James Fraser Stoddart
Stoddart, J. F.
Stoddart, J. F., 1942-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Stoddart, James Fraser 1942-
Stoddart, Fraser (1942- )
Stoddart, J. F. (James Fraser), 1942-
Stoddart, J. Fraser 1942-
Stoddart, J. Fraser
Stoddart, J. Fraser, chemicus
VIAF ID: 66526866 ( Personal )
Permalink: http://viaf.org/viaf/66526866
Preferred Forms
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100 0 _
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James Fraser Stoddart
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Stoddart
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J. F.
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200 _ 1 ‡a Stoddart ‡b James Fraser ‡f 1942-
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100 1 _ ‡a Stoddart, Fraser ‡d (1942- )
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100 1 _ ‡a Stoddart, J. F.
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Stoddart, J. F.
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100 1 0
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Stoddart, J. F.
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100 1 _ ‡a Stoddart, J. F.
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Stoddart, J. F.
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1942-
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100 1 _ ‡a Stoddart, J. F. ‡q (James Fraser), ‡d 1942-
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100 1 _
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Stoddart, J. F.,
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1942-....
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100 1 _ ‡a Stoddart, J. Fraser
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100 1 _
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Stoddart, J. Fraser
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1942-
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100 1 _ ‡a Stoddart, J. Fraser, ‡c chemicus
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100 1 _ ‡a Stoddart, James Fraser ‡d (1942- ).
4xx's: Alternate Name Forms (57)
Works
| Title | Sources |
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| 2007 Tetrahedron prize for creativity in organic chemistry : synthetic nanosystems and nanomachinery, Professor Fraser Stoddart |
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| Comprehensive organic chemistry the synthesis and reactions of organic compounds |
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| nature of the mechanical bond from molecules to machines |
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| Obŝaâ organičeskaâ himiâ. |
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| Polyvalent scaffolds. Counting the number of seats available for eosin guest molecules in viologen-based host dendrimers. |
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| Polyviologen dendrimers as hosts and charge-storing devices. |
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| Porphyrinic supramolecular daisy chains incorporating pillar[5]arene–viologen host–guest interactions |
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| The power of click chemistry for molecular machines and surface patterning |
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| Preparation and Properties of Polymer-Wrapped Single-Walled Carbon Nanotubes We would like to acknowledge the following agencies and foundations for supporting various aspects of this work: the polymer synthesis and spectroscopic characterization of |
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| Probing Distance Dependent Charge-Transfer Character in Excimers of Extended Viologen Cyclophanes Using Femtosecond Vibrational Spectroscopy. |
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| Probing polyvalency in artificial systems exhibiting molecular recognition. |
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| Proton Conduction in Tröger’s Base-Linked Poly(crown ether)s |
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| Pseudorotaxanes and Rotaxanes Formed by Viologen Derivatives |
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| Putting mechanically interlocked molecules (MIMs) to work in tomorrow's world |
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| Quantifying the working stroke of tetrathiafulvalene-based electrochemically-driven linear motor-molecules. |
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| Quantitative emergence of hetero[4]rotaxanes by template-directed click chemistry. |
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| Quantum Mechanical and Experimental Validation that Cyclobis(paraquat-p-phenylene) Forms a 1:1 Inclusion Complex with Tetrathiafulvalene. |
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| A radically configurable six-state compound. |
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| Radically enhanced molecular switches. |
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| Radically promoted formation of a molecular lasso. |
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| Rapid thermally assisted donor-acceptor catenation |
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| Reactions under the click chemistry philosophy employed in supramolecular and mechanostereochemical systems. |
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| Recognition of Bipyridinium-Based Derivatives by Hydroquinone- and/or Dioxynaphthalene-Based Macrocyclic Polyethers: From Inclusion Complexes to the Self-Assembly of [2]Catenanes† |
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| Redox-Active Phenanthrenequinone Triangles in Aqueous Rechargeable Zinc Batteries |
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| Redox Control of the Binding Modes of an Organic Receptor. |
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| Redox-controllable amphiphilic [2]rotaxanes. |
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| Redox-controlled selective docking in a [2]catenane host. |
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| A redox-driven multicomponent molecular shuttle. |
