Photoluminescent properties of heteroleptic cyclometalated platinum(II) complexes bearing 1,3-bis(3,4-dibutoxyphenyl)propane-1,3-dionate as an ancillary ligand

• Published in: Journal of luminescence 2010-02, Vol.130 (2), p.217-221
• Main Authors: Tsujimoto, Hidetaka, Yagi, Shigeyuki, Honda, Yuichiro, Terao, Hiroto, Maeda, Takeshi, Nakazumi, Hiroyuki, Sakurai, Yoshiaki
• Format: Article
• Language: English
• Subjects: Ancillary ligand; Atomic and molecular physics; Cyclometalated platinum(II) complex; Exact sciences and technology; Fluorescence and phosphorescence; radiationless transitions, quenching (intersystem crossing, internal conversion); Molecular properties and interactions with photons; Phosphorescence; Photoluminescence quantum efficiency; Physics
• ISSN: 0022-2313; 1872-7883
• DOI: 10.1016/j.jlumin.2009.08.006

A new series of heteroleptic cyclometalated platinum(II) complexes Pt- 1a– f was synthesized, employing 2-arylpyridine (or 1-arylisoquinoline) ( H C ∧ N - 1) and 1,3-bis(3,4-dibutoxyphenyl)propane-1,3-dione ( H O ∧ O - 1) for cyclometalation and as ancillary ligands, respectively, and photoluminescent properties were investigated. Focusing on red-shifted phosphorescence, C ∧ N ligands containing π-extended aromatics and electron-rich heterocycles were examined. All obtained complexes exhibited photoluminescence at ambient temperature, and the emission maxima ranged from green ( λ PL=518 nm) to far red ( λ PL=708 nm). The large Stokes shifts of more than 100 nm and sub-microsecond or microsecond emission lifetimes revealed that these complexes are phosphorescent emissive. The quantum yield of Pt- 1 ranged from 0.02 to 0.59 at ambient temperature and decreased as the emission maximum was red-shifted. In comparison with the reference platinum(II) complexes, Pt- 2 bearing an aliphatic ancillary ligand, such as 2,2,6,6-tetramethylheptane-3,5-dionate ( O ∧ O - 2), the ligand O ∧ O - 1 did not significantly affect the photoluminescence emission maxima, indicating that the energy gap between the singlet ground state and the triplet level was predominantly dependent on the C ∧ N ligand.