Utilize este identificador para referenciar este registo: https://hdl.handle.net/1822/5259

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Campo DCValorIdioma
dc.contributor.authorGupta, Sanjay-
dc.contributor.authorSivasubramanian, Aravind-
dc.contributor.authorRodrigues, Lígia M.-
dc.contributor.authorEsteves, Ana Paula-
dc.contributor.authorHrdina, Radim-
dc.contributor.authorCampos, Ana M. F. Oliveira-
dc.date.accessioned2006-07-18T15:32:33Z-
dc.date.available2006-07-18T15:32:33Z-
dc.date.issued2007-
dc.identifier.issn0143-7208por
dc.identifier.urihttps://hdl.handle.net/1822/5259-
dc.description.abstractEight dyes were prepared by diazotisation of substituted amino-cyano pyrazoles and coupling to anilines or 2-naphthol. The dyes were fully characterised by spectroscopic techniques. The cyano group of the pyrazoles was found to be susceptible to hydrolysis during preparation.eng
dc.description.sponsorshipFundação para a Ciência e Tecnologia - SFRH/BPD/20816/2004.eng
dc.description.sponsorshipFEDER.eng
dc.description.sponsorshipMinistry of Education, Youth and Sports of the Czech Republic - Project CZ 351002.eng
dc.language.isoengeng
dc.publisherElsevier Science Ltdpor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBPD%2F20816%2F2004/PT-
dc.rightsopenAccesseng
dc.subjectCyanopyrazoleeng
dc.subjectAzo dyeseng
dc.subjectDiazotisationeng
dc.titleSynthesis of dyes derived from 1-aryl-5-amino-4-cyanopyrazoleseng
dc.typearticlepor
dc.peerreviewedyeseng
dc.relation.publisherversionwww.elsevier.comeng
dc.relation.publisherversionhttp://www.sciencedirect.com/science?_ob= ArticleListURL&_method=list&_ArticleListID= 449960047&_sort=d&view=c&_acct=C000057396 &_version=1&_urlVersion=0&_userid=2459786&md 5=fd261ef7e7088994572d12834b2c2c57-
sdum.publicationstatusin publicationeng
oaire.citationStartPage82por
oaire.citationEndPage87por
oaire.citationIssue1por
oaire.citationVolume75por
dc.identifier.doi10.1016/j.dyepig.2006.04.016por
dc.subject.wosScience & Technologypor
sdum.journalDyes and Pigmentspor
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