Controlled synthesis of branched poly(vinyl acetate)s by xanthate-mediated RAFT self-condensing vinyl (co)polymerization

2011 ◽  
Vol 2 (10) ◽  
pp. 2231 ◽  
Author(s):  
Julien Schmitt ◽  
Nicolas Blanchard ◽  
Julien Poly
Keyword(s):  
Vinyl Acetate ◽  
Controlled Synthesis

Controlled Synthesis of Fluorinated Copolymers via Cobalt-Mediated Radical Copolymerization of Perfluorohexylethylene and Vinyl Acetate

2017 ◽  
Vol 50 (10) ◽  
pp. 3750-3760 ◽  
Author(s):  
Jérémy Demarteau ◽  
Bruno Améduri ◽  
Vincent Ladmiral ◽  
Maarten A. Mees ◽  
Richard Hoogenboom ◽  
...  
Keyword(s):  
Vinyl Acetate ◽  
Radical Copolymerization ◽  
Controlled Synthesis ◽  
Fluorinated Copolymers

Controlled synthesis of poly(vinyl acetate) by traditional radical emulsion polymerization

2016 ◽  
Vol 65 (12) ◽  
pp. 1382-1386 ◽  
Author(s):  
Yu Guan ◽  
Jingjing Li ◽  
Leishan Shao ◽  
Fei Wang ◽  
Dongyu Dong ◽  
...  
Keyword(s):  
Emulsion Polymerization ◽  
Vinyl Acetate ◽  
Controlled Synthesis

Inhibition of Radical-Initiated Vinyl Acetate Polymerisation by Tobacco Smoke Fractions

1974 ◽  
Vol 7 (5) ◽  
Author(s):  
M.A. Nisbet ◽  
S. Schmeller
Keyword(s):  
Benzoyl Peroxide ◽  
Vinyl Acetate ◽  
Tobacco Smoke ◽  
Boiling Point ◽  
Water Bath ◽  
Measuring Time ◽  
Time Required

AbstractBoth the vapour and particulate phases of tobacco smoke have been shown to retard benzoyI-peroxide-initiated polymerisation of vinyl acetate by interception of the radicals involved in the polymerisation process. The extent of inhibition of polymerisation by test compounds is estimated by measuring time taken for a mixture of monomer and benzoyl peroxide, immersed in a water-bath at 70°C, to reach a spontaneous boil and comparing it with the time required for a similar mixture with added retarder to reach boiling point. Units are expressed as minutes of inhibition per part per million of inhibitor × 10

Seeded Growth of Single-Crystal Two-Dimensional Covalent Organic Frameworks

2017 ◽  
Author(s):  
Austin M. Evans ◽  
Lucas R. Parent ◽  
Nathan C. Flanders ◽  
Ryan P. Bisbey ◽  
Edon Vitaku ◽  
...  
Keyword(s):  
Molecular Transport ◽  
Controlled Synthesis ◽  
Two Dimensional ◽  
Covalent Organic Frameworks ◽  
Seeded Growth ◽  
Covalent Bonds ◽  
Crystalline Materials ◽  
Step Procedure ◽  
Structures And Properties ◽  
2D Polymer

<div> <div> <div> <p>Polymerizing monomers into periodic two-dimensional (2D) networks provides structurally precise, atomically thin macromolecular sheets linked by robust, covalent bonds. These materials exhibit desirable mechanical, optoelectrotronic, and molecular transport properties derived from their designed structure and permanent porosity. 2D covalent organic frameworks (COFs) offer broad monomer scope, but are generally isolated as polycrystalline, insoluble powders with limited processability. Here we overcome this limitation by controlling 2D COF formation using a two- step procedure. In the first step, 2D COF nanoparticle seeds are prepared with approximate diameters of 30 nm. Next, monomers are slowly added to suppress new nucleation while promoting epitaxial growth on the existing seeds to sizes of several microns. The resulting COF nanoparticles are of exceptional and unprecedented quality, isolated as single crystalline materials with micron-scale domain sizes. These findings advance the controlled synthesis of 2D layered COFs and will enable a broad exploration of synthetic 2D polymer structures and properties. </p> </div> </div> </div>

Seeded Growth of Single-Crystal Two-Dimensional Covalent Organic Frameworks

2017 ◽  
Author(s):  
Austin M. Evans ◽  
Lucas R. Parent ◽  
Nathan C. Flanders ◽  
Ryan P. Bisbey ◽  
Edon Vitaku ◽  
...  
Keyword(s):  
Molecular Transport ◽  
Controlled Synthesis ◽  
Two Dimensional ◽  
Covalent Organic Frameworks ◽  
Seeded Growth ◽  
Covalent Bonds ◽  
Crystalline Materials ◽  
Step Procedure ◽  
Structures And Properties ◽  
2D Polymer

<div> <div> <div> <p>Polymerizing monomers into periodic two-dimensional (2D) networks provides structurally precise, atomically thin macromolecular sheets linked by robust, covalent bonds. These materials exhibit desirable mechanical, optoelectrotronic, and molecular transport properties derived from their designed structure and permanent porosity. 2D covalent organic frameworks (COFs) offer broad monomer scope, but are generally isolated as polycrystalline, insoluble powders with limited processability. Here we overcome this limitation by controlling 2D COF formation using a two- step procedure. In the first step, 2D COF nanoparticle seeds are prepared with approximate diameters of 30 nm. Next, monomers are slowly added to suppress new nucleation while promoting epitaxial growth on the existing seeds to sizes of several microns. The resulting COF nanoparticles are of exceptional and unprecedented quality, isolated as single crystalline materials with micron-scale domain sizes. These findings advance the controlled synthesis of 2D layered COFs and will enable a broad exploration of synthetic 2D polymer structures and properties. </p> </div> </div> </div>

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