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| Redox-driven switching in pseudorotaxanes |
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| A redox-switchable alpha-cyclodextrin-based [2]rotaxane. |
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| A Redox-Switchable Molecular Zipper |
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| Relative contractile motion of the rings in a switchable palindromic [3]rotaxane in aqueous solution driven by radical-pairing interactions. |
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| Relative unidirectional translation in an artificial molecular assembly fueled by light. |
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| Reticular Access to Highly Porous acs-MOFs with Rigid Trigonal Prismatic Linkers for Water Sorption |
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| A Reverse Donor-Acceptor Bistable [2]Catenane |
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| A reversible light-operated nanovalve on mesoporous silica nanoparticles. |
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| Reversing a rotaxane recognition motif: threading oligoethylene glycol derivatives through a dicationic cyclophane. |
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| Rigid-strut-containing crown ethers and [2]catenanes for incorporation into metal-organic frameworks. |
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| Robust dynamics. |
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| A self-assembled multivalent pseudopolyrotaxane for binding galectin-1. |
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| Self-assembly in the metallation of bis(aminoaryl) ethers |
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| Self-Assembly of a [2]Pseudorota[3]catenane in Water |
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| Self-Assembly of [n]Rotaxanes Bearing Dendritic Stoppers⊥ |
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| Self-assembly, stability quantification, controlled molecular switching, and sensing properties of an anthracene-containing dynamic [2]rotaxane. |
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| Self-assembly with block copolymers through metal coordination of SCS-Pd(II) pincer complexes and pseudorotaxane formation |
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| A self-complexing and self-assembling pillar[5]arene |
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| Semiconducting single crystals comprising segregated arrays of complexes of C60. |
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| Shuttling dynamics in an acid-base-switchable [2]rotaxane. |
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| Shuttling Rates, Electronic States, and Hysteresis in a Ring-in-Ring Rotaxane. |
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| Simple Mechanical Molecular and Supramolecular Machines: Photochemical and Electrochemical Control of Switching Processes |
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| Single-Crystal Polycationic Polymers Obtained by Single-Crystal-to-Single-Crystal Photopolymerization |
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| Single-walled carbon nanotubes under the influence of dynamic coordination and supramolecular chemistry. |
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| Size-Matched Radical Multivalency. |
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| Stereochemistry of carbohydrates |
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| Stereohimiă uglevodov |
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| Stimulating concepts in chemistry |
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| Switchable neutral bistable rotaxanes. |
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| Symbiotic Control in Mechanical Bond Formation. |
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| Synthesis and solution-state dynamics of donor–acceptor oligorotaxane foldamers |
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| Synthesis of biomolecule-modified mesoporous silica nanoparticles for targeted hydrophobic drug delivery to cancer cells. |
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| Synthesis of Ex(n)Box cyclophanes. |
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| Synthesis of Glycodendrimers by Modification of Poly(propylene imine) Dendrimers |
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| Synthesis of lactoside glycodendrons using photoaddition and reductive amination methodologies. |
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| Synthesis, structure, and metalation of two new highly porous zirconium metal-organic frameworks. |
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| Synthetic Cyclic Oligosaccharides-Syntheses and Structural Properties of a Cyclo[(1 → 4)-α-L-rhamnopyranosyl-(1 → 4)-α-D-mannopyranosyl]trioside and -tetraoside. |
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| Tayi et al. reply. |
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| Template-Directed One-Step Synthesis of Cyclic Trimers by ADMET |
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| Template-directed syntheses of rigid oligorotaxanes under thermodynamic control |
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| Template-directed synthesis employing reversible imine bond formation. |
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| Templated Synthesis of Interlocked Molecules |
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| Tetrathiafulvalene radical cation dimerization in a bistable tripodal [4]rotaxane. |
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| Tetrathiafulvalenenaphthalenophanes: Planar Chirality andcis/transPhotoisomerization |
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| TetrazineBox: A Structurally Transformative Toolbox |
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| Общая органическая химия : [в 12-ти т.] |
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| Стереохимия углеводов, 1975: |
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