The cationic polymerization of octadecyl vinyl ether (ODVE) initiated by trimethylsilyl iodide and 1,l-diethoxyethane in the presence of ZnI, in toluene at 0°C and 10°C has been investigated. For molecular weights lower than 6000, a linearity of M,, with conversion was observed, but for higher molec
Synthesis of Soluble Poly(Divinylbenzene) with an End-Functional Group
✍ Scribed by Yukio Nagasaki; Masao Kato; Norikiyo Kato; Yoshio Mitsuhata; Hiroaki Nishizuka; Teiji Tsuruta
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2010
- Weight
- 435 KB
- Volume
- 99
- Category
- Article
- ISSN
- 0037-9646
No coin nor oath required. For personal study only.
✦ Synopsis
Synthetic methods of end-functional soluble poly(diviny1benzene) [poly DVB)] and A-B-A pe block copolymers having soluble poly(diviny1benzene) segments were investigatedl Lithium N, N'-bi$rimethylsil 1)ethylenediamine was found to initiate an anionic polymerization of 1 ,4-dbinylbenzene (DVB) to form soyuble polymer havin one N,N'-bis trimethy1silyl)ethylenediamine moiety at the end of 01 rner chain almost quantitatively. The potmer was eash y converted to primary-amino-ended soluble pol@dlJ by treating with tetrabutylammonium fluoride. Lithiated trimethylallylsilane also had an initiation ability or DV polymerization. Ween the pol merization was carried out by lithiated trimethylallylsilane, in the presence of diisopropylamine, a soluble pormer was formed. The polymer obtained had one terminal organosilyl group and reactive pendent vinyrgroup in each monomeric unit. A-B-A T e tri block copolymer was synthesized through reactions between primary-amino-ended soluble p o l y ( D 4 anda,o-bis-primary-amino-ended silicone using 4,4'-diphenylmethanediisocyanate as coupling agent. The resulting polymer was a multi-functional polymer having poly(DVB) segments and silicone segments.
📜 SIMILAR VOLUMES
The bulk polymerization of tetrahydrofuran (THF) intiated by methyl triflate or triflic anhydride leads to poly-THF's of polydispersity < 1.2 and possessing one or two oxonium chain ends, if the conversion is kept below 15}~. Reaction of these "living" polymers with an N-substituted azetidine leads
## Abstract Amorphous poly[(__R__,__S__)‐ß‐hydroxybutyrate], containing both phosphonoacetate and carboxylate functional end groups, was synthesized via anionic polymerization of racemic ß‐butyro‐lactone initiated by supramolecular complexes of potassium __P__,__P__‐dimethylphosphonoacetate. The li
## Abstract Telechelic polystyrenes with five benzyl chloride moieties at the polymer end (PSt‐E) were prepared by coupling reaction of polystyryllithium with hexakis(4‐chloromethyl‐phenoxy)cyclotriphosphazene (4). The coupling reaction occurs almost quantitatively and unfavorable side reactions we