Hr. Stapert et al., SYNTHESIS AND CHARACTERIZATION OF ALIPHATIC POLY(ESTER-AMIDE)S CONTAINING SYMMETRICAL BISAMIDE BLOCKS, Macromolecular symposia, 130, 1998, pp. 91-102
A series of symmetrical diols were synthesised through ring-opening of
lactones with different ring sizes by alkane diamines in moderate to
good yields. Ring-opening of the dilactones glycolide and lactide with
a diamine in equimolar amounts afforded symmetrical diols in quantita
tive yield. Aliphatic poly(ester-amide)s were prepared by polycondensa
tion of N,N'-bis(caproyl)butane diamide, dimethyl adipate and 1,4-buta
nediol. The structure of the diamide was retained in the polymer. The
polymers synthesized are semi-crystalline materials that possess order
ed structures in the solid phase over almost the entire copolymer rang
e. Depending on thermal history and copolymer composition thermal anal
yses is in agreement with the presence of pseudo-hexagonal crystal str
uctures below 75 degrees C, a fast melting recrystallization at this t
emperature and a triclinic structure at higher temperatures.