Poly(2-oxazoline)s (POZs) are widely investigated for
their applications
in various fields due to their unique properties. To exploit and combine
different characteristics of the POZ family, 2-oxazoline monomers
can be copolymerized to prepare tailor-made copolymers with the desired
glass transition temperature (T
g), melting
temperature (T
m), amphiphilicity, and
functionality. Here, we report the synthesis and characterization
of 2-oxazoline monomers and a range of POZ copolymers produced, thereof.
2-Propyl-2-oxazoline (PrOZ) and 2-pentyl-2-oxazoline (PeOZ) monomers
were synthesized by two different methods starting from nitriles or
carboxylic acids. A number of POZ copolymers were synthesized by copolymerization
of 2-ethyl-2-oxazoline (EOZ) with either one of PrOZ, PeOZ, or 2-phenyl-2-oxazoline
(PhOZ) at three different compositions (25:75, 50:50, and 75:25) and
three molecular weights (1000, 2000, and 5000 Da). The successful
synthesis of the monomers and copolymers was demonstrated through
their structural analysis by 1H NMR and FTIR. SEC results
confirmed the targeted molar masses of the copolymers and living nature
of the polymerization by showing low dispersity values. Thermal properties
of the copolymers were studied using DSC and TGA. DSC studies revealed
the amorph and random state of the copolymers with obtained T
g values for the copolymers in the range of
−3 to 84 °C depending on their molecular weight and type
of the side chain. While the presence of longer aliphatic side chains
resulted in lower T
g values, the presence
of 2-phenyl substituents on the polymer led to higher T
g values. The decomposition temperatures determined by
TGA were in the range of 328 to 383 °C depending on the molecular
weight, composition, and side chain of the copolymers. It was observed
that higher molecular weights led to higher T
g values and decomposition temperatures. While copolymers with
aliphatic side chains exhibited a single-step decomposition profile,
the decomposition of copolymers having aromatic side chains occurred
in multiple steps. The variations in the molecular weight, composition,
and side chains of the copolymers resulted in a library of tailorable
amphiphilic copolymers suitable for multiple applications ranging
from biomedical applications to composite manufacturing.