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Characterization of aromatic polymers (benzenoid and heterocyclic) by cross-polarization, magic-angle 13C-NMR spectroscopy

✍ Scribed by Brown, Charles Eric ;Khoury, Issam ;Bezoari, Massimo D. ;Kovacic, Peter


Book ID
105333935
Publisher
John Wiley and Sons
Year
1982
Weight
593 KB
Volume
20
Category
Article
ISSN
0360-6376

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✦ Synopsis


Abstract

The cross‐polarization, magic‐angle ^13^C‐NMR spectra of solid samples of poly(p‐phenylene), its nitro derivative, polymerized biphenyl, poly(p‐phenylene sulfide), poly(1‐methyl‐2,5‐pyrrolylene), poly(1‐phenyl‐2,5‐pyrrolylene), poly(2,5‐thienylene), and poly(2,5‐selenienylene) and the high‐resolution ^13^C‐NMR spectrum of poly(m‐phenylene) in solution are presented and assigned. In all cases the chemical shifts are similar to those of model compounds in solution. In most instances the resonances of the nonprotonated carbon atoms in the solid polymers are more intense than those of the protonated carbons and appear to depend on the charge distribution in the molecular orbitals.


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Structural study of amylose polymorphs b
✍ Fumitaka Horn; Hiroyuki Yamamoto; Asako Hirai; Ryozo Kitamaru 📂 Article 📅 1987 🏛 Elsevier Science 🌐 English ⚖ 827 KB

C.p.-m.a.s. 13C-n.m.r. spectra and 13C spin-lattice relaxation times (I;) at room temperature have been measured for recrystallized samples of different polymorphs of amylose. Although the spectra of A-and B-amyloses in the dry state are very broad and ahnost structureless, the respective resonance