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http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_48/101021ja076570h/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_12/101021ja057664z/authorship/3
http://hub.abes.fr/edp/periodical/medsci/2013/volume_29/issue_5/medsci2013295p452/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2003/volume_125/issue_44/101021ja036665t/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_40/101021ja075219t/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_8/101021ja077223a/authorship/11
http://hub.abes.fr/acs/periodical/jpcbfk/2006/volume_110/issue_34/101021jp061836c/authorship/3
http://hub.abes.fr/acs/periodical/jpccck/2007/volume_111/issue_18/101021jp070463s/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/1999/volume_121/issue_17/101021ja9841310/authorship/3
http://hub.abes.fr/acs/periodical/jpcbfk/2001/volume_105/issue_44/101021jp011455t/authorship/8
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http://hub.abes.fr/acs/periodical/jpcafh/1998/volume_102/issue_29/101021jp973275i/authorship/3
http://hub.abes.fr/acs/periodical/jpcbfk/1999/volume_103/issue_46/101021jp991870/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/1997/volume_119/issue_45/101021ja971224t/authorship/2
http://hub.abes.fr/acs/periodical/jacsat/2008/volume_130/issue_6/101021ja7102394/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_45/101021ja015919c/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/2001/volume_123/issue_25/101021ja001697r/authorship/2
http://hub.abes.fr/acs/periodical/mamobx/2004/volume_37/issue_1/101021ma034680c/authorship/5
http://hub.abes.fr/acs/periodical/jacsat/2004/volume_126/issue_39/101021ja0484193/authorship/3
http://hub.abes.fr/acs/periodical/jacsat/2003/volume_125/issue_28/101021ja0352552/authorship/4
http://hub.abes.fr/acs/periodical/jacsat/2006/volume_128/issue_2/101021ja054886o/authorship/9
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_39/101021ja073513f/authorship/6
http://hub.abes.fr/acs/periodical/jpcbfk/2004/volume_108/issue_39/101021jp048621s/authorship/10
http://hub.abes.fr/acs/periodical/jpcbfk/2006/volume_110/issue_15/101021jp0561468/authorship/7
http://hub.abes.fr/acs/periodical/jacsat/2007/volume_129/issue_3/101021ja067410t/authorship/2
http://hub.abes.fr/acs/periodical/jpcbfk/2002/volume_106/issue_34/101021jp020338a/authorship/6
http://hub.abes.fr/acs/periodical/jacsat/1999/volume_121/issue_11/101021ja9815273/authorship/2
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http://hub.abes.fr/acs/periodical/jacsat/1999/volume_121/issue_7/101021ja983106r/authorship/2
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http://hub.abes.fr/acs/periodical/langd5/1995/volume_11/issue_7/101021la00007a001/authorship/1
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Second Harmonic Generation from Langmuir-Blodgett Films of Fullerene-Aza-Crown Ethers and Their Potassium Ion Complexes
High-Frequency Vibrations of the Simplest Benzylic Amide [2]Catenane
Solution and Solid-State Properties of Mechanically LinkedPolycarbonates
Switching “On” and “Off” the Expression of Chirality inPeptide Rotaxanes
Mechanically Linked Polycarbonate
Catalytic “Click” Rotaxanes: A Substoichiometric Metal-Template Pathway toMechanically Interlocked Architectures
Electrochemically Induced Dynamics of a Benzylic Amide [2]Catenane
Adsorption of Fumaramide [2]Rotaxane and Its Components on a Solid Substrate: ACoverage-Dependent Study
How Do Benzylic Amide [2]Catenane Rings Rotate?
The Effect of Mechanical Interlocking on Crystal Packing: Predictions and Testing
The Synthesis and Solubilization of AmideMacrocycles via Rotaxane Formation
Peptide-Based Molecular Shuttles
Organic “Magic Rings”: The HydrogenBond-Directed Assembly of Catenanes underThermodynamic Control
Stiff, and Sticky in the Right Places: The Dramatic Influence ofPreorganizing Guest Binding Sites on the Hydrogen Bond-DirectedAssembly of Rotaxanes
A Generic Basis for Some Simple Light-Operated Mechanical MolecularMachines
Catalytic “Active-Metal” Template Synthesis of [2]Rotaxanes,[3]Rotaxanes, and Molecular Shuttles, and SomeObservations on the Mechanism of the Cu(I)-CatalyzedAzide−Alkyne 1,3-Cycloaddition
Conformational Self-Recognition as the Origin of Dewetting in Bistable Molecular Surfaces
Grafting of Benzylic Amide Macrocycles onto Acid-Terminated Self-Assembled MonolayersStudied by XPS, RAIRS, and Contact Angle Measurements
http://hub.abes.fr/edp/periodical/medsci/2013/volume_29/issue_5/medsci2013295p452/w
Adsorption of a Benzylic Amide Macrocycle on a Solid Substrate: XPS and HREELSCharacterization of Thin Films Grown on Au(111)
A Chemically-Driven Molecular Information Ratchet
Surface Enhanced Second Harmonic Generation from Macrocycle, Catenane, and RotaxaneThin Films: Experiments and Theory
Controlling the Frequency of Macrocyclic Ring Rotation in BenzylicAmide [2]Catenanes
Selecting Topology and Connectivity through Metal-DirectedMacrocyclization Reactions: A Square Planar Palladium[2]Catenate and Two Noninterlocked Isomers
Rotaxanes of Cyclic Peptides
Enhanced Hydrogen Bonding Induced by OpticalExcitation: Unexpected SubnanosecondPhotoinduced Dynamics in a Peptide-Based[2]Rotaxane
Chiroptical Switching in a Bistable Molecular Shuttle
Beyond Switches: Ratcheting a Particle Energetically Uphillwith a Compartmentalized Molecular Machine
[2]Rotaxanes through Palladium Active-Template Oxidative HeckCross-Couplings
Three State Redox-Active Molecular Shuttle That Switches inSolution and on a Surface
Heterovibrational Interactions, Cooperative Hydrogen Bonding, and Vibrational EnergyRelaxation Pathways in a Rotaxane
Electrochemically Switchable Hydrogen-Bonded MolecularShuttles
Self-organization of Rotaxane Thin Films into SpatiallyCorrelated Nanostructures: Morphological and StructuralAspects
Extremely Strong and Readily Accessible AAA−DDD Triple Hydrogen BondComplexes
A Switchable Palladium-Complexed Molecular Shuttle and ItsMetastable Positional Isomers
Structural, Electrochemical, and Photophysical Properties of a Molecular Shuttle Attachedto an Acid-Terminated Self-Assembled Monolayer
“Smart” Rotaxanes: Shape Memory and Control in Tertiary AmidePeptido[2]rotaxanes
The in situ activation of thioglycosides with bromine: an improved glycosylation method
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