Cubic nonlinear optical properties of new zinc tetraphenyl porphyrins peripherally functionalized with electron-rich Ru(II) alkynyl substituents

dc.contributor.authorDrouet, Samuel
dc.contributor.authorMerhi, Areej
dc.contributor.authorYao, Dandan
dc.contributor.authorCifuentes, Marie
dc.contributor.authorWielgus, Malgorzata
dc.contributor.authorOlesiak-Banska, Joanna
dc.contributor.authorMatczyszyn, Katarzyna
dc.contributor.authorSamoc, Marek
dc.contributor.authorPaul, Frederic
dc.contributor.authorPaul-Roth, Christine
dc.contributor.authorHumphrey, Mark
dc.date.accessioned2016-02-24T22:40:43Z
dc.date.issued2012
dc.date.updated2016-02-24T08:52:14Z
dc.description.abstractWe report the synthesis and characterization of new organometallic assemblies consisting of a central Zn(II) tetraphenylporphyrin (ZnTPP) core surrounded by four Ru(II) alkynyl complexes (trans-Ru(dppe)2R) appended at the para phenyl positions and acting as peripheral donor groups. The synthesis of the tetra-chlorido derivative 2 (R=Cl) is reported first, followed by that of three extended homologues (3-X) obtained from this building block by substitution of the chlorido ligands by functionalized arylacetylenes (R=CC(4-C6H4X); X=NO2, H, OMe). Measurement of the nonlinear absorption properties of the pentametallic derivatives 3-X reveals that these extended π-networks incorporating polarizable organometallic units behave as good two-photon absorbers in the visible and near-IR range.
dc.identifier.issn0040-4020
dc.identifier.urihttp://hdl.handle.net/1885/98419
dc.publisherElsevier
dc.sourceTetrahedron
dc.subjectKeywords: acetylene derivative; alkynyl group; organometallic compound; polycyclic aromatic hydrocarbon derivative; ruthenium derivative; tetraphenylporphyrin derivative; zinc derivative; article; chemical reaction; complex formation; fluorescence microscopy; near Acetylide complex; Nonlinear optics; Organometallics; Pi-conjugation; Porphyrin
dc.titleCubic nonlinear optical properties of new zinc tetraphenyl porphyrins peripherally functionalized with electron-rich Ru(II) alkynyl substituents
dc.typeJournal article
local.bibliographicCitation.issue50
local.bibliographicCitation.lastpage10359
local.bibliographicCitation.startpage10351
local.contributor.affiliationDrouet, Samuel, Institut de Sciences Chimiques de Rennes
local.contributor.affiliationMerhi, Areej, Universite Europeenne de Bretagne
local.contributor.affiliationYao, Dandan, Universite Europeenne de Bretagne
local.contributor.affiliationCifuentes, Marie, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHumphrey, Mark, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationWielgus, Malgorzata, Wroclaw University of Technology
local.contributor.affiliationOlesiak-Banska, Joanna, Wroclaw University of Technology
local.contributor.affiliationMatczyszyn, Katarzyna, Wroclaw UniVersity of Technology
local.contributor.affiliationSamoc, Marek, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationPaul, Frederic, Universite de Rennes
local.contributor.affiliationPaul-Roth, Christine, Universite Rennes 1
local.contributor.authoruidCifuentes, Marie, u9410034
local.contributor.authoruidHumphrey, Mark, u9400918
local.contributor.authoruidSamoc, Marek, u9115357
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor039904 - Organometallic Chemistry
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.ariespublicationf5625xPUB1967
local.identifier.citationvolume68
local.identifier.doi10.1016/j.tet.2012.09.108
local.identifier.scopusID2-s2.0-84869090821
local.identifier.thomsonID000311135700012
local.type.statusPublished Version

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