1998
DOI: 10.1016/s0022-1139(98)00142-0
|View full text |Cite
|
Sign up to set email alerts
|

Synthesis and polymerization of fluorinated monomers bearing a reactive lateral group Part 2. Synthesis of nonconjugated dienes

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
4
0

Year Published

1999
1999
2013
2013

Publication Types

Select...
7
1

Relationship

0
8

Authors

Journals

citations
Cited by 16 publications
(4 citation statements)
references
References 24 publications
0
4
0
Order By: Relevance
“…The other assignments have been deduced from the chemical shifts corresponding to the characteristic CF 27 This latter compound was prepared by the radical addition of C 6 F 13 -CH 2 CF 2 I to FAc. 27 For the calculation of the amounts of both comonomeric units in the copolymer, the integrations of the signals in the three zones above are noted I 4 , I 5 and I 6 , respectively.…”
Section: Resultsmentioning
confidence: 99%
“…The other assignments have been deduced from the chemical shifts corresponding to the characteristic CF 27 This latter compound was prepared by the radical addition of C 6 F 13 -CH 2 CF 2 I to FAc. 27 For the calculation of the amounts of both comonomeric units in the copolymer, the integrations of the signals in the three zones above are noted I 4 , I 5 and I 6 , respectively.…”
Section: Resultsmentioning
confidence: 99%
“…The synthesis of the monomers was reported in the same patent, while the optimization of F 2 CdCF(CH 2 ) n OR (where n ) 1 or 3 and R ) H or Ac) was later on extensively described. 256 Other functional trifluorovinyl monomers have also been prepared, bearing either an ω-insaturation [257][258][259] or a carboxylic, 260,261 a nitrile, 262 an amide, 258 a sultone, 257 an epoxide, 263 a hydroxyl, 255,256,260,264 or a thioacetoxy group. 265,266 More exotic routes to trifluorovinyl end groups in metallic complexes have also been reviewed.…”
Section: Poly(vdf-co-functional Perfluorovinyl Monomer) Copolymersmentioning
confidence: 99%
“…The synthesis of the monomers was reported in the same patent, while the optimization of F 2 CCF(CH 2 ) n OR (where n = 1 or 3 and R = H or Ac) was later on extensively described . Other functional trifluorovinyl monomers have also been prepared, bearing either an ω-insaturation or a carboxylic, , a nitrile, an amide, a sultone, an epoxide, a hydroxyl, ,,, or a thioacetoxy group. , More exotic routes to trifluorovinyl end groups in metallic complexes have also been reviewed . Radical copolymerizations of VDF with F 2 CCF(CH 2 ) 3 OR , (according to the nature and the amount of the functional monomer, the T g values ranged from −23 to −8 °C) or with F 2 CCF(CH 2 ) 3 SCOR , have been investigated, leading to original elastomers .…”
Section: Copolymerization Of Vinylidene Fluoridementioning
confidence: 99%
“…The radical addition of iodine monochloride onto CTFE has been extensively investigated. , The resulting 1,2-dichloro-2-iodotrifluoroethane was used to prepare various trifluorovinyl monomers bearing functional side groups as described in Scheme . This enabled, for example, the cross-linking of polymers. , …”
Section: Synthesis and Homopolymerization Of Chlorotrifluoroethylenementioning
confidence: 99%