dc.creatorTorviso, Maria del Rosario
dc.creatorMansilla, Daniela Soledad
dc.creatorBelizán, A.
dc.creatorAlesso, E.
dc.creatorMoltrasio, Graciela Yolanda
dc.creatorVazquez, Patricia Graciela
dc.creatorPizzio, Luis Rene
dc.creatorBlanco, Mirta Noemi
dc.creatorCaceres, Carmen Victoria
dc.date.accessioned2018-10-18T14:48:48Z
dc.date.accessioned2018-11-06T12:01:06Z
dc.date.available2018-10-18T14:48:48Z
dc.date.available2018-11-06T12:01:06Z
dc.date.created2018-10-18T14:48:48Z
dc.date.issued2008-04
dc.identifierTorviso, Maria del Rosario; Mansilla, Daniela Soledad; Belizán, A.; Alesso, E.; Moltrasio, Graciela Yolanda; et al.; Catalytic activity of Keggin heteropolycompounds in the Pechmann reaction; Elsevier Science; Applied Catalysis A: General; 339; 1; 4-2008; 53-60
dc.identifier0926-860X
dc.identifierhttp://hdl.handle.net/11336/62695
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1862309
dc.description.abstractDifferent heteropolycompounds were used as catalysts in the synthesis of coumarins from phenols and ethyl acetoacetate. The H3PMo12O40 and H3PW12O40 Keggin heteropolyacids were supported on different types of silica. On the other hand, the aluminium salts of these heteropolyacids and that of the H4SiW12O40 acid were prepared. The specific surface area (SBET), and the mean pore diameter of the obtained catalysts were estimated from the adsorption isotherms of nitrogen at 77 K. Their Fourier transform infrared spectra were recorded and their acidity was determined by potentiometric titration with a solution of n-butylamine in acetonitrile. The catalytic activity using several phenols such as resorcinol, 3,5-dimethoxyphenol, a-naphtol and b-naphtol were determined. High yield of product was obtained in the case of 4-methyl-7-hydroxycoumarin (80–95%), 4-methyl-5,7-dimethoxycoumarin (60–92%) and 4-methyl-7,8-benzocoumarin (90%). However, the 4-methyl-5,6- benzocoumarin yield was low. The use of microwave radiation as power source increases the reaction yield and mainly decreases the reaction time.
dc.languageeng
dc.publisherElsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1016/j.apcata.2008.01.020
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0926860X08000331
dc.rightshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectCATALYSTS
dc.subjectKEGGIN HETEROPOLYCOMPOUNDS
dc.subjectPECHMANN REACTION
dc.titleCatalytic activity of Keggin heteropolycompounds in the Pechmann reaction
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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