The preferred conformations and, for the 3-methyl-substituted analogues also the configurations of the C-3 atom, for 3-unsubstituted and 3-methyl-substituted di-exo-and di-endo-annellated oxazepinone derivatives fused with a norbornane or norbornene skeleton were determined by 'H and 13C NMR spectro
Configurational-conformational entropy of 1,4-polydienes
✍ Scribed by Zhou, Zhiping ;Yan, Deyue ;Alfonso, Giovanni Carlo
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1993
- Weight
- 427 KB
- Volume
- 2
- Category
- Article
- ISSN
- 1018-5054
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
A method based on matrix algebra and on the rotational isomeric state scheme to study the configurational‐ conformational entropy of 1,4‐polydienes with geometrical isomerism has been developed. Bernoullian and first‐and second‐order Markovian statistics for the sequences of cis and trans units along the chains have been considered, and the explicit relation between entropy and mole fraction of cis units has been derived. Calculations performed by using available experimental data for the configurational parameters and the conformational partition functions of 1,4‐polybutadiene and 1,4‐polyisoprene show that entropy is a monotonic function of the geometrical isomer composition. While the entropy of polybutadiene increases with the content of cis units, the reverse is true for polyisoprene.
📜 SIMILAR VOLUMES
Oriented specimens of isotactic cis-l,4-poly(3-methyl-l,3-pentadiene) exhibit two crystalline modifications characterized, respectively, by the expected two-fobd helical conformation with a fiber repeat of 8,02 A and by a three-fold helix with c = 9,97 A. The latter highly contracted structure is pr
## Abstract The dependence of the configurational‐conformational characteristics, such as the mean‐square end‐to‐end distance, the mean‐square radius of gyration, and the temperature coefficient of the stereoirregular polystyrene chains on the fraction of __meso__ dyads, __P__~__m__~ was investigat
The configuration and conformation of some diastereomeric 4-hydroxy-cis-and -h.uns-l-oxadecalins were inferred by 'H and '3C NMR spectroscopy. The results obtained indicate that the cis-fused compounds are conformationally homogeneous, having the oxygen atom attached to the cyclohexyl ring in the ax
Poly(itaconic acid) esters with oligo(ethylene oxide) side chains can form amorphous solid solutions with LiClO 4 and NaClO 4 . Many research groups have examined AC ionic conductivities of these polymer/salt mixtures as a function of side-chain length and salt concentration. We propose a model to i