Transition-metal phosphors with cyclometalating ligands: fundamentals and applications
Фосфоры на переходных металлах с цикломулирующими лигандами: основы и приложения
2009-12-07
SCID: 54.1/7cqdfgaw
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Ir(III) complexesN-heterocyclic carbene (NHC)cyclometalating ligandsorganic light emitting diodes (OLEDs)transition-metal phosphors
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Abstract (AI)
One goal of this critical review is to provide advanced methodologies for systematic preparation of transition-metal based phosphors that show latent applications in the field of organic light emitting diodes (OLEDs). We are therefore reviewing various types of cyclometalating chelates for which the favorable metal-chelate bonding interaction, on the one hand, makes the resulting phosphorescent complexes highly emissive in both fluid and solid states at room temperature. On the other hand, fine adjustment of ligand-centered pi-pi* electronic transitions allows tuning of emission wavelength across the whole visible spectrum. The cyclometalating chelates are then classified according to types of cyclometalating groups, i.e. either aromatic C-H or azolic N-H fragment, and the adjacent donor fragment involved in the formation of metallacycles; the latter is an N-containing heterocycle, N-heterocyclic (NHC) carbene fragment or even diphenylphosphino group. These cyclometalating ligands are capable to react with heavy transition-metal elements, namely: Ru(II), Os(II), Ir(III) and Pt(II), to afford a variety of highly emissive phosphors, for which the photophysical properties as a function of chelate or metal characteristics are systematically discussed. Using Ir(III) complexes as examples, the C--N chelates possessing both C-H site and N-heterocyclic donor group are essential for obtaining phosphors with emission ranging from sky-blue to saturated red, while the N--N chelates such as 2-pyridyl-C-linked azolates are found useful for serving as true-blue chromophores due to their increased ligand-centered pi-pi* energy gap. Lastly, the remaining NHC carbene and benzyl phosphine chelates are highly desirable to serve as ancillary chelates in localizing the electronic transition between the metal and remaining lower energy chromophoric chelates. As for the potential opto-electronic applications, many of them exhibit remarkable performance data, which are convincing to pave a broad avenue for further development of all types of phosphorescent displays and illumination devices (94 references).
Key Findings
1
Cyclometalating chelates form strong metal-chelate bonds producing highly emissive transition-metal phosphorescent complexes in fluid and solid states at room temperature.
2
Cyclometalating ligands are classified by cyclometalating group (aromatic C-H or azolic N-H) and adjacent donor fragment (N-heterocycle, NHC carbene, or diphenylphosphino), which systematically affects photophysical properties.
3
Ir(III) C–N chelates (C-H site plus N-heterocyclic donor) yield emissions from sky-blue to saturated red, while N–N chelates like 2-pyridyl-C-linked azolates produce true-blue chromophores due to larger ligand-centered pi-pi* gaps.
4
NHC carbene and benzyl phosphine chelates are effective ancillary ligands that localize electronic transitions between the metal and lower-energy chromophoric chelates, aiding device design for OLEDs and displays.
5
Tuning ligand-centered pi-pi* transitions in cyclometalating ligands enables emission wavelength control across the entire visible spectrum.
Research Object
Transition-metal phosphorescent complexes with cyclometalating ligands (e.g., Ru(II), Os(II), Ir(III), Pt(II) complexes)
Research Subject
Photophysical properties and emission tuning (wavelength across visible spectrum, ligand-centered pi–pi* transitions, effect of chelate type and metal) of these cyclometalated phosphors and their suitability for OLED/optoelectronic applications
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2009-12-07
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