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Heterocycles polymerization

Generally, the vinyl heterocycles polymerize under the influence of a radical initiator, but, under such conditions, thiols react with 1-vinylpyrroles to give the expected addition products (77KGS1636). [Pg.282]

The reduced probability of side reactions enables some heterocycle polymerizations to proceed by a living mechanism. [Pg.194]

The organization of the book follows a logical sequence After a thorough presentation of basic thermodynamic principles and the Jacobson-Stockmayer cycliza-tion theory, the authors discuss in depth all kinds of aspects of the various heterocyclic compound classes. In addition to detailed discussions of mechanisms, many other facets of heterocyclic polymerizations are treated, e.g., monomer synthesis, contemporary research trends, industrial significance. The treatise ends with an excellent up-to-date discussion of random, block and graft copolymerizations of heterocyclics. [Pg.327]

In contrast to the heterocyclic polymerizations, (TPP)AICI does not initiate polymerization of methacrylates [76] and me-thacrylonitrile [77], whereas (TPP)AlMe initiation requires irradiation by visible light. These extremely slow polymerizations are also accelerated by addition of... [Pg.134]

Anionic and Cationic Polymerizations o Radical Polymerization Advances o Coordination Polymerizations 0 Step-Growth Polymerization Advances 0 Synthesis of Tactic Polymers o Stereoblock Copolymers o Dispersion Polymerizations o Cellulosic Graft Copolymers o Diels-Alder Polymer Forming Reactions o A New Path To Phenolic Resins o Nitrogen Heterocycle Polymerizations o Optically Active Polymers o Poly (Phenylene Sulfide) o Poly (Aryl Ethers) o (Poly (Aryl Ether Sulfones) o Epoxy and Isocyanate Resin Replacement o Azlactone Functionalized Oligomers o Epoxy Resin-Isocyanate Reactions o Chelating Polymers o Oxazoline Functionalized Polymers o Poly (Alkyl Methacrylates) o Macromers... [Pg.559]

Boron Nitride. B-N-C Heterocycles. Polymeric B-N Compounds. Literature coverage from 1950 up to 1972. [Pg.273]

Certain heterocycles polymerize by very peculiar reaction pathways. For example, the cationic polymerization of lactams proceeds by activation of the monomer, as for their anionic polymerization ... [Pg.336]


See other pages where Heterocycles polymerization is mentioned: [Pg.261]    [Pg.259]    [Pg.3]    [Pg.28]    [Pg.50]    [Pg.183]    [Pg.185]    [Pg.187]    [Pg.189]    [Pg.191]    [Pg.193]    [Pg.15]    [Pg.327]    [Pg.11]    [Pg.248]    [Pg.26]   
See also in sourсe #XX -- [ Pg.346 , Pg.362 ]




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Cationic heterocyclic polymerization

Cationic heterocyclic polymerization Initiation mechanism

Chain polymerization heterocyclic monomers

Heterocyclic monomers, ring-opening polymerization

Other Cationic Polymerizations Heterocyclic Monomers

Polymerization of Heterocyclics

Ring-opening polymerization of heterocyclic monomers

Ring-opening polymerization sulfur heterocyclics

Sulfur heterocyclic polymerization

Transfers during polymerization of heterocyclic monomers

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