Jerome Husson

Dr. Jerome Husson

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Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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15 February 2010 in Chemistry – A European Journal
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Journal Article
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SCStefano Caramori
Stefano Caramori
JHJerome Husson
Jerome Husson
MBMarc Beley
Marc Beley
CBCarlo Alberto Bignozzi
Carlo Alberto Bignozzi
RARoberto Argazzi
Roberto Argazzi
Philippe C. GrosPhilippe C. Gros
Philippe C. Gros

1 July 2005 in Inorganica Chimica Acta
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Journal Article
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MBM. Beley
M. Beley
DDD. Delabouglise
D. Delabouglise
GHG. Houppy
G. Houppy
JHJerome Husson
Jerome Husson
JPJ.-P. Petit
J.-P. Petit

1 May 2012 in Journal of Heterocyclic Chemistry
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Journal Article
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JHJerome Husson
Jerome Husson
Michael KnorrMichael Knorr
Michael Knorr

1 May 2012 in Colloids and Surfaces B: Biointerfaces
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Journal Article
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RSRattiya Singhon
Rattiya Singhon
JHJerome Husson
Jerome Husson
Michael KnorrMichael Knorr
Michael Knorr
Boris LakardBoris Lakard
Boris Lakard
MEMyriam Euvrard
Myriam Euvrard

12 March 2012 in Beilstein Journal of Organic Chemistry
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JHJerome Husson
Jerome Husson
Michael KnorrMichael Knorr
Michael Knorr
Different synthetic routes leading to terpyridines functionalised with furan heterocycles are reviewed. The methodologies used to prepare such compounds include the ring closure of 1,5-diketones and cross-coupling reactions. These versatile terpyridines and their derived metal complexes find applications in various fields including coordination chemistry, medicinal chemistry and material sciences.

26 October 2011 in Green Chemistry
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JDJérémy Dehaudt
Jérémy Dehaudt
JHJerome Husson
Jerome Husson
LGLaurent Guyard
Laurent Guyard
We report in this paper a new route for the synthesis of 4,4′,4′′-tricarboxy-2,2′:6′,2′′-terpyridine. This synthetic pathway has a lower ecological impact with respect to yield, atom economy, solvent and chemicals used and wastes generated when compared to a previously reported method. In addition it uses furfural, which can be obtained from renewable sources. The title compound can be used to prepare complexes that are valuable for applications in Dye Sensitized Solar Cells.