Proton magnetic resonance of some polyalkenamers and some ethylene-propylene copolymers
โ Scribed by A. Chierico; G. Del Nero; G. Lanzi; E.R. Mognaschi
- Publisher
- Elsevier Science
- Year
- 1969
- Tongue
- English
- Weight
- 477 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0014-3057
No coin nor oath required. For personal study only.
โฆ Synopsis
This paper is devoted to a comparative study, performed by means of NMR, of properties and behaviour of an homologous series of polyalkenamers and of some ethylene-propylene copolymers. It was observed that, in polyalkenamers, the chain mobility depends on the number of methylene groups present between two subsequent double bonds. An analogous dependence was observed, in the copolymers studied, on the ethylene-propylene ratio. It is pointed out that it is more suitable, in the study of polymers, to examine a series of comparable samples than to study separately a single polymer.
๐ SIMILAR VOLUMES
## Abstract The chemical shifts and coupling constants for the ring protons of nine disubstituted naphthalenes (mainly halogenonitre compounds) in carbon tetrachloride solutions have been obtained by analysis and computer simulation of their 100 MHz magnetic resonance spectra. Substituent effects a
## Abstract An accurate measurement of the chemical shifts and the coupling constants of some disubstituted acetophenones has been made. The acetophenones studied contained nitro, bromo or amino groups substituted in either the 3,4 or 2,5 positions. For compounds with no substituent adjacent to the
Proton and boron-1 1 magnetic resonance spectra for several potassium para-substituted tetraarylborate compounds [KB(C6Ha-pX)4, where X is H, OCH,, CHa, Br, C1, F, CF,] have been obtained. The chemical shift between the centers of the AA' and XX' multiplets for the ring proton multiplets, relative t