The pK, values of the succinic acid moieties of hydrolyzed alternating ethene-and isobutenemaleic anhydride copolymers were determined in D,O. The pD-dependence on the 13C chemical shift of selected signals was analyzed for these copolymers. Four different pK,s were determined for the copolymer with
Structure of alternating cis- and trans-piperylene-maleic anhydride copolymers by 13C-NMR analysis
β Scribed by N.G. Gaylord; M. Nagler; A.C. Watterson
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 176 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0014-3057
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β¦ Synopsis
The copolymerization of the c/s-and trans-piperylene isomers with maleic anhydride in the presence of a peroxide catalyst yields identical equimolar, alternating copolymers which, according to ~C-NMR analyses of the copolymers and the cyclic Diels-Alder adduct from trans-piperylene and maleic anhydride, have trans-methyl group conformation and trans-l,4 unsaturation.
π SIMILAR VOLUMES
The 'H and I3C NMR spectra of an alternating isobutene/maleic anhydride copolymer and the corresponding acid and sodium salt forms were reexamined by 1D and 2D NMR methods. This copolymer contains only threo-succinyl units. The tacticity is characterized by a 53/41 ratio of threo-diisotactic and thr
## Abstract The ^1^H and ^13^C NMR spectra of an alternating ethene/maleic anhydride copolymer and the corresponding acid and sodium salt were reinvestigated with regard to the signals depending on the configuration of the succinyl unit. From these assignments a 85/15 ratio of __threo__βand __eryth
The monomer unit triad sequence distribution and the cidtrans linkage configurations at the cyclic maleic anhydride (MA) units in the copolymers of styrene (ST) and MA prepared in CCI, with AIBN at 50Β°C were quantitatively determined by 13C DEPT NMR spectroscopy. So much as 61 % of the linkages at t
The 'H and "C NMR chemical shift assignments of trans-and cis-10-chlorodecal-2-ones were based on 2D COSY and HETCOR experiments. The spectra were measured either in CDCI, or in C,D, to optimize the spectral dispersion (ASIS effect). Selective spin decoupling experiments were also performed.
The 1 H and 13 C NMR chemical shift assignments of 10-substituted decal-2-ones, cis (H, CH 3 and CO 2 CH 3 ) and trans (H, CH 3 , OH and CO 2 C 2 H 5 ) were based on 2D COSY and HETCOR experiments, supported by selective spin decoupling experiments. The discrimination between the cis and the trans c