Synthesis and characterization of phosphorescent platinum and iridium complexes with cyclometalated corannulene

被引:11
作者
Facendola, John W. [1 ]
Seifrid, Martin [1 ]
Siegel, Jay [2 ]
Djurovich, Peter I. [1 ]
Thompson, Mark E. [1 ]
机构
[1] Univ So Calif, Dept Chem, Los Angeles, CA 90089 USA
[2] Tianjin Univ, Sch Pharmaceut Sci & Technol, Tianjin 300072, Peoples R China
基金
美国国家科学基金会;
关键词
BOWL-INVERSION BARRIER; AROMATIC-HYDROCARBONS; FULLERENE CHEMISTRY; IR(III) COMPLEXES; PHOTOPHYSICAL PROPERTIES; CHARGE-TRANSPORT; COORDINATION; DERIVATIVES; LIGANDS; BLUE;
D O I
10.1039/c4dt03541k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Synthesis, structural and characterization data are provided for Pt(II) and Ir(III) complexes cyclometalated with 2-(corannulene)pyridine (corpy), (corpy)Pt(dpm) and (corpy)Ir(ppz)2 (dpm = dipivaloylmethanato, ppz = 1-phenylpyrazolyl). A third compound, (phenpy)Ir(ppz)(2) (phenpy = 2-(5-phenanthryl)-pyridyl), was also prepared to mimic the steric bulk of (corpy)Ir(ppz)(2). X-ray analysis reveals bowl depths of 0.895 angstrom for (corpy)Pt(dpm) and 0.837 angstrom in (corpy)Ir(ppz)(2). Neither complex displayed bowl-to-bowl stacking in the crystal lattice. A fluxional process for (corpy)Ir(ppz)(2) attributed to bowl inversion of corrannulene is observed in solution with a barrier (Delta G(double dagger) = 13 kcal mol(-1)) and rate (k = 2.5 x 10(3) s(-1)) as determined using variable temperature H-1 NMR spectroscopy. All of the complexes display red phosphorescence at room temperature with quantum yields of 0.05 in solution and 0.2 in polymethyl methacrylate (PMMA).
引用
收藏
页码:8456 / 8466
页数:11
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