Laurent Plasseraud

Dr. Laurent Plasseraud

orcid

Research Focus & Metrics

Academic Career Length

32Years (1995-Present)

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

Representative Publications

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1 June 2006 in Catalysis Today
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Journal Article
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DBDanielle Ballivet-Tkatchenko
Danielle Ballivet-Tkatchenko
SCStéphane Chambrey
Stéphane Chambrey
RKRiitta Keiski
Riitta Keiski
RLRosane Ligabue
Rosane Ligabue
Laurent PlasseraudLaurent Plasseraud
Laurent Plasseraud
HTHelka Turunen
Helka Turunen

25 July 2019 in ACS Sustainable Chemistry & Engineering
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Journal Article
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SPSylvie Pourchet
Sylvie Pourchet
Rodolphe SonnierRodolphe Sonnier
Rodolphe Sonnier
MBMarwa Ben-Abdelkader
Marwa Ben-Abdelkader
YGYves Gaillard
Yves Gaillard
QRQuentin Ruiz
Quentin Ruiz
GBGilles Boni
Gilles Boni

14 August 2009 in Advanced Synthesis & Catalysis
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Journal Article
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PNPrashant U. Naik
Prashant U. Naik
LPLaetitia Petitjean
Laetitia Petitjean
KRKarima Refes
Karima Refes
MPMichel PICQUET
Michel PICQUET
Laurent PlasseraudLaurent Plasseraud
Laurent Plasseraud

17 September 2001 in Chemistry – A European Journal
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Journal Article
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Laurent PlasseraudLaurent Plasseraud
Laurent Plasseraud
HMHarald Maid
Harald Maid
FHFrank Hampel
Frank Hampel
RSRolf W. Saalfrank
Rolf W. Saalfrank

11 April 2012 in Polymer Chemistry
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Journal Article
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PNPrashant U. Naik
Prashant U. Naik
KRKarima Refes
Karima Refes
FSFaten Sadaka
Faten Sadaka
CBClaire-Hélène Brachais
Claire-Hélène Brachais
GBGilles Boni
Gilles Boni
Laurent PlasseraudLaurent Plasseraud
Laurent Plasseraud
A new efficient and expeditious route to the synthesis of aliphatic polycarbonates, in solvent-free conditions and using 1-n-butyl-3-methylimidazolium-2-carboxylate (BMIM-2-CO2) as a catalyst precursor, is described. The protocol consists of a two-step polymerization process involving the transesterification of dimethyl carbonate (DMC) with linear alkane diols and leading to high molecular weight homopolymers. The reaction went to completion quantitatively with the liberation of methanol as the only by-product. The in situ formation of N-heterocyclic carbene species resulting from BMIM-2-CO2 decarboxylation is suggested to be a key feature of the condensation process. The protocol was then applied to the copolymerization of diverse diols leading to the synthesis of polycarbonates with average segment lengths and random sequences.

1 November 2003 in Applied Catalysis A: General
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Journal Article
Closed access
DBDanielle Ballivet-Tkatchenko
Danielle Ballivet-Tkatchenko
TJThomas Jerphagnon
Thomas Jerphagnon
RLRosane Ligabue
Rosane Ligabue
Laurent PlasseraudLaurent Plasseraud
Laurent Plasseraud
DPDidier Poinsot
Didier Poinsot