Nitrones are arguably one of the most efficient compounds with multi-functional capabilities, acting as both radical spin traps and 1,3-dipoles. In contrast to their potential synthetic versatility, the application of nitrones in synthetic polymer chemistry is still in its infancy and its true potential has yet to be fully explored. The current report thus serves as a highlight and provides an update on the current status of nitrones in macromolecular synthesis. © The Royal Society of Chemistry 2011
International audienceA novel series of α-phenyl-N-tert-butyl nitrone derivatives, bearing a hydroph...
The identification and quantification of spin adducts and their reduction products (>NOH, >NOR) form...
The current review focuses on the relevance and practical benefit of interpolymer radical coupling m...
Nitrones are arguably one of the most efficient compounds with multi-functional capabilities, acting...
A series of cyclic nitrones have been tested for their spin-trapping activity in the enhanced spin-c...
A series of cyclic nitrones have been tested for their spin-trapping activity in the enhanced spin-c...
Two novel macromolecular engineering protocols termed enhanced spincapturing polymerization (ESCP) a...
A synthetic strategy employing nitrones as radical spin traps is presented on the example of the eff...
A series of cyclic nitrones have been tested for their spin-trapping activity in the enhanced spin-c...
Nitrones are demonstrated to efficiently mediate radical coupling reactions on the example of the co...
A novel nitrone (α-4-(3-(trimetliylsilyl)prop-2-ynyloxy)-N-tert-butyl nitrone) with an alkyne "click...
The ability of several nitrones to control the radical polymerization of styrene at 110 °C has been ...
Macromolecules containing Nitrone moieties were prepared by oxidation of imines formed by the reacti...
The ability of several nitrones to control the radical polymerization of styrene at 110 °C has been ...
A facile method to generate polymer materials with embedded functional groups at known and precise p...
International audienceA novel series of α-phenyl-N-tert-butyl nitrone derivatives, bearing a hydroph...
The identification and quantification of spin adducts and their reduction products (>NOH, >NOR) form...
The current review focuses on the relevance and practical benefit of interpolymer radical coupling m...
Nitrones are arguably one of the most efficient compounds with multi-functional capabilities, acting...
A series of cyclic nitrones have been tested for their spin-trapping activity in the enhanced spin-c...
A series of cyclic nitrones have been tested for their spin-trapping activity in the enhanced spin-c...
Two novel macromolecular engineering protocols termed enhanced spincapturing polymerization (ESCP) a...
A synthetic strategy employing nitrones as radical spin traps is presented on the example of the eff...
A series of cyclic nitrones have been tested for their spin-trapping activity in the enhanced spin-c...
Nitrones are demonstrated to efficiently mediate radical coupling reactions on the example of the co...
A novel nitrone (α-4-(3-(trimetliylsilyl)prop-2-ynyloxy)-N-tert-butyl nitrone) with an alkyne "click...
The ability of several nitrones to control the radical polymerization of styrene at 110 °C has been ...
Macromolecules containing Nitrone moieties were prepared by oxidation of imines formed by the reacti...
The ability of several nitrones to control the radical polymerization of styrene at 110 °C has been ...
A facile method to generate polymer materials with embedded functional groups at known and precise p...
International audienceA novel series of α-phenyl-N-tert-butyl nitrone derivatives, bearing a hydroph...
The identification and quantification of spin adducts and their reduction products (>NOH, >NOR) form...
The current review focuses on the relevance and practical benefit of interpolymer radical coupling m...