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Vahur Mäemets

Researcher at University of Tartu

Publications -  17
Citations -  1569

Vahur Mäemets is an academic researcher from University of Tartu. The author has contributed to research in topics: Steric effects & Substituent. The author has an hindex of 12, co-authored 17 publications receiving 1440 citations. Previous affiliations of Vahur Mäemets include University of Bremen & National Academy of Sciences of Ukraine.

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Extension of the self-consistent spectrophotometric basicity scale in acetonitrile to a full span of 28 pKa units: unification of different basicity scales.

TL;DR: The earlier compiled self-consistent spectrophotometric basicity scale in acetonitrile (AN) was expanded to range from 3.8 to 32.0 pK(a) units, that is 28 orders of magnitude, and 54 new relative basicity measurements were carried out and 37 new compounds were introduced to the scale.
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Equilibrium acidities of superacids.

TL;DR: The current scale is complementary to the well-known H(0) scale in the information that it provides and is expected to be a useful tool in design, use, and further acidity measurements of superacidic molecules.
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Acid−Base Equilibria in Nonpolar Media. 2.1 Self-Consistent Basicity Scale in THF Solution Ranging from 2-Methoxypyridine to EtP1(pyrr) Phosphazene

TL;DR: The predictability of the basicity together with suitable spectral properties in the UV range make the phenylphosphazenes convenient neutral indicators in the high basicity range where the choice of neutral indicators is very limited.
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Guanidinophosphazenes: design, synthesis, and basicity in THF and in the gas phase.

TL;DR: Seven new nonionic superbasic phosphazene bases, tetramethylguanidino-substituted at the P atom, have been synthesized and are predicted to exceed the basicity of (dma)3P=NH by more than 40 powers of 10 and to surpass also thebasicity of the widely used commercial [(dma]3P =N]3p=N-t-Bu (t- BuP4) superbase.
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Acid-base equilibria in nonpolar media. 4. Extension of the self-consistent basicity scale in THF medium. Gas-phase basicities of phosphazenes.

TL;DR: Eleven new phenyl-substituted phosphazenes (P1, P3-, and P4-bases) have been synthesized by the Staudinger or the Kirsanov reactions, and the UV-vis spectrophotometric titration method was used to establish the relative basicity of them and to extend the ion-pair basicity scale for THF medium.