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filingDate 2011-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7c8f67a387432e9a226c87eb02a35620
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_951479ed628e31a110781c88f4218fb6
publicationDate 2014-05-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-8735522-B2
titleOfInvention Gold-polymer nanostructure-immobilized scandium catalyst and its use
abstract The present invention provides a Scandium catalyst that can be used in water or water-soluble organic solvent with no leaching of Scandium. Provided is a gold-polymer nanostructure-immobilized Scandium catalyst, which is formed by preparing, in liquid phase, a mixture comprising gold clusters with from 1 to 50 nm of diameter, disulfide monomer, sulfonic acid salt of disulfide and Lewis acid metal compound represented by ScY 3 , wherein Y is OSO 2 CF 3 etc., and polymerizing the mixture in the presence of a radical polymerization initiator, wherein the disulfide monomer is represented by the formula below:n nCH 2 ═CH—R 1 —S—S—R 1 —CH═CH 2 n nwherein R 1 represents a divalent hydrocarbon, which may contain an ether bond, and the sulfonic acid salt of disulfide is represented by the formula below:n nMO 3 S—R 2 —S—S—R 2 —SO 3 Mn nwherein R 2 represents a divalent hydrocarbon, which may contain an ether bond, and M represents an alkali metal. This catalyst is useful as a catalyst for aldol reactions, cyanolation reactions, allylation reactions, Michael reactions, Mannich reactions, Diels Alder reactions and Friedel Crafts reactions in water or water-soluble organic solvent.
priorityDate 2010-03-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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