''Criss-cross''-cycloaddition of 4,4'-diisocyanatodiphenyl ether and 4
-methoxybenzaldazine was used to synthesize alpha,omega-diisocyanato t
elechelics of molecular weights between 1600 and 3900. These precursor
s were reacted with different alpha,omega-dihydroxy functionalized ali
phatic polyethers to produce segmented block copolymers in which the p
recursors obtained by cycloaddition reaction provide hard segment doma
ins embedded in a polyether soft segment matrix. The resulting materia
ls were soluble in common organic solvents such as tetrahydrofuran and
chloroform and were characterized by spectroscopic techniques (H-1-,
C-13 NMR, IR spectroscopy) as well as gel permeation chromatography (G
PC) for molar mass determination The block copolymers were molded in a
hot stage press, and the resulting samples were characterized by diff
erential scanning calorimetry (DSC), dynamic mechanical thermal analys
is (DMTA) and stress-strain measurement. The materials with a hard seg
ment fraction below 0.36 and a molecular weight above (M) over bar(n)
= 90 000 were elastomers with ultimate elongations above 700%.