Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Ya. R. Tymyanskii"'
Publikováno v:
Journal of Applied Spectroscopy. 62:454-457
Autor:
M. I. Knyazhanskii, Ya. R. Tymyanskii, L. O. Atovmyan, Oleg A. Dyachenko, G. N. Dorofeenko, S. M. Aldoshin
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 30:1864-1872
1. A significant difference was found in the luminescence characteristics of 1-(2-hydroxyphenyl)- and 1-(4-hydroxyphenyl)-2,4,6-triphenylpyridinium perchlorates at various temperatures. At 293°K the luminescence of both compounds in the crystalline
Publikováno v:
Journal of Applied Spectroscopy. 25:1015-1018
Publikováno v:
Chemistry of Heterocyclic Compounds. 24:1091-1094
2,6-Diphenyl-4-(5-R-2-furyl) pyrylium and 2,4-diphenyl-6-(5-bromo-2-furyl) pyrylium perchlorates and the corresponding pyridines and 1-methylpyridinium perchlorates were synthesized. On the basis of the UV and PMR spectra it was concluded that there
Autor:
Ya. R. Tymyanskii, E. Lunt, Bushra J. Agha, M. I. Knyazhanskii, A. I. Pyshchev, Alan R. Katritzky, G. Z. de Ville
Publikováno v:
Chemistry of Heterocyclic Compounds. 20:1245-1254
New 1,2-diaryl- and 1,2,6-triarylpyridinium salts, containing various five- and six-membered heteroaromatic substituents in the 1, 2, and 6-positions of the pyridinium ring, were synthesized. New tetra- and hexacyclic compounds were prepared by photo
Autor:
L. O. Atovmyan, Ya. R. Tymyanskii, A. I. Pyshchev, Oleg A. Dyachenko, M. I. Knyazhanskii, S. M. Aldoshin
Publikováno v:
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 31:478-482
It was found by UV spectroscopy and x-ray diffraction analysis that the photocyclization of 1-(3'-halophenyl)-2,4,6-triphenylpyridiniurn cations leads to stable 1,3-diphenyl-11-chloro(bromo)-azoniatriphenylene cations.
Publikováno v:
Chemistry of Heterocyclic Compounds. 14:990-993
Nitro and amino derivatives of pyrido[1,2-f]phenanthridinium perchlorate were synthesized by the Pschorr method and by photocyclodehydrogenation from N-(nitrophenyl)-or N-(aminophenyl)pyridinium perchlorates. The mechanism of the photoconversion was
Publikováno v:
Journal of Applied Spectroscopy. 42:394-398
Publikováno v:
Chemistry of Heterocyclic Compounds. 20:1262-1266
The spectral-fluorescent and photochemical properties of 1-naphthyl-2,4-di- and 2,4,6-triphenylpyridinium perchlorates were investigated in solutions at 293 and 77 °K. The anomalously large Stokes shift of the fluorescence was due to the adiabatic c
Publikováno v:
Chemistry of Heterocyclic Compounds. 10:696-698
The electronic spectra of a number of benzylidene derivatives of N-aminoarylpyridinium perchlorates are associated with absorption localized on the individual pyridinium and azomethine fragments and with intramolecular charge transfer (ICT) from the