Synthesis and characterization of new optically active poly(amide-imide-urethane) thermoplastic elastomers, derived from 4,4?-(hexafluoroisopropylidene)-N,N?-bis(phthaloyl-L-leucine-p-aminobenzoic acid) and PEG-MDI

2003 ◽  
Vol 91 (4) ◽  
pp. 2288-2294 ◽  
Author(s):  
Shadpour Mallakpour ◽  
Sepideh Khoee
e-Polymers ◽  
2008 ◽  
Vol 8 (1) ◽  
Author(s):  
Abdol Reza Hajipour ◽  
Saeed Zahmatkesh ◽  
Arnold E. Ruoho

AbstractThis Paper deals with the polycondensation between a chiral diacyl chloride (2-(N,N’-pyromelliticdiimido)-bis-propanoic acid chloride (4)) and polyethyleneglycol-diol (PEG-200) and/or three synthetic aromatic diols. The corresponding new PEIs and Co-PEIs which have been obtained in quantitative yields are soluble in polar aprotic solvents, have good thermal stability and optical activity.


e-Polymers ◽  
2009 ◽  
Vol 9 (1) ◽  
Author(s):  
Saeed Zahmatkesh ◽  
Abdol Reza Hajipour

AbstractPyromellitic dianhydride (1) was reacted with L-leucine (2) to result in [N,N'-(pyromellitoyl)-bis-L-leucine diacid] (3). This compound (3) was converted to N,N'-(pyromellitoyl)-bis-L-leucine diacid chloride (4) by reaction with thionyl chloride. The microwave-assisted polycondensation of this diacid chloride (4) with polyethyleneglycol-diol (PEG-200) and/or three synthetic bisphenols furnish a series of new PEIs and Co-PEIs in a laboratory microwave oven (Milestone). The resulting polymers and copolymers have inherent viscosities in the range of 0.31- 0.53 dl g-1. These polymers are optically active, thermally stable and soluble in polar aprotic solvents such as DMF, DMSO, NMP, DMAc and sulfuric acid. All of the above polymers were fully characterized by IR spectroscopy, 1H NMR spectroscopy, elemental analyses, specific rotation and thermal analyses. Some structural characterizations and physical properties of these optically active PEIs and Co-PEIs are reported.


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