2,2-Dibutyl-2-stanna-1,3-dioxacycloalkanes were used as cyclic initiat
ors for the ring-opening polymerization of various lactons. This metho
d exclusively yielded series of macrocyclic polylactones without any c
ompetition with linear polymers. Under optimized reaction conditions t
hese macrocyclic polymerizations obey the pattern of ''living polymeri
zations''. The living chain ends allow the syntheses of macrocyclic bl
ockcopolymers. The macrocyclic polylactones react with carboxylic acid
chlorides by ring-opening yielding telechelic oligo or polylactones.
Furthermore, the tin containing macrocyclic polylactones can be used a
s difunctional ''monomers'' for polycondensations with dicarboxylic ac
id dichlorides.