Novel molecular building blocks based on the boradiazaindacene chromophore: applications in fluorescent metallosupramolecular coordination polymers
dc.citation.epage | 3838 | en_US |
dc.citation.issueNumber | 15 | en_US |
dc.citation.spage | 3830 | en_US |
dc.citation.volumeNumber | 15 | en_US |
dc.contributor.author | Bozdemir, Ö. A. | en_US |
dc.contributor.author | Büyükcakir, O. | en_US |
dc.contributor.author | Akkaya, E. U. | en_US |
dc.date.accessioned | 2016-02-08T10:04:41Z | |
dc.date.available | 2016-02-08T10:04:41Z | |
dc.date.issued | 2009 | en_US |
dc.department | Department of Chemistry | en_US |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | en_US |
dc.description.abstract | We designed and synthesized novel boradiazaindacene (Bodipy) derivatives that are appropriately functionalized for metal-ion-mediated supramolecular polymerization. Thus, ligands for 2-terpyridyl-, 2,6-terpyridyl-, and bipyridyl-functionalized Bodipy dyes were synthesized through Sonogashira couplings. These fluorescent building blocks are responsive to metal ions in a stoichiometry-dependent manner. Octahedral coordinating metal ions such as Zn II result in polymerization at a stoichiometry corresponding to two terpyridyl ligands to one Zn II ion. However, at increased metal ion concentrations, the dynamic equilibria are re-established in such a way that the monomeric metal complex dominates. The position of equilibria can easily be monitored by 1H NMR and fluorescence spectroscopies. As expected, although open-shell Fe II ions form similar complex structures, these cations quench the fluorescence emission of all four functionalized Bodipy ligands. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA. | en_US |
dc.identifier.doi | 10.1002/chem.200802538 | en_US |
dc.identifier.issn | 0947-6539 | |
dc.identifier.uri | http://hdl.handle.net/11693/22783 | |
dc.language.iso | English | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1002/chem.200802538 | en_US |
dc.source.title | Chemistry - A European Journal | en_US |
dc.subject | Polymerization | en_US |
dc.subject | Self-assembly | en_US |
dc.subject | Sonogashira coupling | en_US |
dc.subject | Bipyridyl | en_US |
dc.subject | Building blocks | en_US |
dc.subject | Complex structures | en_US |
dc.subject | Coordination polymers | en_US |
dc.subject | Dyes/pigments | en_US |
dc.subject | Dynamic equilibrium | en_US |
dc.subject | Fluorescence emissions | en_US |
dc.subject | Functionalized | en_US |
dc.subject | Metal ion concentrations | en_US |
dc.subject | Metallo-supramolecular | en_US |
dc.subject | Molecular building blocks | en_US |
dc.subject | Supramolecular polymerizations | en_US |
dc.subject | Chromophores | en_US |
dc.subject | Emission spectroscopy | en_US |
dc.subject | Fluorescence | en_US |
dc.subject | Ligands | en_US |
dc.subject | Metal complexes | en_US |
dc.subject | Metal ions | en_US |
dc.subject | Metals | en_US |
dc.subject | Monomers | en_US |
dc.subject | Polymers | en_US |
dc.subject | Rhenium compounds | en_US |
dc.subject | Stoichiometry | en_US |
dc.subject | Trace analysis | en_US |
dc.subject | Zinc | en_US |
dc.subject | Functional polymers | en_US |
dc.title | Novel molecular building blocks based on the boradiazaindacene chromophore: applications in fluorescent metallosupramolecular coordination polymers | en_US |
dc.type | Article | en_US |
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