Daniel Taton

Prof. Daniel Taton

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Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 March 2023 in Chemical Reviews
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Journal Article
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VTVincent Tournier
Vincent Tournier
SDSophie Duquesne
Sophie Duquesne
FGFrédérique Guillamot
Frédérique Guillamot
HCHenri Cramail
Henri Cramail
DTDaniel Taton
Daniel Taton
IAIsabelle André
Isabelle André

4 January 2013 in Chemical Society Reviews
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Journal Article
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MFMaréva Fèvre
Maréva Fèvre
Julien PinaudJulien Pinaud
Julien Pinaud
YGYves Gnanou
Yves Gnanou
JVJoan Vignolle
Joan Vignolle
DTDaniel Taton
Daniel Taton
The chemistry of N-heterocyclic carbenes (NHCs) has witnessed tremendous development in the past two decades: NHCs have not only become versatile ligands for transition metals, but have also emerged as powerful organic catalysts in molecular chemistry and, more recently, in metal-free polymer synthesis. To understand the success of NHCs, this review first presents the electronic properties of NHCs, their main synthetic methods, their handling, and their reactivity. Their ability to activate key functional groups (e.g. aldehydes, esters, heterocycles, silyl ketene acetals, alcohols) is then discussed in the context of molecular chemistry. Focus has been placed on the activation of substrates finding analogies with monomers (e.g. bis-aldehydes, multi-isocyanates, cyclic esters, epoxides, N-carboxyanhydrides, etc.) and/or initiators (e.g. hydroxy- or trimethylsilyl-containing reagents) employed in such “organopolymerisation” reactions utilizing NHCs. A variety of metal-free polymers, including aliphatic polyesters and polyethers, poly(α-peptoid)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way. The last section covers the use of NHCs as structural components of the polymer chain. Indeed, NHC-based photoinitiators, chain transfer agents or functionalizing agents, as well as bifunctional NHC monomer substrates, can also serve for metal-free polymer synthesis.

9 April 2012 in Journal of the American Chemical Society
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Journal Article
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MFMaréva Fèvre
Maréva Fèvre
Julien PinaudJulien Pinaud
Julien Pinaud
ALAlexandre Leteneur
Alexandre Leteneur
YGYves Gnanou
Yves Gnanou
JVJoan Vignolle
Joan Vignolle
JSJean-Marc Sotiropoulos
Jean-Marc Sotiropoulos

16 August 2008 in Macromolecules
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Journal Article
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KVKari Vijayakrishna
Kari Vijayakrishna
SJSuresh K. Jewrajka
Suresh K. Jewrajka
ARAlaitz Ruiz
Alaitz Ruiz
RMRebeca Marcilla
Rebeca Marcilla
Jose A. PomposoJose A. Pomposo
Jose A. Pomposo
YGYves Gnanou
Yves Gnanou

21 May 2010 in Langmuir
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Journal Article
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WAWilly Agut
Willy Agut
ABAnnie Brûlet
Annie Brûlet
CSChristophe Schatz
Christophe Schatz
DTDaniel Taton
Daniel Taton
Sebastien LecommandouxSebastien Lecommandoux
Sebastien Lecommandoux