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Tag Archive for Гуринов

Вышла статья с участием сотрудников РЦ

Gurinov, A. A.; Mauder, D.; Akcakayiran, D.; Findenegg, G. H.; Shenderovich, I. G.

“Does Water Affect the Acidity of Surfaces? The Proton-Donating Ability of Silanol and Carboxylic Acid Groups at Mesoporous Silica.”

ChemPhysChem 2012, 13 (9), 2282-2285.
DOI: 10.1002/cphc.201200204

Solvation at the interphase:

A study of the influence of water on the effective acidity of silanol and carboxylic acid groups of propionic acid functionalized SBA-15 reveals that to affect the proton-donating ability of an acidic group at the surface, water should be able to form a solvation shell around that group. As a result, water does not affect the acidity of native SBA-15 but dramatically enhances that of SBA-15 functionalized with propionic acid moieties.

Сотрудники РЦ приняли участие в русско-финской конференции

Russian-Finnish Conference on Technology transfer, Entrepreneurship and Research Infrastructure management прошла в университете Аалто, Финляндия.

 

 

 

Key themes at Conference:

  • Gateway into Finnish Innovation systems
  • Experience how to build up an effective open innovation space.
  • Training in technology transfer, entrepreneurship and research infrastructure management
  • Networking possibility to meet Finnish experts.

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Статью с участием сотрудников РЦ поместили на обложку журнала Journal of Physical Organic Chemistry

Gorobets, N. Y.; Yermolayev, S. A.; Gurley, T.; Gurinov, A. A.; Tolstoy, P. M.; Shenderovich, I. G.; Leadbeater, N. E.

“Difference between 1H NMR signals of primary amide protons as a simple spectral index of the amide intramolecular hydrogen bond strength.”

J. Phys. Org. Chem. 2011, 25 (4), 287-295.
DOI: 10.1002/poc.1910

Abstract

The effect of the intramolecular H-bonding of the primary amide group on the spectral properties and reactivity of this group towards electrophiles has been studied in systematic rows of 1,2,5,6,7,8-hexahydro-7,7-dimethyl-2,5-dioxo-1-R-quinoline-3-carboxamides and 2-aryliminocoumarin-3-carboxamides using 1H and 15N NMR spectroscopy and the kinetics of model reactions. Read more