𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Microstructure of polymers obtained by cationic polymerization of endo-dicyclopentadiene

✍ Scribed by Yu Xing Peng; Jia Lin Liu; Lin Feng Cun


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
274 KB
Volume
34
Category
Article
ISSN
0887-624X

No coin nor oath required. For personal study only.

✦ Synopsis


SYNOPSIS

endo-Dicyclopentadiene (DCPD) was polymerized by various cationic initiating systems in different solvents. IR and 'H NMR results show that four types of structural units are formed due to the corresponding addition modes: the addition on the norhornenic (NB) double bond generates unit I and rearranged unit 11, while the addition on the cyclopentenic (CP) double bond produces unit I11 and rearranged unit IV. The reaction medium has a stronger effect on the microstructure of the polymer (PDCPD) than initiating systems. The polymers prepared in toluene and n-hexane contain all four structural units, while the polymer produced in methylene chloride is composed of structural units I1 and IV.


πŸ“œ SIMILAR VOLUMES


Preparation of cationic polymer surfaces
✍ H. Yasuda; B. Sherry; M. A. Ei-Nokaly; S. E. Friberg πŸ“‚ Article πŸ“… 1982 πŸ› John Wiley and Sons 🌐 English βš– 480 KB πŸ‘ 1 views

A cationic polymer surface with extensive capacity for adsorption of anionic surfactants was prepared by graft polymerization of vinyl pyridine onto a plasma-treated polypropylene surface. The nitrogen was quaternized in order to obtain the cationic sites. The concentration dependence of adsorption

Functional polysiloxanes. I. Microstruct
✍ Patrick CancouΓ«t; Elodie Daudet; GΓ©rard HΓ©lary; Michel Moreau; Georges Sauvet πŸ“‚ Article πŸ“… 2000 πŸ› John Wiley and Sons 🌐 English βš– 231 KB

Poly(hydrogenmethylsiloxane-co-dimethylsiloxane)s of various compositions have been prepared by cationic ring-opening polymerization of octamethylcyclotetrasiloxane (D 4 ) and 1,3,5,7-tetramethylcyclotetrasiloxane (D 4 H ) in the presence of hexamethyldisiloxane as end-blocker or by rearrangement of