Zobrazeno 1 - 10
of 18
pro vyhledávání: '"S. I. Luiksaar"'
Autor:
V. A. Barachevskii, Valery A. Vasnev, S. I. Luiksaar, B. A. Izmailov, O. I. Kobeleva, L. I. Komarova, Tatyana M. Valova, E. N. Rodlovskaya, M. M. Krayushkin
Publikováno v:
Polymer Science Series B. 53:352-357
Photochromic coatings immobilized on the surface of polyarylate films are prepared on the basis of fulgimides, oligosiloxanes, and oligosilazanes. The irradiation of coatings with UV light at a wavelength of @380 nm and visible light at a wavelength
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd8a0ae1eb9c42d9eabaf4ccabc10a6a
https://doi.org/10.1134/s156009041105006x
https://doi.org/10.1134/s156009041105006x
Autor:
Vladimir N. Yarovenko, B. V. Nabatov, M. M. Krayushkin, I. A. Platonova, L. K. Karabaeva, S. I. Luiksaar, V. A. Barachevski, Igor V. Zavarzin
Publikováno v:
Chemistry of Heterocyclic Compounds. 47:229-236
The precursors and hybrid compounds, including photochromic fulgimides and fluorescent benzothiazolylthienothiophene units, have been synthesized. Spectroscopic investigations by absorption and fluorescence methods showed that fulgimide hybrids displ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e73b2a623a2770d506cd96f84dac6ddb
https://doi.org/10.1007/s10593-011-0745-9
https://doi.org/10.1007/s10593-011-0745-9
Autor:
Anatolii S. Burlov, V. A. Barachevskii, V. A. Kogan, O. I. Kobeleva, Leonid D. Popov, Igor N. Shcherbakov, M. M. Krayushkin, Tatyana M. Valova, S. I. Luiksaar
Publikováno v:
Russian Journal of General Chemistry. 80:1847-1852
On the basis of N-aminofulgimide two new photochromic compounds of the fulgimide class were synthesized. The performed spectral-kinetic studies have shown that the obtained fulgimide derivatives suffer thermally irreversible transformation similar to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c848c7bb188c4428f64318895b3645ab
https://doi.org/10.1134/s1070363210090227
https://doi.org/10.1134/s1070363210090227
Autor:
M. F. Bobrov, L. S. Kol’tsova, E. A. Karpuzova, M. M. Krayushkin, S. I. Luiksaar, G. V. Popova, A. I. Shienok, N. L. Zaichenko, Valery A. Barachevsky
Publikováno v:
Russian Chemical Bulletin. 59:1353-1359
Comparative spectral kinetic studies of the photochromic properties of a novel N-aminofulgimide and the previously synthesized aminospirooxazine intended for the synthesis of organic-inorganic photochromic systems based on cyclotriphosphazene were pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efdb3163a1f186b8c32633e8682f5036
https://doi.org/10.1007/s11172-010-0246-5
https://doi.org/10.1007/s11172-010-0246-5
Publikováno v:
ARKIVOC, Vol 2001, Iss 9, Pp 49-54 (2002)
Aryldichlorocarbenium tetrachloroaluminates are shown to be preferable reagents for the aroylation of 2-acetylthiophene, while the usual ArCOCl·AlCl3 complexes give better results in aroylation of 3-acetylthiophene. Scope and limitations of both aro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cb1c96b4d4b5f6bbb3fe396e86873c
https://doi.org/10.3998/ark.5550190.0002.908
https://doi.org/10.3998/ark.5550190.0002.908
Publikováno v:
Russian Chemical Bulletin. 49:886-893
The reductive condensation of trichloromethylarenes with hydrazines can proceed without intermediate formation of pyridinium salts and without participation of pyridine in the reduction act. Variants of reductive condensation using hydrazines as redu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a84868feb1cc2854af0cc0bd0c06731
https://doi.org/10.1007/bf02494714
https://doi.org/10.1007/bf02494714
Publikováno v:
Chemistry of Heterocyclic Compounds. 36:1172-1176
The reaction of N-(4-pyridyl)pyridinium and 4-chloropyridinium salts obtained from 1-trichloromethyl-2,4,6-trimethylbenzene and pyridine with N-nucleophiles such as piperidine and morpholine and with C-nucleophiles such as N,N-dimethylaniline and ind
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2d7f74c977706701ece8884f420cb20
https://doi.org/10.1023/a:1002816615941
https://doi.org/10.1023/a:1002816615941
Autor:
Leonid D. Popov, V. A. Kogan, Igor N. Shcherbakov, A. M. Gorelik, Valery A. Barachevsky, S. I. Luiksaar, O. V. Venediktova, M. M. Krayushkin
Publikováno v:
Russian Chemical Bulletin. 58:2423-2425
A Schiff base was synthesized from 5-methoxysalicylaldehyde and N-aminofulgimide, viz., 1-amino-3-[1-(2,5-dimethylthiophen-3-yl)ethylidene]-4-isopropylidenepyrrolidine-2,5-dione. The compound synthesized undergoes photochromic transformations typical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27eca4d4542627fa9368837ea349994d
https://doi.org/10.1007/s11172-009-0338-2
https://doi.org/10.1007/s11172-009-0338-2
Publikováno v:
Chemistry of Heterocyclic Compounds. 35:871-874
2,5-Bis(5-aryl-1,3,4-oxadiazol-2-yl)furans are synthesized via the reaction of trichloromethylarenes with furan-2,5-dicarboxylic acid dihydrazide. The structures of the products are confirmed by IR and mass spectra.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9549ba2d3ae06a0e4315d1648d209227
https://doi.org/10.1007/bf02252115
https://doi.org/10.1007/bf02252115
Publikováno v:
Russian Chemical Bulletin. 47:2238-2245
The reactions of trichloromethylarenes with excess hydrazine hydrate in ethanol gives symmetrical 2,5-diaryl-1,3,4-oxadiazoles in 68–96% yields. The reaction of 1,4-bis(trichloromethyl)benzene with acylhydrazines in an ethanol-pyridine mixture give
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43c2529ff1f2324289dcc207c2986997
https://doi.org/10.1007/bf02494289
https://doi.org/10.1007/bf02494289