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Luminescent Cycloplatinated Complexes Containing Poly(pyrazolyl)-borate and -methane Ligands.
- Source :
-
Organometallics . Nov2011, Vol. 30 Issue 21, p5776-5792. 17p. - Publication Year :
- 2011
-
Abstract
- Cycloplatinated neutral [Pt(Câ§N){H2B(pz)2}] (1â3) [Câ§N = benzoquinolate (bzq), 2-phenylpyridinate (ppy), and 2-phenylquinolate (pq)] and [Pt(pq){HB(pz)3}] 10and cationic [Pt(Câ§N){H2C(pz)2}](4â6) and [Pt(Câ§N){HC(pz)3}](7â9) complexes were synthesized by the reaction of the corresponding precursors [Pt(Câ§N)(μ-Cl)]2with the adequate poly(pyrazolyl)-borate or -methane ligand. However, the reactions of [Pt(Câ§N)(μ-Cl)]2(Câ§N = bzq, ppy) with [HB(pz)3]âevolve with BâN bond cleavage, yielding the binuclear systems [Pt(Câ§N)(μ-pz)]2as a mixture of cis and trans isomers. Complexes were characterized in solution by multinuclear and multidimensional NMR spectroscopy. The solid-state structures of 1, 3, 6, 7â9, and [Pt(bzq)(μ-pz)]2were confirmed by X-ray single-crystal studies. The absorption, emission, and electrochemical properties of these complexes are mainly dominated by the nature of the cyclometalated ligand and the charge of the complex. On the basis of TD-DFT calculations (1, 7â9), the lowest-energy absorption for neutral 1has been ascribed to a mixed 1ILCT/1MLCT transition, whereas for the cationic 7â9, it is mainly attributed to 1ILCT combined with some CT to both ligands in 9(1MLCT/MLâ²CT 9) or to the HC(pz)3in 7and 8(1MLâ²CT). These compounds are emissive in all media (except 4and 10in the solid state at 298 K). In the solid state at 298 K and at 77 K, these complexes display intense phosphorescence, which is typical of monomers. In deoxygenated CH3CN solutions at 298 K, phosphorescence is accompanied by higher-energy fluorescence in complexes 1, 4, and 8, which disappears at concentrated solutions and at 77 K. Complex 7displays a special behavior, observing fluorescence and/or excimer fluorescence only at 298 K and excimeric emission (diluted glasses) and emission from aggregates in concentrated glasses. TD-DFT of the lowest-lying excited states responsible for the phosphorescence of 1and 7â9reveals a 3ILCT origin with a mixed 3MLCT character for 1and, in the case of the cationic 7â9, a 3ILCT transition mixed with 3MLâ²CT (especially in 8) and with some 3MLCT in 9. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 02767333
- Volume :
- 30
- Issue :
- 21
- Database :
- Academic Search Index
- Journal :
- Organometallics
- Publication Type :
- Academic Journal
- Accession number :
- 67086057
- Full Text :
- https://doi.org/10.1021/om200624v