
Anne-Sophie Chauvin
+41 21 693 98 24
Office: BCH 3314
EPFL › SB › ISIC › LCS
Site web: https://lcs.epfl.ch
+41 21 693 98 24
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Site web: https://www.epfl.ch/schools/sb/scgc/
EPFL SB SCGC-GE
CP1 268 (Amphipole UNIL)
Rte de la Sorge
1015 Lausanne
+41 21 693 98 24
Office: CP1 268
EPFL › SB › SB-SCGC › SCGC-GE
Site web: https://www.epfl.ch/schools/sb/scgc/
+41 21 693 98 24
EPFL › SB › SB-DEC › CF-SB
Site web: https://sb.epfl.ch/conseil
Mission
In parallel, she is also developing palladium-based metallacages, further expanding her interest in the construction of functional supramolecular architectures through coordination-driven self-assembly.
She is teaching General and Analytical Chemistry to first-year Pharmacy and Biology students at UNIL, and overseeing practical sessions for students in chemistry, pharmacy, and biology.
She is elected at the FSB Faculty Council and was member of the EPFL Assembly (AE) for 6 years, until 2018. She was member of the Management committee of the Cost CM 1006 action entitled Eufen: European F-Element Network and Fellow of the Royal Society of Chemistry (FRSC). She is Member of the Swiss Chemical Society (SCS).
Alumni
Dr Julien Andrès
Dr Aurélien Willauer
Dr Andrei Andreichenko
Accessing Carbon, Boron and Germanium Spiro Stereocentres in a Unified Catalytic Enantioselective Approach
NATURE CATALYSIS. 2025. DOI : 10.1038/s41929-025-01352-3.Peptide‐Carbazolyl Cyanobenzene Conjugates: Enabling Biomolecule Functionalization via Photoredox and Energy Transfer Catalysis
Angewandte Chemie. 2025. DOI : 10.1002/ange.202507602.Coordination polymers: from uranium(IV) and thorium(IV) to non-uranyl U(V) and U(VI)
Lausanne, EPFL, 2025. DOI : 10.5075/epfl-thesis-11189.Peptide-Carbazolyl Cyanobenzene Conjugates: Enabling Biomolecule Functionalization via Photoredox and Energy Transfer Catalysis
2024Multielectron Redox Chemistry of Uranium by Accessing the plus II Oxidation State and Enabling Reduction to a U(I) Synthon
Journal Of The American Chemical Society. 2023. DOI : 10.1021/jacs.3c05626.Uranium(IV) and Thorium(IV) Coordination Polymers Based on Tritopic Carboxylic Acids
Inorganic Chemistry. 2023. DOI : 10.1021/acs.inorgchem.3c00881.Design Principles for the Development of Gd(III) Polarizing Agents for Magic Angle Spinning Dynamic Nuclear Polarization
Journal Of Physical Chemistry C. 2022. DOI : 10.1021/acs.jpcc.2c01721.Structure, reactivity and luminescence studies of triphenylsiloxide complexes of tetravalent lanthanides
Chemical Science. 2022. DOI : 10.1039/d1sc05517h.Stabilizing Unusual Oxidation States of Lanthanides in Molecular Complexes: Synthesis, Properties, and Reactivity
Lausanne, EPFL, 2022. DOI : 10.5075/epfl-thesis-9294.Synthesis and Characterization of Water Stable Uranyl(V) Complexes
Angewandte Chemie International Edition. 2021. DOI : 10.1002/anie.202016123.Vascular-targeted micelles as a specific MRI contrast agent for molecular imaging of fibrin clots and cancer cells
European Journal Of Pharmaceutics And Biopharmaceutics. 2021. DOI : 10.1016/j.ejpb.2020.11.017.Colorimetry of Luminescent Lanthanide Complexes
Molecules. 2020. DOI : 10.3390/molecules25174022.A Factor Two Improvement in High-Field Dynamic Nuclear Polarization from Gd(III) Complexes by Design
Journal Of The American Chemical Society. 2019. DOI : 10.1021/jacs.9b03723.Lanthanides in Solar Energy Conversion
Handbook on the Physics and Chemistry of Rare Earths; Amsterdam: Elsevier Science B.V., 2014. p. 169 - 281.Editorial - Solar Energy Harvesting
Chimia. 2013.Synthesis and cell localization of self-assembled dinuclear lanthanide bioprobes
Philosophical Transactions Of The Royal Society A-Mathematical Physical And Engineering Sciences. 2013. DOI : 10.1098/rsta.2012.0295.Energy transfer in coumarin-sensitised lanthanide luminescence: investigation of the nature of the sensitiser and its distance to the lanthanide ion
Physical Chemistry Chemical Physics. 2013. DOI : 10.1039/c3cp52279b.New sensitizers for dye-sensitized solar cells featuring a carbon-bridged phenylenevinylene
Chemical Communications (ChemComm). 2013. DOI : 10.1039/c2cc37124c.From Luminescent Lanthanide Complexes to Color Reproduction and Optical Document Security with Invisible Luminescent Inks
