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Microwave step‐growth polymerization of 5‐(4‐methyl‐2‐phthalimidylpentanoylamino)isophthalic acid with different diisocyanates
Author(s) -
Mallakpour Shadpour,
Dinari Mohammad
Publication year - 2008
Publication title -
polymers for advanced technologies
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.61
H-Index - 90
eISSN - 1099-1581
pISSN - 1042-7147
DOI - 10.1002/pat.1142
Subject(s) - isophthalic acid , polymerization , polymer chemistry , specific rotation , materials science , polyamide , monomer , condensation polymer , phthalic anhydride , thionyl chloride , triphenyl phosphite , trimesic acid , thermal stability , catalysis , polymer , terephthalic acid , organic chemistry , chloride , chemistry , polyester , molecule , metallurgy , composite material
The utilization of microwave energy in polymer synthesis is a fast growing field of research leading to a more rapid and cleaner polymerization process. In order to synthesize novel optically active monomer 5‐(4‐methyl‐2‐phthalimidylpentanoylamino)isophthalic acid ( 6 ), the reaction of phthalic anhydride with l ‐leucine was carried out in an acetic acid solution and 4‐methyl‐2‐phthalimidylpentanoic acid as an imide acid was obtained in good yield. Then, it was converted to 4‐methyl‐2‐phthalimidylpentanoyl chloride by treatment with thionyl chloride. This acid chloride was reacted with 5‐aminoisophthalic acid and the novel bulky aromatic amide‐imide chiral monomer 6 was obtained in high yield and was characterized with spectroscopy techniques as well as specific rotation and elemental analysis. Polycondensation of monomer 6 with different diisocyanates such as 4,4′‐methylenebis(phenyl isocyanate), toluene‐2,4‐diisocyanate, isophorone diisocyanate, and hexamethylene diisocyanate was performed by two different methods: microwave irradiation and classical heating polymerization techniques in the presence of various catalysts and without a catalyst. The microwave polymerization technique provides a new way for the production of polymers at high rates. The resulting novel optically active polyamides have inherent viscosities in the range of 0.25–0.63 dl/g. They show good thermal stability and are soluble in amide‐type solvents. The obtained polyamides were characterized by FT‐IR, 1 H‐NMR spectroscopy, elemental analyses, specific rotation, and thermal analyses methods. Copyright © 2008 John Wiley & Sons, Ltd.