13C n.m.r. spectral editing techniques have been used to determine the concentrations of aliphatic CH, CH2 and CH, groups directly in aromatic fractions from a North Sea waxy heavy distillate (vacuum gas oil) and a hydrotreated sample of this distillate. To help resolve effective and poor hydrogen-d
N.m.r. characterization of functional groups: 5—on the nature of olefinic end groups in polyisobutylenes
✍ Scribed by Stanley L. Manatt; John D. Ingham; Joseph A. Miller Jr
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 489 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Proton n.m.r. signals for two types of olefinic end groups, -CH,C(CH3)=CH2 (84.68 and 84.87) and -CH=C(CH,), (85.21), have been observed in high molecular weight polyisobutylenes. Comparable amounts of both these end groups exist in commercial and laboratory prepared samples of polyisobutylenes contrary to previous reports that the former group is by far predominant. That different catalysts produce different relative concentrations of these end groups is demonstrated. Evidence for the presence of a third type of unsaturation from the -CH,C(=CH,)CH,structure is discussed.
📜 SIMILAR VOLUMES
## Abstract Linear correlation coefficients were obtained for the substituent effect of the nitro group in primary nitroalkanes. The solvent effect of chloroform is also discussed, as well as the influence of the scalar relaxation on the half‐width of α‐carbons in ^13^C n.m.r. spectroscopy.
The constants of thermolysis rate of C,H,~(CH,),~O~(CH,),-C6HS ethers were measured in conditions close to those of coal liquefaction (hydrogen pressure of 8.5 MPa; temperature up to 410°C) but minimizing secondary conversions (i.e. in ten-fold excess of tetralin). The ethers form the following reac