Different methods of synthesis involved in the preparation of fluorinated t
elechelics (or alpha,w-difunctional compounds) from alpha,w-diiodoperfluoro
alkanes for obtaining well-defined fluoropolymers are described. This revie
w focuses on molecules in which fluorinated chains are located on the backb
one and not in a lateral position. First, a bibliographical approach develo
ps the syntheses of alpha,w-diiodoperfluoroalkanes (1) either by chemical t
ransformations of telechelic derivatives or by telomerisation of fluoroolef
ins with molecular iodine or diiodoperfluoroalkanes. Then, fluorotelechelic
s are synthesised by means of four different processes: (a) by the chemical
change in the presence of metalic salts: Cb) from the bismonoaddition of 1
to w-functional unsaturated derivatives; (c) from the bis(monoethylenation
) of 1 followed by difunctionalisation (e.g., nucleophilic substitution); (
d) from the coupling reactions between 1 and alpha-iodo-w-functional reacta
nts. Finally, this review describes how several well-defined fluoropolymers
can be produced from these fluorinated telechelics. Their specific chemica
l, physical and thermal properties are discussed with regard to modern indu
strial requirements. (C) 1999 Elsevier Science S.A. All rights reserved.