Durola, Fabien, 1979-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Fabien Durola
VIAF ID: 213329250 (Personal)
Permalink: http://viaf.org/viaf/213329250
Preferred Forms
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100 1 _
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Durola, Fabien
‡d
1979-...
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100 1 _
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Durola, Fabien,
‡d
1979-....
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100 0 _
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Fabien Durola
4xx's: Alternate Name Forms (2)
5xx's: Related Names (2)
- 511 2 _
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Institut de génétique et de biologie moléculaire et cellulaire (Strasbourg)
- 511 2 _
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Université de Strasbourg (2009-....)
Works
| Title | Sources |
|---|---|
| Autour de nouveaux chélates:les 8,8'-diphényle-3,3'-biisoquinolines : Machines moléculaires rapides et nouvelles topologies |
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| A carboxyfunctionalized (24)-1,6-pyrenophane-tetraene by glyoxylic Perkin condensation |
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| Columnar Liquid-Crystalline Dibenzopentacenodithiophenes by Photocyclization |
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| Columnar Liquid-Crystalline Dinaphthoperylenetetracarboxdiimides |
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| Conception de nouvelles topologies moléculaires repliées et d'un hôte foldamère photocommutable |
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| Control of nanospaces with molecular devices |
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| A cyclic [4]rotaxane that behaves as a switchable molecular receptor: formation of a rigid scaffold from a collapsed structure by complexation with copper(I) ions |
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| Cyclic [4]Rotaxanes Containing Two Parallel Porphyrinic Plates: Toward Switchable Molecular Receptors and Compressors |
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| Cyclic tris-[5]helicenes with single and triple twisted Möbius topologies and Möbius aromaticity |
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| Cyclobishelicenes: Shape-Persistent Figure-Eight Aromatic Molecules with Promising Chiroptical Properties |
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| Design of new molecular folded topologies and of a photoswitchable foldamer host. |
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| Dipyreno- and diperyleno-anthracenes from glyoxylic Perkin reactions |
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| Distorted arene core allows room-temperature columnar liquid-crystal glass with minimal side chains |
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| Fast electrochemically induced translation of the ring in a copper-complexed [2]rotaxane: the biisoquinoline effect |
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| A fast-moving copper-based molecular shuttle: synthesis and dynamic properties. |
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| Formation of fully conjugated macrocycles by Perkin reactions. |
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| From Chrysene to Double [5]Helicenes |
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| Fused Helicene Chains: Towards Twisted Graphene Nanoribbons |
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| Helicenes from Diarylmaleimides |
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| Helicenic N-heterocyclic carbenes (helicenic NHCs) : synthesis and study of the physico-chemical and catalytic properties. |
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| Highly Twisted Arenes by Scholl Cyclizations with Unexpected Regioselectivity |
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| Iron(II)-templated synthesis of [3]rotaxanes by passing two threads through the same ring |
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| Isomeric Column-Forming Esters and Imides with Varying Curvatures of the Aromatic Plane |
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| Molécules chirales à géométrie hélicoïdale : synthèse et modulation de leurs propriétés spectroscopiques par leur environnement |
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| Monoprotection of Arylene-Diacetic Acids Allowing the Build-Up of Longer Aromatic Ribbons by Successive Perkin Condensations |
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| Near-infrared dual luminescence from an extended zinc porphyrin |
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| NIR emission of cyclic [4]rotaxanes containing π-extended porphyrin chromophores |
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| Non-planar oligoarylene macrocycles from biphenyl |
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| Nouvelles directions avec les cyclobutanones et les arynes exploitant l'organocatalyse énantiosélective. |
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| Plank-Shaped Column-Forming Mesogens with Substituents on One Side Only |
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| Polycyclic aromatic hydrocarbons and chirality : synthesis and modelisation. |
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| Quantitative formation of [4]pseudorotaxanes from two rods and two bis-macrocycles incorporating porphyrinic plates between the rings |
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| A rapidly shuttling copper-complexed [2]rotaxane with three different chelating groups in its axis |
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| Stabilization of the Columnar Mesophase of Perylenediimide by Racemic Triple Tails |
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| Sterically non-hindering endocyclic ligands of the bi-isoquinoline family |
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| Synthesis of Carboxy-Functionalized Polycyclic Arenes by Oxidative Cyclizations of 2,3-Diarylacrylates |
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| Techniques de protection pour la synthèse de larges arènes polycycliques par réaction de Perkin |
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| Three-Component Entanglements Consisting of Three Crescent-Shaped Bidentate Ligands Coordinated to an Octahedral Metal Centre |
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| Twisted polycyclic arenes by intramolecular Scholl reactions of C3-symmetric precursors |
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| Vers la synthèse de composés poly-hélicènes macrocycles topologiquement non triviaux. |
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