G
Ghislain David
Researcher at Centre national de la recherche scientifique
Publications - 124
Citations - 3638
Ghislain David is an academic researcher from Centre national de la recherche scientifique. The author has contributed to research in topics: Radical polymerization & Monomer. The author has an hindex of 28, co-authored 120 publications receiving 2891 citations. Previous affiliations of Ghislain David include Commissariat à l'énergie atomique et aux énergies alternatives & École Normale Supérieure.
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Journal ArticleDOI
RAFT polymerization of dimethyl(methacryloyloxy)methyl phosphonate and its phosphonic acid derivative: a new opportunity for phosphorus-based materials
TL;DR: In this article, the RAFT polymerization of dimethyl(methacryloyloxy)methyl phosphonate (MAPC1) using dithioester chain transfer agents is reported for the first time to our knowledge in the literature.
Book ChapterDOI
Telechelic Oligomers and Macromonomers by Radical Techniques
TL;DR: In this paper, a review summarizes nearly 400 references (since 1990) intended to highlight directions on the synthesis of telechelic oligomers and macromonomers by radical techniques, taking into account the recent developments in conventional radical polymerizations, such as dead-end polymerizationand also telomerization reactions.
Journal ArticleDOI
New method for the synthesis of formaldehyde-free phenolic resins from lignin-based aldehyde precursors
TL;DR: In this paper, a method to functionalize phenolic compounds with aliphatic aldehydes by a two-step reaction was proposed, i.e., the functionalization of an acetal group on aromatic hydroxyl functions and the subsequent deprotection of theses acetal groups into aldehyde groups.
Journal ArticleDOI
Aromatic dialdehyde precursors from lignin derivatives for the synthesis of formaldehyde-free and high char yield phenolic resins
TL;DR: In this article, reactivity of aromatic aldehydes has been studied in function of the nature and positions of aromatic substituents prior to the aldehyde function, and it was shown that those bio-based compounds are not reactive in resol synthesis reactions but their reactivity can be triggered by masking their free-hydroxy groups.
Journal ArticleDOI
Vanillin-derived amines for bio-based thermosets
TL;DR: In this paper, new bio-based amine monomers derived from vanillin were prepared by the direct amination of an epoxy monomer with aqueous ammonia, and these synthesized amines exhibited high reactivity due to the presence of secondary OH groups.