Ghislain DAVID

Dr. Ghislain DAVID

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Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

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

Representative Publications

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5 August 2015 in RSC Advances
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Journal Article
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RMRaphaël Ménard
Raphaël Ménard
CNClaire Negrell
Claire Negrell
MFMaxence Fache
Maxence Fache
Laurent FERRYLaurent FERRY
Laurent FERRY
Rodolphe SonnierRodolphe Sonnier
Rodolphe Sonnier
GDGhislain DAVID
Ghislain DAVID
In this work, phloroglucinol was used as a renewable resource to prepare an epoxy monomer and phosphorus containing reactive flame retardant (FR).

20 May 2010 in Macromolecules
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Journal Article
Closed access
RTRussell Tayouo
Russell Tayouo
GDGhislain DAVID
Ghislain DAVID
BABruno Améduri
Bruno Améduri
JRJacques Rozière
Jacques Rozière
SRStephanie Roualdes
Stephanie Roualdes

1 August 2018 in Green Chemistry
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Journal Article
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AMAnne-Sophie Mora
Anne-Sophie Mora
RTRussell Tayouo
Russell Tayouo
BBBernard Boutevin
Bernard Boutevin
GDGhislain DAVID
Ghislain DAVID
Sylvain CaillolSylvain Caillol
Sylvain Caillol
In the scope of fully bio-based materials development, access to bio-based aromatic amine monomers is one of the main industrial challenges over the coming years.

18 July 2022 in Carbohydrate Polymers
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Journal Article
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LMLorelei Meyer-Déru
Lorelei Meyer-Déru
GDGhislain DAVID
Ghislain DAVID
RARémi Auvergne
Rémi Auvergne

1 December 2006
Verified
Book Chapter
Closed access
PDF file
BBB. Boutevin
B. Boutevin
GDGhislain DAVID
Ghislain DAVID
CBC. Boyer
C. Boyer

23 September 2011 in Polymer Chemistry
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Journal Article
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GDGhislain DAVID
Ghislain DAVID
CNC. Negrell-Guirao
C. Negrell-Guirao
FIF. Iftene
F. Iftene
BBB. Boutevin
B. Boutevin
KCK. Chougrani
K. Chougrani
This review paper gathers almost one hundred recent publications devoted to the synthesis and the free radical (co)polymerization of phosphonate vinyl monomers. Different synthetic approaches are discussed to introduce the phosphonate moieties into vinyl monomers, focusing especially on recent advances. Allyl-type, vinyl-type, styrenic-type and (meth)acrylic-type monomers bearing phosphonate groups (i.e. either mono or bisphosphonate) are considered with a special care about their reactivity in free radical (co)polymerization. It is shown that depending on the position of the phosphonate moieties the reactivity of the vinyl monomers is thus modified. For instance, free radical polymerization of vinyl phosphonate monomers is mainly dominated by transfer reactions, whereas the propagation rate of para-vinylbenzyl phosphonate monomers is enhanced by the phosphonate group. According to the structure of the phosphonate-bearing (co)polymers, the resulting properties are also investigated.