Sterically hindered a-glycols, obtained from electrochemical hydrodimenhation of polycyclic ketones (idanone, tetralone, chromanone, flavanone, xanthone and fluorenone), were studied by 'H and -C NMR. Evidence of conformational hindrance was deduced from the 'H spectra; meso or racemic configuration
Preparation and 13C NMR spectroscopy of uniform oligopropylene glycols
โ Scribed by C. Campbell; F. Heatley; G. Holcroft; C. Booth
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 491 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0014-3057
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โฆ Synopsis
Samples of di-, tetra-and octapropylene glycols which are uniform in chain length have been prepared and studied by ~3C NMR spectroscopy, with CH and CH 2 subspectra obtained by the DEPT technique. A pure sample of the head-to-head isomer of dipropylene glycol was prepared, but other samples were mixtures of regioisomers. All the resonances of the head-to-tail and the head-to-head isomers of dipropylene glycol were assigned, as well as a number of resonances of the higher oligomers, including those due to carbons adjacent to hydroxyl end groups. Overall structural parameters were determined, i.e. the fraction of secondary hydroxyl ends, the fraction of interior CH groups in head-to-head placements, and the fraction of CH 2 groups in tail-to-tail placements. A reactivity ratio for condensation of secondary vs primary end groups was also determined.
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Several procedures for synthesis of stereoregular poly(methacrylic acid) have been examined and the polymer characterized by (I~C)NMR. Using d 6 DMSO as solvent for spectroscopy gives better spectra than those previously obtained using aqueous solutions and stereoehemical splittings can be resolved
Be 1 g i u m biaceae), and of six common acyl substituents of naturally occurring phorbol esters were recorded and the signals assigned. The spectral data for this series of model compounds appeared to be important tools for the identification and the structure elucidation of naturally occurring and