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      Cation-controlled luminescence behavior of anionic cyclometalated platinum(II) complexes

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      Coordination Chemistry Reviews

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          VESTA 3for three-dimensional visualization of crystal, volumetric and morphology data

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            The triplet state of organo-transition metal compounds. Triplet harvesting and singlet harvesting for efficient OLEDs

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              Transition-metal phosphors with cyclometalating ligands: fundamentals and applications.

              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).
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                Author and article information

                Journal
                Coordination Chemistry Reviews
                Coordination Chemistry Reviews
                00108545
                April 2020
                April 2020
                : 408
                : 213194
                Article
                10.1016/j.ccr.2020.213194
                950a3503-41d1-4257-9779-f31caa48bba9
                © 2020

                https://www.elsevier.com/tdm/userlicense/1.0/

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