Zobrazeno 1 - 10
of 108
pro vyhledávání: '"G. G. FURIN"'
Publikováno v:
Russian Journal of Applied Chemistry. 80:405-418
Perfluoroolefins react with isopropyl alcohol under the conditions of radical initiation to form partially fluorinated aliphatic alcohols. The reactions of these alcohols with hexafluoropropylene and compounds containing labile halogen atoms (in part
Autor:
K. I. Tugashov, A.P. Zaraisky, G. G. Furin, Pavel V. Petrovskii, I. A. Tikhonova, A.A. Yakovenko, F. M. Dolgushin, Vladimir B. Shur
Publikováno v:
Journal of Organometallic Chemistry. 692:953-962
Cyclic trimeric perfluoro- o -phenylenemercury ( o -C 6 F 4 Hg) 3 ( 1 ) is capable of reacting with nitromethane to give complex {[( o -C 6 F 4 Hg) 3 ](CH 3 NO 2 )} ( 2 ) containing one molecule of the nitro compound per one macrocycle molecule. In t
Autor:
G. G. Furin, Vladimir B. Shur, B.N. Strunin, F. M. Dolgushin, A.A. Yakovenko, K. I. Tugashov, Pavel V. Petrovskii, I. A. Tikhonova
Publikováno v:
Inorganica Chimica Acta. 359:2728-2735
The interaction of cyclic trimeric perfluoro-o-phenylenemercury (o-C6F4Hg)3 (1) with azulene results in the formation of a complex, {[(o-C6F4Hg)3](azulene)} (2), containing one molecule of azulene per one macrocycle molecule. The complex represents a
Autor:
O. I. Kachurin, Vladimir B. Shur, G. G. Furin, I. A. Tikhonova, L. I. Velichko, A.P. Zaraisky
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 231:103-111
Cyclic trimeric perfluoro-o-phenylenemercury (o-C6F4Hg)3 (1) exhibits a high catalytic activity in the phase transfer nitration of various aromatic substrates (2-methylnaphthalene, 1,3- and 2,6-dimethylnaphthalenes, acenaphthene, anthracene, pyrene)
Autor:
G. G. Furin, E. L. Zhuzhgov
Publikováno v:
Russian Journal of General Chemistry. 74:1534-1537
The reaction of perfluoro-5-azanon-4-ene with KSCN in an aprotic dipolar solvent provides perfluoro-1-(butylimino)butyl isothiocyanate. The latter was reacted with n-propylamine in the presence of triethylamine to obtain fluoro-substituted derivative
Publikováno v:
Russian Journal of Applied Chemistry. 77:98-101
A procedure was developed for preparing partially fluorinated dialkyl ethers by the reaction of hexafluoropropylene with aliphatic and polyfluorinated alcohols in the presence of KOH. On treatment with concentrated sulfuric acid, these ethers form al
Autor:
M. Yu. Antipin, O.G. Ellert, K. I. Tugashov, I. A. Tikhonova, F. M. Dolgushin, Vladimir M. Novotortsev, G. G. Furin, Vladimir B. Shur
Publikováno v:
Journal of Organometallic Chemistry. 689:82-87
Cyclic trimeric perfluoro-o-phenylenemercury (o-C6F4Hg)3 (1) is able to bind hexacyanoferrate(III) and nitroprusside anions to form complexes {[(o-C6F4Hg)3]2[Fe(CN)6]}3− and {[(o-C6F4Hg)3]2[Fe(CN)5NO]}2−, respectively, which contain one anionic s
Autor:
K. I. Tugashov, Lylia N. Teplitskaya, Vladimir B. Shur, Fedor M. Dolgushin, Pavel V. Petrovskii, Igor B. Sivaev, I. A. Tikhonova, Lina M. Epstein, Andrey M. Filin, G. G. Furin, Elena S. Shubina, Vladimir I. Bregadze
Publikováno v:
Russian Chemical Bulletin. 52:594-600
The reaction of cyclic trimeric perfluoro-o-phenylenemercury (o-C6F4Hg)3 (1) with the polyhedral [B12H11SCN]2– anion in THF at 20 °C affords the {[(o-C6F4Hg)3](B12H11SCN)}2– (4) and {[(o-C6F4Hg)3]2(B12H11SCN)}2– (5) complexes. Complex 5 was is
Autor:
Vladimir B. Shur, F. M. Dolgushin, Pavel V. Petrovskii, I. A. Tikhonova, K. I. Tugashov, G. G. Furin
Publikováno v:
Journal of Organometallic Chemistry. 654:123-131
Cyclic trimeric perfluoro- o -phenylenemercury ( o -C 6 F 4 Hg) 3 ( I ) readily reacts with N , N -dimethylformamide and hexamethylphosphoramide to form complexes {[( o -C 6 F 4 Hg) 3 ](HCONMe 2 ) 2 } ( II ) and {[( o -C 6 F 4 Hg) 3 ][(Me 2 N) 3 PO]
Autor:
G. G. Furin, A. V. Rogoza
Publikováno v:
Russian Journal of General Chemistry. 72:957-962
The reactions of perfluoro-3-isothiocyanato-2-methyl-2-pentene with PPh3 and P(NEt2)3 in the presence of NaBF4, KI, and NaBPh4 form phosphonium salts with the heterocyclic substituent (4E)-5,5-bis(trifluoromethyl)-4-(tetrafluoroethylidene)-4,5-dihydr