## Abstract **Summary:** The configurational sensitivity of the chemical shift of methylene carbons has been analyzed theoretically in terms of a perturbative approach. Theoretical results and computations have been applied successfully to new experimental data obtained from model compounds of the
Simple Trends in NMR Spectra of Vinyl Polymers: The 1H NMR Spectrum of Poly(propylene)
β Scribed by Guglielmo Monaco; Adolfo Zambelli
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 118 KB
- Volume
- 206
- Category
- Article
- ISSN
- 1022-1352
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β¦ Synopsis
Abstract
Summary: The tacticity spreading of chemical shifts in the proton NMR spectrum of poly(propylene) in solution has been analyzed first qualitatively, taking advantage of known trends in both proton chemical shift and conformational statistics of vinyl polymers as summarized in the telephone rule, and then quantitatively using ab initio computations, empirical additivity schemes of proton chemical shifts, and conformational averages according to models of different rotational isomeric states. The very good results obtained, both qualitatively and quantitatively, stem from the relatively easy parametrization of proton chemical shift and establish a successful application of the telephone rule, also for proton NMR spectra.
Anti and syn labeling of methylene hydrogens in m and r diads.
magnified image__Anti__ and syn labeling of methylene hydrogens in m and r diads.
π SIMILAR VOLUMES
## Abstract **Summary:** Chemical shift trends in the methylene and __Ξ±__ substituent regions of ^13^C NMR spectra of vinyl polymers have been analyzed in terms of a threeβstate rotational isomeric states (RIS) model and the __Ξ³__β__gauche__ effect. In this framework, it has been demonstrated that
## Abstract The ^13^C NMR spectrum of anisomycin and the ^1^H and ^13^C NMR spectra of deacetylanisomycin were assigned using oneβ and twoβdimensional NMR analysis. The techniques included INEPT, ^1^Hο£Ώ^13^C HETCORR and ^1^Hβ^1^H COSY spectroscopy.
## Abstract Reassignment of the ^1^H and ^13^C NMR spectra of fusidic acid and the total assignment of lumifusidic acid and some important diβ and tetraβhydrofusidic acid derivatives are reported. Copyright Β© 2002 John Wiley & Sons, Ltd.