Abstract:
:An aromatic chiral diacid monomer, 5-[4-(2-phthalimidiylpropanoylamino)-benzoylamino]isophthalic acid was synthesized in five steps under conventional heating in high yield and purity. A series of soluble, thermally stable and optically active polyamides (PA)s containing pendent groups made of phthalimide, flexible L: -alanine and benzamide sequence have been successfully synthesized under microwave irradiation. Excellent yields and very short reaction time were the main characteristics of this method. The same polymerization reactions were also carried out by conventional thermal heating and the results are compared. The resulting PAs had inherent viscosity in the range of 0.50-0.79 dL g(-1). All of the these polymers are readily dissolved in various solvents such as N-methyl-2-pyrrolidinone, N,N-dimethylacetamide and N,N-dimethylformamide and showed glass-transition temperature above 200 degrees C. Thermogravimetric analysis demonstrated that the 10% weight-loss temperatures in nitrogen were 372 and 422 degrees C for selected two PAs. All of these polymers showed optical rotation which is due to successful insertion of L: -alanine in the structure of chiral diacid monomer.
journal_name
Amino Acidsjournal_title
Amino acidsauthors
Mallakpour S,Rafiee Zdoi
10.1007/s00726-008-0186-7subject
Has Abstractpub_date
2009-10-01 00:00:00pages
665-72issue
4eissn
0939-4451issn
1438-2199journal_volume
37pub_type
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