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NMR-based structural characterization of common aromatic poly(amic acid) polymers    
Yazarlar
Doç. Dr. İdris YAZGAN
Kastamonu Üniversitesi, Türkiye
Özet
Polyamic acid (PAA) has been widely synthesized as the precursor of polyimide for over 50 years. PAA has had recent attention when used as a final polymer in a variety of applications including sensors, flexible electronics, drug delivery and food packaging. In all cases, structural modifications are sought to advance usability of PAA polymers, where chemistry of the polymers plays a key role for further modifications. However, there is a gap in literature that would discuss structural and cis-/trans-isometric characterizations of the PAA polymers. In this study, common PAA polymers synthesized from the couples of (1) pyromellitic dianhydride and 4,4′-oxydianiline, (2) pyromellitic dianhydride-4-sulfonyldianiline, (3) 4,4′-carbonyldiphtalic dianhydride and 4,4′-oxydianiline and (4) pyromellitic dianhydride and 4,4′-ethylenedianiline were characterized with 1D and 2D NMR and supported with ATR-FTIR techniques. The findings revealed that both diamine and dianhydride sources along with the solvent choice are crucial for cis-/trans-binding of diamine to dianhydride monomers, average molecular weight and intramolecular interactions. The current study, to the best of our knowledge, is the first report on structural annotation of common PAA polymers along with the effect of the solvent on the isomers and average molecular weight.
Anahtar Kelimeler
IR | Isomerization | Monomer | NMR | Polyamic acid
Makale Türü Özgün Makale
Makale Alt Türü SSCI, AHCI, SCI, SCI-Exp dergilerinde yayımlanan tam makale
Dergi Adı Polymer Bulletin
Dergi ISSN 0170-0839
Dergi Tarandığı Indeksler SCI
Makale Dili İngilizce
Basım Tarihi 04-2019
Sayfalar 1 / 13
Doi Numarası 10.1007/s00289-019-02793-0
Makale Linki http://link.springer.com/10.1007/s00289-019-02793-0
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
SCOPUS 5
NMR-based structural characterization of common aromatic poly(amic acid) polymers

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