Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Yury I. Lyakhovetsky"'
Publikováno v:
Molecules, Vol 26, Iss 14, p 4383 (2021)
The rate of hydrolysis–condensation reaction of phenyltrichlorosilane in water-acetone solutions and the product yields were shown to significantly depend on the concentration of HCl (CHCl) in the solutions. The main product of the reaction was all
Externí odkaz:
https://doaj.org/article/bd21446ee2b34dbb86f9f028ea26a9db
Autor:
Irina M. Petrova, Yury I. Lyakhovetsky, Vladimir V. Chernyshev, Nikolai S. Ikonnikov, Nataliya N. Makarova
Publikováno v:
Molecules, Vol 24, Iss 22, p 4195 (2019)
The hydrolysis−condensation reactions of m-tolyl, m-chlorophenyl, and α-naphtyl-trichlorsilanes, (1, 2, and 3, respectively) in water-acetone solutions were examined for how they were influenced by the change in the concentration of HCl (CHCl). Th
Externí odkaz:
https://doaj.org/article/3a87eb9d906e4e5d83a1f9d23842aee5
Autor:
Yury I. Lyakhovetsky, Elena A. Shilova, Alexandra P. Pleshkova, Alexander I. Belokon, Sergey O. Yakushin, Boris L. Tumanskii
Publikováno v:
Journal of Spectroscopy, Vol 2016 (2016)
C60 was shown to react with organosilanes Me4Si, Ph2SiH2, Ph2MeSiH, Ph4Si, and α-naphthylphenylmethylsilane in the electron ionization ion source of a mass spectrometer with the transfer of the corresponding organic radicals (Me, Ph, and α-naphthyl
Externí odkaz:
https://doaj.org/article/ab4213419754467ca880eb23a8122dcf
Publikováno v:
Molecules
Molecules, Vol 26, Iss 4383, p 4383 (2021)
Volume 26
Issue 14
Molecules, Vol 26, Iss 4383, p 4383 (2021)
Volume 26
Issue 14
The rate of hydrolysis–condensation reaction of phenyltrichlorosilane in water-acetone solutions and the product yields were shown to significantly depend on the concentration of HCl (CHCl) in the solutions. The main product of the reaction was all
Autor:
Yuri S. Nekrasov, Albert G. Kornienko, Yury I. Lyakhovetsky, Yuri A. Borisov, Sergey S. Kiselev, Valeriya S. Velezheva, Nikolai S. Ikonnikov
Publikováno v:
International Journal of Analytical Mass Spectrometry and Chromatography. :1-16
The behavior of N-methylidenemalonates of 3-arylaminoindoles and p-dimetylamino-N-phenylanyline (M = ANa) was studied during their analysis with ESI mass spectrometer operated in negative (NI) and positive (PI) ion modes. Anions [A] and both [M + H]+
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 48(6)
o-Carborane, 9-I-o-carborane, 1-Me-o-carborane, and several other CH-acids, 9H-fluorene, 2-Br-9H-fluorene, and trimethylsylylacetylene, have been shown to react with C60 affording their monoadducts with fullerene, the reaction being mediated by Mn(OA
Autor:
A. I. Belokon, Alexandra P. Pleshkova, Boris Tumanskii, Elena A. Shilova, Sergey O. Yakushin, Yury I. Lyakhovetsky
Publikováno v:
Journal of Spectroscopy, Vol 2016 (2016)
C60was shown to react with organosilanes Me4Si, Ph2SiH2, Ph2MeSiH, Ph4Si, andα-naphthylphenylmethylsilane in the electron ionization ion source of a mass spectrometer with the transfer of the corresponding organic radicals (Me, Ph, andα-naphthyl) f
Autor:
Tatyana V. Strelkova, Nikolai S. Ikonnikov, N. N. Makarova, Irina M. Petrova, Yury I. Lyakhovetsky, Fedor M. Dolgushin, Alexander S. Peregudov, Zinaida S. Klemenkova
Publikováno v:
Polymers
Polymers; Volume 10; Issue 4; Pages: 422
Polymers, Vol 10, Iss 4, p 422 (2018)
Polymers; Volume 10; Issue 4; Pages: 422
Polymers, Vol 10, Iss 4, p 422 (2018)
Oligo- and polycyclosiloxanes were obtained by the polycondensation of (tetrahydroxy)(tetraaryl)cyclotetrasiloxanes in equilibrium and non-equilibrium conditions in the presence and absence of montmorillonite (MMT). Their composition and the structur
Publikováno v:
Journal of the American Society for Mass Spectrometry. 24:579-588
C60 reacted with PhH, PhCl, BnH, BnNH2, and o-C2H2B10H10 in the electron impact (EI) ion source of a mass spectrometer at 300 °C forming phenyl, benzyl, and o-carboranyl adducts, respectively, stabilized by hydrogen addition and loss. Besides, the a
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 45(42)
The phosphonylation of C60 with HP(O)(OAlk)2 and Mn(OAc)3·2H2O has been considered to occur via a free radical (FR) path involving intermediate radicals ˙P(O)(OAlk)2. The present study provides evidence in support of another mechanism for the react