Methylated Re( I ) tetrazolato complexes: photophysical properties and Light Emitting Devices (Articolo in rivista)

Type
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  • Methylated Re( I ) tetrazolato complexes: photophysical properties and Light Emitting Devices (Articolo in rivista) (literal)
Anno
  • 2015-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1039/c4dt03228d (literal)
Alternative label
  • Melissa V. Werrett,ab Gregory S. Huff,cd Sara Muzzioli,b Valentina Fiorini,b Stefano Zacchini,b Brian W. Skelton,e Antonio Maggiore,f Joanna M. Malicka,f Massimo Cocchi,fg Keith C. Gordon,cd Stefano Stagni,* and Massimiliano Massi,a (2015)
    Methylated Re( I ) tetrazolato complexes: photophysical properties and Light Emitting Devices
    in Dalton transactions (2003. Online)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Melissa V. Werrett,ab Gregory S. Huff,cd Sara Muzzioli,b Valentina Fiorini,b Stefano Zacchini,b Brian W. Skelton,e Antonio Maggiore,f Joanna M. Malicka,f Massimo Cocchi,fg Keith C. Gordon,cd Stefano Stagni,* and Massimiliano Massi,a (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
  • HOT articles http://blogs.rsc.org/dt/category/hot-articles/ (literal)
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Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • a Department of Chemistry, Curtin University, Kent Street, Bentley WA 6102, Australia b Department of Industrial Chemistry \"Toso Montanari\", University of Bologna, viale del Risorgimento 4, 40126 Bologna, Italy E-mail: stefano.stagni@unibo.it c Department of Chemistry, University of Otago, Union Place, Dunedin, New Zealand d MacDiarmid Institute for Advanced Materials and Nanotechnology, New Zealand e Centre for Microscopy, Characterisation and Analysis, University of Western Australia, Crawley 6009 WA, Australia f Consorzio MIST E-R Via P. Gobetti 101, 40129 Bologna, Italy g Institute for Organic Synthesis and Photoreactivity, CNR, via Gobetti 101, 40129 Bologna, Italy (literal)
Titolo
  • Methylated Re( I ) tetrazolato complexes: photophysical properties and Light Emitting Devices (literal)
Abstract
  • The irreversible reaction of methyl triflate with neutral Re(I) tetrazolato complexes of the type fac-[Re(diim)(CO)3(L)], where diim is either 1,10-phenanthroline or 2,2?-bipyridine and L is a para substituted 5-aryltetrazolate, yielded the corresponding cationic methylated complexes. While methylation occurred regioselectively at the N4 position of the tetrazole ring, the cationic complexes were found to exist in solution as equilibrating mixtures of linkage isomers, where the Re(I) centre was bound to either the N1 or N2 atom of the tetrazole ring. The existence of these isomers was highlighted both by NMR and X-ray crystallography studies. On the other hand, the two isomers appeared indistinguishable by IR, UV-Vis and luminescence spectroscopy. The prepared cationic complexes are all brightly phosphorescent in fluid and rigid solutions, with emission originating from triplet metal-to-ligand charge transfer excited states. Compared to their neutral precursors, which emit from admixtures of triplet metal-to-ligand and ligand-to-ligand charge transfer states, the methylated complexes exhibit blue-shifted emission characterised by elongated excited state lifetimes and increased quantum yields. The nature of the excited states for both the neutral and the methylated complexes was probed by resonance Raman spectroscopy and with the aid of time-dependent density functional theory calculations. Lastly, both the neutral and the methylated species were used as emitting phosphors in the fabrication of Organic Light Emitting Diodes and Light Emitting Electrochemical Cells. (literal)
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