Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Ivan Wlassics"'
Publikováno v:
Molecules, Vol 16, Iss 8, Pp 6512-6540 (2011)
In this study we will present and discuss both the synthesis of CF2=CFCF2OSO2F (perfluoroallyl fluorosulfate, FAFS), focusing in particular on the important role of C3F6/SO3 ratio, reaction temperature and boron catalyst/SO3 ratio on FAFS’ yield an
Externí odkaz:
https://doaj.org/article/73ac8ff042db44b4a2cf031b434526b8
Autor:
Pierangelo Metrangolo, Giancarlo Terraneo, Tullio Pilati, Archan Dey, Giuseppe Resnati, Ivan Wlassics
Publikováno v:
Journal of Fluorine Chemistry. 130:816-823
Perfluoroalkyl chains in solids are highly disordered in a wide range of temperatures. Poor attention is typically given to this problem in crystallographic studies to the point that no attempt is frequently made in order to model the collected data
Autor:
Ivan Wlassics, Vito Tortelli
Publikováno v:
Collection of Czechoslovak Chemical Communications. 73:1719-1728
Coupling reactions of chlorofluoro- and perfluoroalkyl iodides Rf-I with Rf = ClCF2CFCl(CF2)3CF2-, ClCF2CFClO(CF2)3CF2-, ClCF2CFCl-, (CF3)2CF- , (CF3)2CFCF2CF2- in the presence of a zinc/solvent system give dimers in good yields. Both homodimerizatio
Autor:
Ivan Wlassics, Vito Tortelli
Publikováno v:
Journal of Fluorine Chemistry. 127:240-248
Carrier mediated telomerization (CMT) between C 2 F 4 and bromochlorofluoroethanes has been evaluated in terms of product distributions arising from CMT and ‘normal’ telomerization. The effect of parameters like type of initiator and telogen, TFE
Autor:
Vito Tortelli, Ivan Wlassics
Publikováno v:
Journal of Fluorine Chemistry. 126:45-51
Perfluoropolyether (PFPE) diacyl halides of formula XCOCF 2 O[(CF 2 O) n (CF 2 CF 2 O) m ] p CF 2 COX, with X = Cl, F and molecular weight (MW) 400–4000 g mol −1 are smoothly converted in high yields to the corresponding α, ω diiodides in the a
Autor:
Ivan Wlassics
Publikováno v:
Journal of Fluorine Chemistry. 125:1519-1528
The second order 2π + 2π homo- and co-dimerization between various classes of fluorinated olefins has been investigated. The fluorinated olefins examined in this study were: (1) Rf OCF CF2 (perfluorinated vinyl ethers); (2) Rf CF CF2 (perfluorinate
Publikováno v:
Journal of Fluorine Chemistry. 123:119-126
In a model study, 1 H, 19 C, 13 C- 1 H and 1 H- 1 H correlated NMR techniques confirm a Markovnikov type reaction intermediate for the major coupling products between a short, low MW perfluorinated iodide C 2 F 5 I ( I ) and a short, low MW fluorinat
Publikováno v:
Journal of Fluorine Chemistry. 121:65-74
This paper deals with the synthesis of perfluoropolyether (PFPE) (poly)diacyl peroxides with mean EWs ranging from 500 to 4000 g eq.−1 via H2O2 and base from the corresponding PFPE diacyl halides, their decomposition (thermal and hydrolytic) and th
Autor:
Cristian Gambarotti, Maurizio Sansotera, Alberto Baggioli, Ivan Wlassics, Walter Navarrini, Francesco Venturini, Raffaella Soave, Antonino Famulari, Stefano Valdo Meille
Publikováno v:
ChemInform. 45
Perfluoroalkyl radicals, generated by thermal decomposition of perfluorodiacyl peroxides, react selectively with quinone rings of 1,4-naphthoquinones. In the presence of a non-conjugated alkene such as 1-hexene, perfluoroalkyl radicals add to the dou
Autor:
Stefano Valdo Meille, Antonino Famulari, Francesco Venturini, Maurizio Sansotera, Walter Navarrini, Cristian Gambarotti, Alberto Baggioli, Raffaella Soave, Ivan Wlassics
Publikováno v:
Tetrahedron (Oxf., Online) 70 (2014): 5298–5309. doi:10.1016/j.tet.2014.05.024
info:cnr-pdr/source/autori:Sansotera M.; Gambarotti C.; Famulari A.; Baggioli A.; Soave R.; Venturini F.; Meille S.V.; Wlassics I.; Navarrini W./titolo:Free-radical selective functionalization of 1,4-naphthoquinones by perfluorodiacyl peroxides/doi:10.1016%2Fj.tet.2014.05.024/rivista:Tetrahedron (Oxf., Online)/anno:2014/pagina_da:5298/pagina_a:5309/intervallo_pagine:5298–5309/volume:70
info:cnr-pdr/source/autori:Sansotera M.; Gambarotti C.; Famulari A.; Baggioli A.; Soave R.; Venturini F.; Meille S.V.; Wlassics I.; Navarrini W./titolo:Free-radical selective functionalization of 1,4-naphthoquinones by perfluorodiacyl peroxides/doi:10.1016%2Fj.tet.2014.05.024/rivista:Tetrahedron (Oxf., Online)/anno:2014/pagina_da:5298/pagina_a:5309/intervallo_pagine:5298–5309/volume:70
Perfluoroalkyl radicals, generated by thermal decomposition of perfluorodiacyl peroxides, react selectively with quinone rings of 1,4-naphthoquinones. In the presence of a non-conjugated alkene such as 1-hexene, perfluoroalkyl radicals add to the dou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::417edb5441af7ec10a74f6509f1c2b47