Molecular behavior of coronene, pyrene, and hexamethylbenzene blended in a carbonaceous mesophase was investigated by fused state '?C-NMR. Sharp signals attributed to aromatic carbons of these compounds in the fused mesophase pitch were observed at markedly lower fields compared with those in soluti
A two-dimensional 13C-NMR study of powdered and oriented mesophase pitches
β Scribed by M.-L. Hsu; D.M. Grant; R.J. Pugmire; Y. Korai; S.H. Yoon; I. Mochida
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- English
- Weight
- 997 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0008-6223
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β¦ Synopsis
A two-dimensional
13C-NMR chemical-shift-chemical-shift exchange experiment is described which permits the measurement of solid state 13C resonance frequencies at two different sample orientations.
This technique provides a method for probing the principal values of multiple 13C chemical shift tensors in overlapping powder patterns as well as the orientational distribution function in partially oriented materials. Two mesophase pitches derived catalytically from naphthalene and methyl naphthalene have been examined. These two pitches have similar chemical shift tensors for the aromatic carbons indicating that they have similar carbon structural units. However, significant differences in the molecular structure of these two pitches are also noted. The aromatic rings in both oriented pitches exhibit axial ordering with the preferential orientation along the draw axis. The probability of finding the aromatic ring along the draw direction in the oriented mesophase pitch of methyl naphthalene is approximately three times greater than that in the oriented mesophase pitch of the naphthalene sample.
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