## Abstract The assignment of the carbons of different isomers of methylcyclopentadiene monomers (Me‐CPD) and dimers (diMe‐DCPD) has been performed directly in a mixture, without previous separation of these products, by analysing data from quantitative ^13^C NMR spectra of the mixtures and applyin
Investigation of monomer—dimer equilibria of perfluorocarboxylic acids by second derivative infrared spectroscopy
✍ Scribed by Jeffrey N-P Sun; Peter R. Griffiths; Carleton A. Sperati
- Publisher
- Elsevier Science
- Year
- 1983
- Tongue
- English
- Weight
- 340 KB
- Volume
- 39
- Category
- Article
- ISSN
- 1386-1425
No coin nor oath required. For personal study only.
✦ Synopsis
The equihbrium between monomericand associated forms of pertIuorocarboxylic acids in carbon tetrachloride solution has been studied by Fourier transform infrared spectrometry. It was found that the overlap of the carbonyl stretching bands of the monomer and associated forms was too great to permit the nature of the associated form to be determined accurately. After conversion of the solvent-compensated absorbance spectra to their second derivative and measurement of the height of the secondary maxima of the overlapping bands, the associated species was confirmed to be the dimer.
📜 SIMILAR VOLUMES
H and I3C NMR data for a synthetic dimeric Lewis X octasaccharide derivative { Gal(/?l-4) [ Fuc(u1-3) 1 GlcNAc(/?l-3)Gal(/?1-4) [ Fuc(a1-3)j GlcNAc(/?1-3)Gal(/31-4)Glc [ /?1-(CH,),CO,C,H, 1 } are reported. Some observations on C,H correlations over two and three bonds, which should prove useful in t