1988
DOI: 10.1002/marc.1988.030091001
|View full text |Cite
|
Sign up to set email alerts
|

Macro azo initiators via cationic polymerization. Synthesis and application

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
11
0

Year Published

1992
1992
2013
2013

Publication Types

Select...
4
3
1

Relationship

0
8

Authors

Journals

citations
Cited by 30 publications
(11 citation statements)
references
References 13 publications
0
11
0
Order By: Relevance
“…An entirely different concept towards block copolymer synthesis with a wide range of structure and architecture makes the use of active-center transformation approach. Similarly associating radical-to-cationic polymerization, [214,215] cationic to-radical polymerization [216][217][218] anionic-to-radical polymeri zation , [219] cationic-to-anionic polymerization, [220] anionic-to-cationic polymerization [221] have also been employed successfully to synthesize many novel A-B and ABA-type block copolymers. This transformation involving anions, cations, and radicals is possible.…”
Section: Sequential Polymerizationmentioning
confidence: 99%
“…An entirely different concept towards block copolymer synthesis with a wide range of structure and architecture makes the use of active-center transformation approach. Similarly associating radical-to-cationic polymerization, [214,215] cationic to-radical polymerization [216][217][218] anionic-to-radical polymeri zation , [219] cationic-to-anionic polymerization, [220] anionic-to-cationic polymerization [221] have also been employed successfully to synthesize many novel A-B and ABA-type block copolymers. This transformation involving anions, cations, and radicals is possible.…”
Section: Sequential Polymerizationmentioning
confidence: 99%
“…The greatest progress in living vinyl ether polymerization was made by introducing α-iodo ethers in combination with weak Lewis acids (e.g. ZnI 2 ), iodine, and other moderate acceptors and of α-halogeno ethers in combination with tetraalkylammonium perchlorate as initiator. In 1995, Baird and Wang were the first to report on a metallocene initiator, (η 5 -C 5 Me 5 )TiMe 2 (μ-Me)B(C 6 F 5 ) 3 , for electron rich olefins like vinyl ethers and isobutene .…”
Section: Introductionmentioning
confidence: 99%
“…The other method (eq 2) utilizes the quenching of the HI/ZnI2-initiated living poly(p-alkoxystyrene) with a reagent (7) having a functional group (Z) to be attached to the polymer "tail" ( -end) (end-capping method).46…”
Section: Introductionmentioning
confidence: 99%