1964
DOI: 10.1021/ac60217a036
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Determining Structure of Paraffinic Chains by NMR.

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Cited by 46 publications
(11 citation statements)
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“…This absorption is at slightly higher field than that for the geminal dirnethyl groups in cationic 1,3-poly(4-rnethyl-l-pentene) (7) which is found a t 0.82 ppm. The peak a t 0.88 pprn represents the center of a triplet arising from the methyl group in the ethyl s i d e chain, its chemical shift is in excellent agreement with the expected value (8). The broadened and slightly split peak at 1.18 ppm represents the 3 methylene groups i n the backbone, apparently somewhat nonequivalent because of the different substituents on the quarternary carbon.…”
supporting
confidence: 71%
“…This absorption is at slightly higher field than that for the geminal dirnethyl groups in cationic 1,3-poly(4-rnethyl-l-pentene) (7) which is found a t 0.82 ppm. The peak a t 0.88 pprn represents the center of a triplet arising from the methyl group in the ethyl s i d e chain, its chemical shift is in excellent agreement with the expected value (8). The broadened and slightly split peak at 1.18 ppm represents the 3 methylene groups i n the backbone, apparently somewhat nonequivalent because of the different substituents on the quarternary carbon.…”
supporting
confidence: 71%
“…As for aliphatic protons, H α and H β are dominant for two extracts, suggesting the existence of branched alkyl side chains in the α- and β-position to the aromatic rings, such as methyl, methylene, and/or methine. In addition, two samples show multiple peaks in 1.0–2.0 ppm, indicating the existence of both paraffinic and naphthenic methylene structures . Additionally, a weak peak can be observed at 5.7 ppm, indicating that there exist some phenolic-containing species in E CYC .…”
Section: Resultsmentioning
confidence: 94%
“…In addition, two samples show multiple peaks in 1.0−2.0 ppm, indicating the existence of both paraffinic and naphthenic methylene structures. 51 Additionally, a weak peak can be observed at 5.7 ppm, indicating that there exist some phenolic-containing species in E CYC . The above results suggest that more organic matters can be extracted by CYC than THF during MAE process.…”
Section: Energy and Fuelsmentioning
confidence: 99%
“…53) shows a broad component with a distance between the extrema greater than 15 OeD When the film is turned along the field, for a considerable part of the CH 2 groups e ~ 90° and the line narrows. In oriented polyethylene fiber a change has been observed in the form of the line in relation to the angle between the fiber and the field vector (see page 168).…”
Section: Nuclear Magnetic Resonance In Oriented Polymersmentioning
confidence: 99%