekcham S, Lee OA, Hill MR.   +3 more
europepmc   +1 more source

Synergistic cation-facet effects boost alkaline hydrogen evolution kinetics on stepped Pt surfaces. [PDF]

Commun Chem
Zhang Q, Sun P, Li H, Duan Z.
europepmc   +1 more source

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Dissociation constants of thymolphthalexone

Talanta, 1979
For the dissociation constants of thymolphthalexone the following values have been found: pK(3) = 7.03 +/- 0.02, pK(4) = 8.05 +/- 0.09 (by potentiometric titration), pK(5) = 10.83 +/- 0.10, pK(6) = 12.99 +/- 0.11 (by spectrophotometry). They were determined at I = 0.4 and at 25 degrees.
A, Hulanicki, S, Głab
openaire   +2 more sources

Dissociation constants of arsenazo III

Talanta, 1986
Commercial samples of Arsenazo III were found to be appreciably impure even after purification as the barium salt. Chromatography on silica gel followed by crystallization yielded a pure sample of the ethanol solvate of the free acid. The dissociation constants of the acid were determined potentiometrically at 25 degrees and I = 0.1 (NaClO(4)).
I, Nemcová, B, Metal, J, Podlaha
openaire   +2 more sources

Dissociation constants of carboxymethyloxysuccinic acid

Talanta, 1974
The dissociation constants of carboxymethyloxysuccinic acid (CMOS) have been measured at 25 degrees and an ionic strength of 0.1M in sodium perchlorate. The values found were: pK(1) = 2.52, pK(2) = 3.77 and pK(3) = 5.00. CMOS is thus seen to be rather stronger than its isomer citric acid.
C E, Rodriguez, C D, Devine
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Acid Dissociation Constants of Phenylalkanolamines

Journal of Pharmaceutical Sciences, 1962
The acid dissociation constants of phenylephrine, synephrine, and tyramine were investigated by the new spectrophotometric method of Edsall. Epinephrine was studied by a titration and complexation method. It is concluded from analysis of the spectral data that the phenolic function is a stronger acid than the alkylammonium group.
S, RIEGELMAN, L A, STRAIT, E Z, FISCHER
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