Synthesis, characterization, and electrospinning of novel polyaniline–peptide polymers. (September 2016)

• Record Type: Journal Article
• Authors: Archibong, Edikan; Foster, Alexander; Caldwell, Keirsten; Lita, Adrian; Mochona, Bereket; Mateeva, Nelly
• Is Part Of: Applied materials today. Volume 4(2016)
• Page Start: 78
• Page End: 82
• Publication Date: 2016-09
• Subjects: Polyaniline -- Peptides -- Polymerization -- Electrospinning; Materials science -- Periodicals; Materials -- Research -- Periodicals; 620.1105
• DOI: 10.1016/j.apmt.2016.07.004
• Languages: English
• ISSNs: 2352-9407

Abstract

Highlights: Aniline–peptide mixtures were co-polymerized by chemical and electrochemical means. PANI-FLDQV polymer was electrospun with gelatin as a supporting polymer. Preliminary data are promising for extraction of chlorinated toxins. Abstract: Aniline–peptide (FLDQV, FLDQVC, Dansyl-FLDQV, Dansyl-FLDQVC, and FLDQV-AMC) mixtures underwent oxidative chemical and electrochemical polymerization in excess of aniline. The products of the chemical polymerization were low molecular weight polymers containing more than 70% peptide. Electrochemically polymerized species polyaniline-FLDQV (PANI-FLDQV) consisted mainly of polyaniline units containing about 10% peptide. The solubility of the latter in 1, 1, 1, 3, 3, 3-hexafluoro-2-propanol (HFP) was similar to the camphorsulfonic acid (CSA) doped emeraldine base (PANI-CSA) solubility, however the weight composition of the electrospun fibers produced from the two polymers was significantly different. 2D 1 H– 13 C HSQC analyses were employed to analyze the binding between the aniline and peptide moieties. Binding of peptide to polyaniline is reflected by the appearance of extra cross-peaks which display line broadening between the free polyaniline and the free pentapeptide. Peptides may be chemically bonded to the polymer molecules, but they may also act as doping agents to the nitrogen atoms via hydrogen bonding.