Spectroscopic study of 1-decene oligomers obtained with AlCl3 as catalyst
✍ Scribed by Danica Doskočilová; Jan Pecka; Jiří Dybal; Jaroslav Kříž; František Mikeš
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 547 KB
- Volume
- 195
- Category
- Article
- ISSN
- 1022-1352
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The product of 1‐decene oligomerization with AlCl~3~ as catalyst was fractionated by vacuum distillation, with the highest fraction consisting predominantly of the hexamer. The structure of the fractions was characterized by ^1^H and ^13^C NMR and Raman spectroscopy. The oligomers contain predominantly long branches (7 carbons and longer) and always one double bond per molecule, with strong predominance of tri‐ and tetra‐substituted types. The minority structures are analyzed, and the polymerization and isomerization mechanisms are discussed.
📜 SIMILAR VOLUMES
The cationic transannular polymerization of cis,cis-l,5-cyclooctadiene (COD) initiated by Ziegler-Natta catalysts of the type Cp2MCI: (M = Ti, Zr, HI) with various alkylaluminium compounds, such as Et3A1, Et2AIC1 and Et3A12CI 3, was studied. The order of activity of these catalysts depends on the me
Product distribution and kinetic studies on the hydrosilylation of phenylacetylene by Ph 3 SiH, Ph 2 MeSiH, PhMe 2 SiH and Et 3 SiH were performed using bis-[1,2-diphenylphosphinoethane]norbornadienerhodium(I) hexafluorophosphate, 1, as catalyst. Pre-equilibration of the catalyst with the acetylene