684
Views
5
CrossRef citations to date
0
Altmetric
Article

Synthesis and characterization of new poly(amide-imide)s based on [N,N′-(4,4′-carbonyldiphtaloyl)-bis-L-amino diacid]s and dibenzalacetone moieties in the main chain

, &
Pages 523-532 | Published online: 30 May 2012
 

Abstract

Six dicarboxylic acids 3a–f were synthesized by the reaction of 3,3′,4,4′-benzophenonetetracarboxylic dianhydride 1 with L-aminoacids 2a–f in a solution of glacial acetic acid/pyridine (Py) at refluxing temperature. Then six new poly(amide-imide)s PAIs were synthesized by direct polycondensation reaction of [N,N′-(4,4′-carbonyldiphtaloyl)-bis-L-amino diacid]s with 2,5-bis(4-aminobenzilidene)cyclopentanone. Due to the presence of dibenzalacetone moiety in the polymer chain, the PAIs have photosensitive properties. Also these PAIs are optically active and soluble in various organic solvents. These resulting new polymers can be used in column chromatography for the separation of enantiomeric mixtures. The resulted polymers were fully characterized by means of FTIR, 1H NMR spectroscopy, elemental analyses, inherent viscosity, solubility tests, UV–vis spectroscopy, thermogravimetric analysis, and derivative of thermogravimetric.

Notes

aMeasured at a concentration of 0.5 g /dL in DMF at 25 °C.

aMeasured at a concentration of 0.5 g /dL in DMF at 25 °C.

aTemperature at which 5% or 10% weight loss was recorded by TGA at a heating rate of 10 °C/min under N2.

bWeight percentage of material left after TGA analysis at a maximum temperature of 800 °C under N2.

cLimiting Oxygen Index.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.