Locking of helicity and shape complementarity in diarylethene dimers on graphite.

Locking of helicity and shape complementarity in diarylethene dimers on graphite. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

Locking of helicity and shape complementarity in diarylethene dimers on graphite. Abstract Text:

Nathalie Katsonis,Andrea Minoia,Tibor Kudernac,Toshiki Mutai,Hong Xu,Hiroshi Uji-I,Roberto Lazzaroni,Steven De Feyter,Ben L Feringa,Nathalie Katsonis,Andrea Minoia,Tibor Kudernac,Toshiki Mutai,Hong Xu,Hiroshi Uji-I,Roberto Lazzaroni,Steven De Feyter,Ben L Feringa,

Locking of helicity and shape complementarity in diarylethene dimers on graphite. Publishing Authors By Initials

N Katsonis,A Minoia,T Kudernac,T Mutai,H Xu,H Uji-I,R Lazzaroni,SD Feyter,BL Feringa,N Katsonis,A Minoia,T Kudernac,T Mutai,H Xu,H Uji-I,R Lazzaroni,SD Feyter,BL Feringa,

For similar abstracts research abstracts see: abstracts research

PUBMED ID PMID:

MEDLINE DATE:

Locking of helicity and shape complementarity in diarylethene dimers on graphite. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: Journal of the American Chemical Society

VOLUME: 130

Page Numbers: 386-7

Journal Abbreviation: J. Am. Chem. Soc.

ISSN: 1520-5126

DAY: 21

MONTH: 12

YEAR: 2007

Locking of helicity and shape complementarity in diarylethene dimers on graphite. Information

Number of References:

LANGUAGE: eng

NlmUniqueID: 7503056

Locking of helicity and shape complementarity in diarylethene dimers on graphite. Keywords Mesh Terms:

KEYWORDS:

MESH TERMS:

Chemical & Substance for Abstract: Locking of helicity and shape complementarity in diarylethene dimers on graphite. Information

Substance Name:

Registry Number:

Grant and Affiliation Information for Locking of helicity and shape complementarity in diarylethene dimers on graphite.

AFFILIATION: Department of Organic and Molecular Inorganic Chemistry, Stratingh Institute, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands. N.H.Katsonis@rug.nl

Country: United States

AGENCY:

GRANT:

ACRONYM:

MEDLINETA: J Am Chem Soc

REFSOURCE:

DATABASENAME:

ACCESSION NUMBER:

Number Hits: 0

Locking of helicity and shape complementarity in diarylethene dimers on graphite Related Publications

• A highly enantioselective intramolecular Heck reaction with a monodentate ligand.
• A redesign of light-driven rotary molecular motors.
• Acceleration of a nanomotor: electronic control of the rotary speed of a light-driven molecular rotor.
• An iterative catalytic route to enantiopure deoxypropionate subunits: asymmetric conjugate addition of grignard reagents to alpha,beta-unsaturated thioesters.
• Autonomous movement of silica and glass micro-objects based on a catalytic molecular propulsion system.
• Autonomous propulsion of carbon nanotubes powered by a multienzyme ensemble.
• Catalytic asymmetric conjugate addition and allylic alkylation with grignard reagents.
• Catalytic enantioselective Reformatsky reaction with ketones.
• Catalytic enantioselective addition of organometallic reagents to N-formylimines using monodentate phosphoramidite ligands.
• Catalytic enantioselective reformatsky reaction with aldehydes.
• Copper-catalyzed enantioselective conjugate addition of grignard reagents to acyclic enones.
• Darvon and the EEG.
• De novo asymmetric bio- and chemocatalytic synthesis of saccharides - stereoselective formal O-glycoside bond formation using palladium catalysis.
• Dynamic chiral selection and amplification using photoresponsive organogelators.
• Following the autonomous movement of silica microparticles using fluorescence microscopy.
• Highly enantioselective rhodium-catalyzed hydrogenation of beta-dehydroamino acid derivatives using monodentate phosphoramidites.
• Highly versatile enantioselective conjugate addition of Grignard reagents to alpha,beta-unsaturated thioesters.
• Intramolecular energy transfer in a tetra-coumarin perylene system: influence of solvent and bridging unit on electronic properties.
• Light-controlled supramolecular helicity of a liquid crystalline phase using a helical polymer functionalized with a single chiroptical molecular switch.
• Locking of helicity and shape complementarity in diarylethene dimers on graphite.
• MHz unidirectional rotation of molecular rotary motors.
• Macroscopic expression of the chirality of amino alcohols by a double amplification mechanism in liquid crystalline media.
• Making molecular machines work.
• Manganese catalysed asymmetric cis-dihydroxylation with H(2)O(2).
• On the effect of donor and acceptor substituents on the behaviour of light-driven rotary molecular motors.
• Photoresponsive dithienylethene-urea-based organogels with "reversed" behavior.
• Photoresponsive rolling and bending of thin crystals of chiral diarylethenes.
• Pre-operative risk assessment and risk reduction before surgery.
• Straightforward synthesis of alpha,beta-unsaturated thioesters via ruthenium-catalyzed olefin cross-metathesis with thioacrylate.
• Tuning energy transfer in switchable donor-acceptor systems.