Lausanne, EPFL, 2012. DOI : 10.5075/epfl-thesis-5605.6-Phosphoryl Picolinic Acids as Europium and Terbium Sensitizers
Inorganic Chemistry. 2011. DOI : 10.1021/ic200983y.Lighting-up cancerous cells and tissues with lanthanide luminescence
CHIMIA. 2011. DOI : 10.2533/chimia.2011.361.Multiphoton-Excited Luminescent Lanthanide Bioprobes: Two- and Three-Photon Cross Sections of Dipicolinate Derivatives and Binuclear Helicates
The Journal of Physical Chemistry B. 2010. DOI : 10.1021/jp9090206.Europium Complexes of Tris(dipicolinato) Derivatives Coupled to Methylumbelliferone: A Double Sensitization
European Journal Of Inorganic Chemistry. 2010. DOI : 10.1002/ejic.201000126.Lanthanide luminescence efficiency in eight- and nine-coordinate complexes: Role of the radiative lifetime
Coordination Chemistry Reviews. 2010. DOI : 10.1016/j.ccr.2010.04.002.Bioconjugated lanthanide luminescent helicates as multilabels for lab-on-a-chip detection of cancer biomarkers
Analyst. 2010. DOI : 10.1039/b922124g.Sensitized near-IR luminescence of lanthanide complexes based on push-pull diketone derivatives
Dalton Transactions. 2010. DOI : 10.1039/b915893f.Increasing the efficiency of lanthanide luminescent bioprobes: bioconjugated silica nanoparticles as markers for cancerous cells
New Journal Of Chemistry. 2010. DOI : 10.1039/c0nj00440e.Luminescent Bimetallic Lanthanide Bioprobes for Cellular Imaging with Excitation in the Visible-Light Range
Chemistry - A European Journal. 2009. DOI : 10.1002/chem.200801868.Luminescent Lanthanide Helicates Self-Assembled from Ditopic Ligands Bearing Phosphonic Acid or Phosphoester Units
Inorganic Chemistry. 2009. DOI : 10.1021/ic901424w.Effect of the length of polyoxyethylene substituents on luminescent bimetallic lanthanide bioprobes
New Journal of Chemistry. 2008. DOI : 10.1039/b800516h.A versatile method for quantification of DNA and PCR products based on time-resolved EuIII luminescence
Analyst. 2008. DOI : 10.1039/b807959e.Remarkable Tuning of the Photophysical Properties of Bifunctional Lanthanide tris(Dipicolinates) and its Consequence on the Design of Bioprobes
Inorganic Chemistry. 2008. DOI : 10.1021/ic800842f.Synthesis of octa(1,1,3,3-tetramethylbutyl)octakis (dimethylphosphinoylmethyleneoxy)calix[8]arene and its application in the synergistic solvent extraction and separation of lanthanoids
Separation And Purification Technology. 2008. DOI : 10.1016/j.seppur.2008.09.011.Lanthanide Bimetallic Helicates for in Vitro Imaging and Sensing
Annals of the New York Academy of Sciences. 2008. DOI : 10.1196/annals.1430.010.Autoxidation of a 4-iminoimidazolidin-2-one with a tertiary 5-hydrogen to its 5-hydroxy derivative
Arkivoc. 2008. DOI : 10.3998/ark.5550190.0009.b02.A Versatile Ditopic Ligand System for Sensitizing the Luminescence of Bimetallic Lanthanide Bio-Imaging Probes
Chemistry - A European Journal. 2008. DOI : 10.1002/chem.200701357.Time-resolved luminescence microscopy of bimetallic lanthanide helicates in living cells
Org. Biomol. Chem.. 2008. DOI : 10.1039/b811427g.Luminescent lanthanides bioprobes emitting in the visible and/or near-infrared ranges
Lausanne, EPFL, 2008. DOI : 10.5075/epfl-thesis-4052.New Opportunities for Lanthanide Luminescence
Journal of Rare Earths. 2007. DOI : 10.1016/S1002-0721(07)60420-7.Non-Cytotoxic, Bifunctional EuIII and TbIII Luminescent Macrocyclic Complexes for Luminescence Resonant Energy- Transfer Experiments
Chemistry - A European Journal. 2007. DOI : 10.1002/chem.200700819.Luminescent lanthanide bimetallic triple-stranded helicates as potential cellular imaging probes
Chemical Communications (ChemComm). 2007. DOI : 10.1039/B701482A.Lanthanide Complexes with a Calix[8]arene Bearing Phosphinoyl Pendant Arms
European Journal of Inorganic Chemistry. 2007. DOI : 10.1002/ejic.200601180.Synthesis and characterization of partially substituted at lower rim phosphorus containing calix(4)arenes
Supramolecular Chemistry. 2007. DOI : 10.1080/10610270601105703.A Polyoxyethylene-Substituted Bimetallic Europium Helicate for Luminescent Staining of Living Cells
Chemistry - A European Journal. 2007. DOI : 10.1002/chem.200700883.Exploring the potential of europium(III) luminescence for the detection of phase transitions in ionic liquid crystals
