4.5 Article

Synthesis and characterization of novel optically active poly(imide-urethane)s derived from N,N′-(pyromellitoyl)-bis-(L-leucine) diisocyanate and aromatic diols

Journal

POLYMER INTERNATIONAL
Volume 53, Issue 2, Pages 184-190

Publisher

WILEY
DOI: 10.1002/pi.1416

Keywords

N,N '-(pyromellitoyl)-bis-(L-leucine) diacylazide; poly(imide-urethane)s; optically active polymers; inherent viscosities; thermally stable polymers; diisocyanate

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N,N'-(Pyromellitoyl)-bis-(L-leucine) diacid was reacted with ethyl chloroformate in the presence of triethylamine followed by reaction with activated sodium azide and gave N,N'-(pyromellitoyl)-bis-(L-leucine) diacylazide in high yield. This diacylazide was heated in dry benzene and gave the unstable N,N'-(pyromellitoyl)-bis-(L-leucine) diisocyanate (5) in quantitative yield. Thus, diisocyanate 5 was generated in situ and polycondensation reaction of this monomer with several aromatic diols, such as 4,4'-dihydroxybiphenyl, 1,4-hydroquinone, bisphenol A, phenolphthalein and 1,4-dihydroxyanthraquinone, was performed in dry toluene under refluxing in the presence of 1,4-diazabicyclo[2.2.2]octane (triethylenediamine) as a catalyst. The polymerization reactions proceeded within 48 h, producing a series of optically active poly(imide-urethane)s with good yield and moderate inherent viscosity in the range 0.18-0.28 dl g(-1). All of the above polymers were fully characterized by infrared spectra, elemental analyses and specific rotation. Some structural characterization and physical properties of these optically active poly(imide-urethane)s are reported (C) 2003 Society of Chemical Industry.

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