dc.creatorOliveira, Rafael de Lima
dc.creatorKiyohara, Pedro Kunihiko
dc.creatorRossi, Liane Marcia
dc.date.accessioned2012-04-18T23:57:37Z
dc.date.accessioned2018-07-04T14:40:16Z
dc.date.available2012-04-18T23:57:37Z
dc.date.available2018-07-04T14:40:16Z
dc.date.created2012-04-18T23:57:37Z
dc.date.issued2009
dc.identifierGREEN CHEMISTRY, v.11, n.9, p.1366-1370, 2009
dc.identifier1463-9262
dc.identifierhttp://producao.usp.br/handle/BDPI/16104
dc.identifier10.1039/b902499a
dc.identifierhttp://dx.doi.org/10.1039/b902499a
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1612926
dc.description.abstractMethyl esters were prepared by the clean, one-step catalytic esterification of primary alcohols using molecular oxygen as a green oxidant and a newly developed SiO(2)-supported gold nanoparticle catalyst. The catalyst was highly active and selective in a broad range of pressure and temperature. At 3 atm O(2) and 130 degrees C benzyl alcohol was converted to methyl benzoate with 100% conversion and 100% selectivity in 4 h of reaction. This catalytic process is much ""greener"" than the conventional reaction routes because it avoids the use of stoichiometric environmentally unfriendly oxidants, usually required for alcohol oxidation, and the use of strong acids or excess of reactants or constant removal of products required to shift the equilibrium to the desired esterification product.
dc.languageeng
dc.publisherROYAL SOC CHEMISTRY
dc.relationGreen Chemistry
dc.rightsCopyright ROYAL SOC CHEMISTRY
dc.rightsclosedAccess
dc.titleClean preparation of methyl esters in one-step oxidative esterification of primary alcohols catalyzed by supported gold nanoparticles
dc.typeArtículos de revistas


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