Journal of Materials Chemistry. 2007. DOI : 10.1039/b614036j.Fluorinated β-Diketones for the Extraction of Lanthanide Ions: Photophysical Properties and Hydration Numbers of Their EuIII Complexes
European Journal of Inorganic Chemistry. 2006. DOI : 10.1002/ejic.200500849.Stable 8-hydroxyquinolinate-based podates as efficient sensitizers of lanthanide near-infrared luminescence
Inorganic chemistry. 2006. DOI : 10.1021/ic0515249.Use of Dipicolinate-Based Complexes for Producing Ion-Imprinted Polystyrene Resins for the Extraction of Yttrium-90 and Heavy Lanthanide Cations
Chemistry - A European Journal. 2006. DOI : 10.1002/chem.200501370.Lanthanide 8-hydroxyquinoline-based podates with efficient emission in the NIR range
Chemical Communications (ChemComm). 2005. DOI : 10.1039/B416575F.Influence of Anionic Functions on the Coordination and Photophysical Properties of Lanthanide(III) Complexes with Tridentate Bipyridines
Inorganic Chemistry. 2004. DOI : 10.1021/ic049118x.Cobalt(II), nickel(II), copper(II), and zinc(II) complexes with a p-tert-butylcalix[4]arene fitted with phosphinoyl pendant arms
European Journal of Inorganic Chemistry. 2004. DOI : 10.1002/ejic.200300858.Europium and Terbium tris(Dipicolinates) as Secondary Standards for Quantum Yield Determination
Spectroscopy Letters. 2004. DOI : 10.1081/SL-120039700.Tuning the keto equilibrium in 4-substituted dipicolinic acid derivatives
Organic & Biomolecular Chemistry. 2003. DOI : 10.1039/b211267c.General chemistry for students enrolled in a life sciences curriculum
CHIMIA. 2003. DOI : 10.2533/000942903777679587.Self-assembled triple-stranded lanthanide dimetallic helicates with a ditopic ligand derived from bis(benzimidazole)pyridine and featuring an (4-isothiocyanatophenyl)ethynyl substituent
Helvetica Chimica Acta. 2002. DOI : 10.1002/1522-2675(200207)85:7<1915::AID-HLCA1915>3.0.CO;2-N.A new versatile methodology for the synthesis of 4-halogenated 6-diethylcarbamoylpyridine-2-carboxylic acids
Tetrahedron Letters. 2001. DOI : 10.1016/S0040-4039(01)00392-6.A dirigé les thèses EPFL de
Julien Alexandre Andres, Steve Comby, Aurélien René Willauer, Andrei Andreichenko
Cours
Chimie TP I
The student will learn how to work in a chemistry laboratory. He/she will acquire a quantitative and/or qualitative approach. TP carried out are in relation to the courses of chemistry and will be followed by a second part "TP2".
Chimie générale et analytique I (TP pour PHA)
The objective of these practical works is to familiarize the student one with the techniques of basic manipulations and with the classical and instrumental methods of analysis. The laboratory work are also an illustration of the concepts described in the courses of general analytical Chemitry I+ II
Approfondissements en chimie analytique (pour PHA)
This course is complementary to the course entitled general and analytical chemistry II (UNIL 102) for biologists and pharmacists. It is given only to the students of pharmacy. It makes it possible to go further in analytical chemistry.
Chimie générale et analytique II (TP pour PHA)
These practical works are the continuation of the practical works TP I given to the fall semester
Chimie générale et analytique I (pour BIO+PHA)
To acquire the basic concepts to understand the impact of chemistry for a biologist or a pharmacist, in particular with regard to the comprehension of the essential phenomena of the Life (breathing, cellular activities)
Chimie générale et analytique I (TP pour BIO)
The objective of these practical works is to familiarize the student one with the techniques of basic manipulations and with the classical and instrumental methods of analysis. The laboratory work are also an illustration of the concepts described in the courses of general analytical Chemitry I+ II
Chimie TP II
Introduction to basic manipulations in general, inorganic and analytical chemistry. Introduction to classical quantitative analysis. Learn to carry out quantitative analysis. General principles of the classical quantitative analysis.
Chimie générale et analytique II (pour BIO+PHA)
This formation is in continuation to the course "General Chemistry I". It aims to give to the biologists and pharmacists a broad knowledge on chemistry and at applying the basic concepts previously acquired.