Photocontrolled Molecular Assembler Based on Cucurbit[8]uril: [2+2]-Autophotocycloaddition of Styryl Dyes in the Solid State and in Water
- Author
- GROMOV, Sergey P1 ; VEDERNIKOV, Artem I1 ; KUZ'MINA, Lyudmila G2 ; KONDRATUK, Dmitry V1 ; SAZONOV, Sergey K1 ; STRELENKO, Yuri A3 ; ALFIMOV, Michael V1 ; HOWARD, Judith A. K4
[1] Photochemistry Centre, Russian Academy of Sciences, Novatorov str. 7A-1, Moscow 119421, Russian Federation
[2] N. S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Leninskiy prosp. 31, Moscow 119991, Russian Federation
[3] N. D. Zelinskiy Institute of Organic Chemistry, Russian Academy of Sciences, Leninskiy prosp. 47, Moscow 119991, Russian Federation
[4] Chemistry Department, Durham University, South Road, Durham DH1 3LE, United Kingdom - Source
European journal of organic chemistry (Print). 2010, Num 13, pp 2587-2599, 13 p ; ref : 17 ref
- ISSN
- 1434-193X
- Scientific domain
- Organic chemistry
- Publisher
- Wiley-VCH, Weinheim
- Publication country
- Germany
- Document type
- Article
- Language
- Russian
- Author keyword
- Cavitands Cycloaddition Dyes/Pigments Host-guest systems Molecular devices Photochemistry
- Keyword (fr)
- Acétonitrile Assemblage moléculaire Bétaïnes Colorant Composé inclusion Cycloaddition Cyclophane Diffraction RX Dimère Dérivé de la pyridine Dérivé du cyclobutane Dérivé du styrène Eau Etat solide Hydrogène 1 Hétérocycle azote Irradiation Macrocycle Photochimie Photoisomérisation Pigment Pyridine Rigidité moléculaire Solution aqueuse Solution chimique Spectrométrie RMN Spectrométrie UV visible Stabilité Stoechiométrie Structure cristalline Structure moléculaire Stéréospécificité Synthèse chimique Cavitand Cucurbiturile Deutérium Oxyde Pseudorotaxane
- Keyword (en)
- Acetonitrile Molecular assembly Betaines Dyes Inclusion compound Cycloaddition Cyclophane X ray diffraction Dimer Pyridine derivatives Cyclobutane derivatives Styrene derivatives Water Solid state Hydrogen 1 Nitrogen heterocycle Irradiation Macrocycle Photochemistry Photoisomerization Pigments Pyridine Molecular rigidity Aqueous solution Chemical solution NMR spectrometry Ultraviolet visible spectrometry Stability Stoichiometry Crystalline structure Molecular structure Stereospecificity Chemical synthesis Cavitand
- Keyword (es)
- Acetonitrilo Ensamble molecular Betainas Colorante Compuesto inclusión Cicloadición Ciclofano Difracción RX Dímero Piridina derivado Ciclobutano derivado Estireno derivado Agua Estado sólido Heterociclo nitrógeno Irradiación Macrociclo Fotoquímica Fotoisomerización Pigmento Piridina Rigidez molecular Solución acuosa Solución química Espectrometría RMN Espectrometría UV visible Estabilidad Estequiométría Estructura cristalina Estructura molecular Estereoespecificidad Síntesis química
- Classification
- Pascal
- 001 Exact sciences and technology / 001B Physics / 001B80 Cross-disciplinary physics: materials science; rheology / 001B80A Materials science / 001B80A16 Methods of nanofabrication / 001B80A16F Supramolecular and biochemical assembly
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C05 Alicyclic compounds, terpenoids, prostaglandins, steroids / 001C03C05A Alicyclic compounds
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C06 Heterocyclic compounds / 001C03C06B Heterocyclic compounds with only one n hetero atom and condensed derivatives
- Discipline
- Organic chemistry Physics and materials science
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 22695740
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1002/ejoc.200901324 
https://dx.doi.org/10.1002/ejoc.200901324
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