Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Vladimir E. Terekhov"'
Autor:
A. V. Babkin, Alexey A. Bogolyubov, Boris Bulgakov, Vladimir E. Terekhov, Oleg S. Morozov, Alexey V. Kepman, E.S. Afanaseva, Avdeev Viktor
Publikováno v:
Mendeleev Communications. 30:796-798
A new low melting highly hydrolytically stable phthalonitrile monomer containing silane fragment was synthesized by a three-step procedure and cured to obtain a highly heatresistant thermoset. The polymer demonstrated the glass transition temperature
Autor:
Oleg S. Morozov, E.S. Afanaseva, Boris Bulgakov, Alexey V. Kepman, Avdeev Viktor, A. V. Babkin, Vladimir E. Terekhov
Publikováno v:
Mendeleev Communications. 30:671-673
Fluorinated phthalonitrile monomers exhibit low activity in polymerization initiated by a wide range of curing agents of various nature. On the contrary, the use of fluorinated diamines as hardeners for common non-fluorinated phthalonitrile monomer a
Autor:
Alexey V. Kepman, S.S. Nechausov, Boris Bulgakov, Vladimir E. Terekhov, A. V. Babkin, V.V. Aleshkevich, Avdeev Viktor, E.S. Afanaseva
Publikováno v:
Reactive and Functional Polymers. 139:34-41
Bis(4-cyanophenyl) phenyl phosphate (CPP) is introduced for the first time as a viscosity reducing comonomer for phthalonitrile resins. In comparison to the common phthalonitrile resins, the blends of CPP with 4,4′-[benzene-1,3-diylbis(oxy)]diphtha
Autor:
Boris Bulgakov, Vladimir E. Terekhov, Alexey V. Kepman, V.V. Aleshkevich, E.S. Afanaseva, A. V. Babkin, S.S. Nechausov, Avdeev Viktor
Publikováno v:
Data in Brief
Hydrolysis data for Bis(4-cyanophenyl) phenyl phosphate (CPP), introduced as a reactive diluent for phthalonitrile monomers, under pH 4, 7 and 10 are presented. Conversion/time plots collected by HPLC analysis, typical chromatograms and NMR spectra o
Autor:
Artur V. Eshtukov, Vladimir E. Terekhov, Maxim A. Topchiy, Pavel S. Gribanov, Yana I. Lichtenstein, Mikhail S. Nechaev, Andrey F. Asachenko, Yulia D. Golenko
Publikováno v:
Green Chemistry. 18:5984-5988
Fischer's approach towards the synthesis of aryl azides and triazinoles from diazonium salts and hydroxylammonium chloride (phenylhydraxylamine) was reinvestigated and optimized. The new methodology enables the preparation of aryl azides and triazino