Direction of copper phthalocyanine crystallization using in situ generated tethered phthalocyanines

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dc.contributor.authorMoynihan, Humphrey A.
dc.contributor.authorClaudon, Geraldine
dc.contributor.funderEnterprise Irelanden
dc.contributor.funderEuropean Commissionen
dc.date.accessioned2014-07-21T13:27:58Z
dc.date.available2014-07-21T13:27:58Z
dc.date.issued2010-05
dc.date.updated2014-07-08T15:12:32Z
dc.description.abstractCopper phthalocyanine in the metastable α crystal polymorph can be obtained directly from phthalonitrile or from phthalodiimide, which would normally give the more stable β crystal form, by the inclusion of 3% or greater of the sulfide 2 or the diimide 3. The resulting α form material does not revert to the β form upon treatment in boiling xylene, unlike conventionally prepared α copper phthalocyanine.en
dc.description.sponsorshipEnterprise Ireland (PC/2004/0443 and PC/2007/0129); European Commission (FP6 Marie Curie Fellowships (MTKD-CT-2005-029896))en
dc.description.statusPeer revieweden
dc.description.versionAccepted Versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationMOYNIHAN, H. A. & CLAUDON, G. 2010. Direction of copper phthalocyanine crystallization using in situ generated tethered phthalocyanines. CrystEngComm, 12 (10), 2695-2696. DOI: http://dx.doi.org/10.1039/C004048Gen
dc.identifier.doi10.1039/c004048g
dc.identifier.endpage2696en
dc.identifier.issn1466-8033
dc.identifier.issued10en
dc.identifier.journaltitleCrystEngCommen
dc.identifier.startpage2695en
dc.identifier.urihttps://hdl.handle.net/10468/1593
dc.identifier.volume12en
dc.language.isoenen
dc.publisherThe Royal Society of Chemistryen
dc.rights© The Royal Society of Chemistry 2010en
dc.subjectCopper phthalocyanineen
dc.subjectOrganic pigmentsen
dc.titleDirection of copper phthalocyanine crystallization using in situ generated tethered phthalocyaninesen
dc.typeArticle (peer-reviewed)en
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