In the present work, several novel optically active nanostructure poly(amide–imide)s (PAI)s were synthesized via step-growth polymerization reaction of chiral diacids based on pyromellitic dianhydride-derived dicarboxylic acids containing different natural am
In the present investigation, a new optically active poly(amide–imide) (PAI) was synthesized from the polymerization reaction of N-trimellitylimido-L-isoleucine diacid with 4,4′-methylenebis(3-chloro-2,6-diethylaniline) using molten tetra-n-butylammonium bro
In this study, Cloisite Na+ was modified with protonated L-phenylalanine (Phe) amino acid as a bioactive molecule via ion-exchange reaction.
Polymer/layered-silicate hybrids nanocomposites have attracted strong interest in today's materials research, as it is possible to achieve impressive enhancements of material properties compared to the pure polymers.
A temperature-sensitive hydrogel was successfully grafted on the surface of non-woven poly(propylene) materials.
Bionanocomposites (BNCs) containing 4, 8 and 12% (w/w) modified ZnO nanoparticles (NPs) were successfully prepared by homogenous dispersion of these NPs in an optically active poly(amide-imide) (PAI) matrix through an ultrasonic process. PAI was synthesized via solution polycondensation of 3,5-diamino-N-(4-hydroxyphenyl) benzamide and N,N-(pyromellitoyl)-bis-L-phenylalanine diacid chloride at low temperature.
Polyimide–silica nanocomposites are attractive hybrid architectures that possess excellent mechanical, thermal and chemical properties.
This reports a successful approach to chiral synthetic poly(amide-imide)s by condensation polymerization reaction of chiral diacids N-trimellitylimido-S-valine, N-trimellitylimido-L-leucine, N-trimellitylimido-L-alanine, and N-trimellitylimido-L-isoleucine with 5-(2-benzi
For the first time, acidic monomer chiral N-acryloyl-L-phenylalanine was polymerized directly by atom transfer radical polymerization under mild conditions.