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Dilute solution properties of polybutadiene modified by 4-phenyl-1,2,4-triazoline-3,5-dione

โœ Scribed by Clara I. D. Bica; Walther Burchard; Reimund Stadler


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
859 KB
Volume
197
Category
Article
ISSN
1022-1352

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โœฆ Synopsis


Abstract

The dilute solution properties of 4โ€phenylโ€1,2,4โ€triazolineโ€3,5โ€dioneโ€modified polybutadienes were studied in tetrahydrofuran by static and dynamic light scattering and compared with those from unmodified polybutadiene chains. For the unmodified polymer, the scaling laws were established and the coil interpenetration parameter k was determined in the thermodynamically good solvent tetrahydrofuran; the chains exhibited common flexible chain behavior. For the modified polybutadiene, the results indicate at infinite dilution a weak extent of intermolecular crosslinking via the urazole groups, coupled with a very high extent of intramolecular ring formation. In order to evaluate the fraction of rings, an analysis of the association equilibrium by Fourierโ€transform infrared spectroscopy (FTIR) was performed in the absorption region of the carbonyl stretching vibration of the urazole ring.


๐Ÿ“œ SIMILAR VOLUMES


Solvent Effects in [4+2] Cycloadditions
โœ Sauer, Jรผrgen ;Schuhbauer, Hans Markus ๐Ÿ“‚ Article ๐Ÿ“… 1997 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 497 KB

## Abstract Relative rates of [4 + 2] cycloadditions of cyclopentadienes 1aโ€“1e with 4โ€phenylโ€1,2,4โ€triazolineโ€3,5โ€dione (2) in 12 different solvents vary by factors of up to 19000, but the reactions show similar solvent effects. Rate constants __k__~2~ correlate well with solvent parameters __AN__