A click chemistry synthetic strategy based on aza-Michael addition and radical photopolymerization is proposed to generate a polymeric network via three time-controlled steps. The selection of primary diamines and diacrylates allows two consecutive aza-Michael reactions to occur. This reaction sequence affords the unique opportunity to interpose a radical photopolymerization reaction, enhancing the cross-link density. Consequently, the second aza-Michael addition appears as a valuable postconsolidation step of the polymer network
Polymeric networks have been intensely investigated and a large number of applications have been fou...
The ability to combine two polymerization mechanisms in a one-pot setup and switch the monomer selec...
Radical-mediated thiol−yne step-growth photopolymerizations are utilized to form highly cross-linked...
atom transfer radical polymerization (ATRP); azide-alkyne cycloaddition; click chemistry; controlled...
In the present thesis, well-defined complex polymeric architectures are realized via a combination o...
ABSTRACT: Photochemical processes enable spatial and temporal control of reactions, which can be imp...
Although the aza-Michael addition reaction on various unsaturated (di-)carboxylic acids and esters o...
Le concept de "Chimie Click" a été introduit par Sharpless en 2001 [1] pour décrire une série de réa...
Controlled radical polymerization methods and click chemistry form a versatile toolbox for creating ...
© 2016 Dr. Thomas George McKenzieThe synthesis of polymers with controlled molecular weights, design...
This paper highlights the powerful combination of reversible addition–fragmentation chain transfer (...
Click reaction is a very fast, high yield with no byproduct, biocompatible, tolerant to surrounded m...
Azidopropyl methacrylate (AzPMA), a functional monomer with a pendent azido group, polymerizes from ...
Polymeric networks have been intensely investigated and a large number of applications have been fou...
Conceptually new one-pot photoinduced sequential click reactions were implemented to yield novel blo...
Polymeric networks have been intensely investigated and a large number of applications have been fou...
The ability to combine two polymerization mechanisms in a one-pot setup and switch the monomer selec...
Radical-mediated thiol−yne step-growth photopolymerizations are utilized to form highly cross-linked...
atom transfer radical polymerization (ATRP); azide-alkyne cycloaddition; click chemistry; controlled...
In the present thesis, well-defined complex polymeric architectures are realized via a combination o...
ABSTRACT: Photochemical processes enable spatial and temporal control of reactions, which can be imp...
Although the aza-Michael addition reaction on various unsaturated (di-)carboxylic acids and esters o...
Le concept de "Chimie Click" a été introduit par Sharpless en 2001 [1] pour décrire une série de réa...
Controlled radical polymerization methods and click chemistry form a versatile toolbox for creating ...
© 2016 Dr. Thomas George McKenzieThe synthesis of polymers with controlled molecular weights, design...
This paper highlights the powerful combination of reversible addition–fragmentation chain transfer (...
Click reaction is a very fast, high yield with no byproduct, biocompatible, tolerant to surrounded m...
Azidopropyl methacrylate (AzPMA), a functional monomer with a pendent azido group, polymerizes from ...
Polymeric networks have been intensely investigated and a large number of applications have been fou...
Conceptually new one-pot photoinduced sequential click reactions were implemented to yield novel blo...
Polymeric networks have been intensely investigated and a large number of applications have been fou...
The ability to combine two polymerization mechanisms in a one-pot setup and switch the monomer selec...
Radical-mediated thiol−yne step-growth photopolymerizations are utilized to form highly cross-linked...