The polymers were synthesized by the solution polycondensation method at low temperature, in high yields and moderate to high inherent viscosities.
The hydroxyl groups of the tartaric acid derivatives were first protected and the polyesters were synthesized by bulk and solution polycondensation methods.
Prepolymers prepared by solution polycondensation were cast and successively post-polymerized to form a network.
A series of new polyesters containing the hexafluoro-2-propoxy group was synthesized by solution polycondensation.
Polythioamides were prepared by solution polycondensation at low temperature, in high yields and moderate to high inherent viscosities.
A series of liquid crystalline copolyesters, possibly having auxetic behaviour, were designed and synthesized by solution polycondensation from 4,4′- decanoxy) dibenzoyl chloride with 2,5-bis(p-alkoxy benzoyloxy) hydroquinone and 4,4′- decanoxy-α,ω-dibenzoyldechloridedifferent ratios.
The poly azomethine ether)s were prepared by solution polycondensation using 4,4′-diformyl-α,ω-diphenoxydecane, 4,4′-diformyl-3,3-methoxy-α,ω-diphenoxydecane with various diamines.
Polymer electrolytes were synthesized by solution polycondensation of 4-chlorophenyldichlorophosphonate as a linking agent and PEG with different molecular weights (MW of 200 and 2000).
A series of aromatic polyamides nanoparticles with pendant structures comprised of m- and p-acetoxybenzamide groups were synthesized by solution polycondensation of 5- 4-acetoxybenzamido)isophthaloyl chloride or 5- 4-acetoxybenzamido)isophthaloyl chloride with commercially available aromatic diamines.
The hydrazide polymers 31 and 32 were efficiently prepared in quantitative yields by solution polycondensation of the bis-hydrazides 28 and 29, respectively, with the readily available isopthaloyl chloride 30 [19–22] in N,N-dimethylacetamide.
