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A comparative study of different metal acetylacetonates covalently anchored onto amine functionalized silica: a study of the oxidation of aldehydes and alcohols to corresponding acids in water

Author
SODHI, Ravinderpal Kour1 ; PAUL, Satya1 ; CLARK, J. H2
[1] Department of Chemistry, University of Jammu, Jammu-180 006, India
[2] Green Chemistry Centre of Excellence, Department of Chemistry, University of York, Heslington, York, United Kingdom
Source

Green chemistry (Print). 2012, Vol 14, Num 6, pp 1649-1656, 8 p ; ref : 12 ref

ISSN
1463-9262
Scientific domain
Organic chemistry
Publisher
Royal Society of Chemistry, Cambridge
Publication country
United Kingdom
Document type
Article
Language
English
Keyword (fr)
Acide carboxylique Activité catalytique Acétylacétone Air Alcool benzylique Aldéhyde Amine Caractérisation Catalyse hétérogène Catalyseur Complexation Complexe de cobalt Complexe de cuivre Complexe de palladium Composé aromatique Coordinat organique Eau Enaldéhyde Etude comparative Fonctionnalisation Hétérocycle Manganèse Complexe Milieu aqueux Métal Complexe Oxydant Oxydation Oxyde de silicium Recyclage Ruthénium Complexe Réaction catalytique Silice Solution aqueuse Spectrométrie IR Spectrométrie absorption atomique Synthèse chimique Thermogravimétrie Transformation Fourier Propane(2-hydroperoxy-2-méthyl) SiO2 Métal transition Complexe Platinoïde Complexe
Keyword (en)
Carboxylic acid Catalyst activity Acetylacetone Air Benzyl alcohol Aldehyde Amine Characterization Heterogeneous catalysis Catalyst Complexation Cobalt complex Copper complex Palladium complex Aromatic compound Organic ligand Water Enaldehyde Comparative study Functionalization Heterocyclic compound Manganese Complexes Aqueous medium Metal Complexes Oxidant Oxidation Silicon oxides Recycling Ruthenium Complexes Catalytic reaction Silica Aqueous solution Infrared spectrometry Atomic absorption spectrometry Chemical synthesis Thermogravimetry Fourier transformation 2-Hydroperoxy-2-methyl-propane Transition metal Complexes Platinoid Complexes
Keyword (es)
Acido carboxílico Actividad catalítica Acetilacetona Aire Alcohol bencílico Aldehído Amina Caracterización Catálisis heterogénea Catalizador Complexación Cobalto complejo Cobre complejo Paladio complejo Compuesto aromático Ligando orgánico Agua Enaldehido Estudio comparativo Funciónalización Heterociclo Manganeso Complejo Medio acuoso Metal Complejo Oxidante Oxidación Reconversión Rutenio Complejo Reacción catalítica Sílice Solución acuosa Espectrometría IR Espectrometría absorción atómica Síntesis química Termogravimetría Transformación Fourier Metal transición Complejo Platinoide Complejo
Classification
Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01A Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry / 001C01A03 Catalysis / 001C01A03A Catalysts: preparations and properties

Pascal
001 Exact sciences and technology / 001C Chemistry / 001C01 General and physical chemistry / 001C01A Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry / 001C01A03 Catalysis / 001C01A03B Catalytic reactions

Pascal
001 Exact sciences and technology / 001C Chemistry / 001C02 Inorganic chemistry and origins of life / 001C02B Preparations and properties / 001C02B04 Coordination compounds

Pascal
001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C03 Noncondensed benzenic compounds

Discipline
General chemistry and physical chemistry Mineral chemistry and origin of life Organic chemistry
Origin
Inist-CNRS
Database
PASCAL
INIST identifier
26030251

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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