scispace - formally typeset
Open AccessJournal ArticleDOI

Luminescent metal complexes featuring photophysically innocent boron cluster ligands

Reads0
Chats0
TLDR
This work reports the synthesis and characterization of a series of d8 metal complexes featuring robust and photophysically innocent strong-field chelating 1,1′-bis(o-carborane) (bc) ligand frameworks.
Abstract
We report the synthesis and characterization of a series of d8 metal complexes featuring robust and photophysically innocent strong-field chelating 1,1'-bis(o-carborane) (bc) ligand frameworks. A combination of UV-Vis spectroscopy, single crystal X-ray structural analysis, and DFT calculations of these species suggest that the dianionic bc ligand does not contribute to any visible metal-to-ligand charge transfer (MLCT) transitions, yet it provides a strong ligand field in these complexes. Furthermore, a bc-based Pt(II) complex containing a 4,4'-di-tert-butyl-2,2'-bipyridine ligand (dtb-bpy) has been prepared and was found to display blue phosphorescent emission dominated by MLCT from the Pt(II) center to the dtb-bpy ligand. Importantly, the bulky three-dimensional nature of the bc ligand precludes intermolecular Pt(II)⋯Pt(II) interactions in the solid state where the resulting compounds retain their emission properties. This study opens a potentially new avenue for designing organic light-emitting diode (OLED) materials with tunable properties featuring photophysically innocent boron-rich cluster ligands.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Solid‐State Emission of the Anthracene‐o‐Carborane Dyad from the Twisted‐Intramolecular Charge Transfer in the Crystalline State

TL;DR: The emission process of the o-carborane dyad with anthracene originating from the twisted intramolecular charge transfer (TICT) state in the crystalline state is described and it is proposed that the compact sphere shape of o- carborane would allow for rotation even in the condensed state.
Journal ArticleDOI

Sustainable metal complexes for organic light-emitting diodes (OLEDs)

TL;DR: In this paper, the current status of sustainable metal complexes with a special focus on copper and zinc complexes was reviewed, and the Ligand structures and complex preparation were highlighted. And the authors also briefly address features like cooperativity, chirality, and printing.
Journal ArticleDOI

Controlled functionalization of o-carborane via transition metal catalyzed B–H activation

TL;DR: A review of recent advances in transition metal catalyzed vertex-specific BH functionalization of carbon-boron molecular clusters concludes that selection of a cage C-H bonds for functionalization is very challenging.
Journal ArticleDOI

Blue Phosphorescent Zwitterionic Iridium(III) Complexes Featuring Weakly Coordinating nido-Carborane-Based Ligands.

TL;DR: The development of a new class of phosphorescent zwitterionic bis(heteroleptic) Ir(III) compounds containing pyridyl ligands with weakly coordinating nido-carboranyl substituents is reported, suggesting that the use of a ligand framework containing aWeakly coordinating anionic component can provide a new avenue for designing efficient Ir( III)-based phosphorescent emitters.
Journal ArticleDOI

Transition Metal Catalyzed Direct Amination of the Cage B(4)-H Bond in o-Carboranes: Synthesis of Tertiary, Secondary, and Primary o-Carboranyl Amines.

TL;DR: Transition metal catalyzed regioselective amination of the cage B(4)-H bond in o-carboranes has been achieved for the first time using O-benzoyl hydroxylamines or organic azides as the amination reagents, leading to the preparation of a series of tertiary and secondary carboranyl amines.
References
More filters
Journal ArticleDOI

Ammonia as a case study for the spontaneous ionization of a simple hydrogen-bonded compound

TL;DR: Experimental evidence is presented that the threshold pressure of ~120 GPa induces in molecular ammonia the process of autoionization to yet experimentally unknown ionic compound--ammonium amide, opening new possibilities for studying molecular interactions in hydrogen-bonded systems.
Journal ArticleDOI

Chemical Redox Agents for Organometallic Chemistry

TL;DR: 1. Advantages and disadvantages of Chemical Redox Agents, 2. Reversible vs Irreversible ET Reagents, 3. Categorization of Reagent Strength.
Journal ArticleDOI

Synthesis and characterization of phosphorescent cyclometalated platinum complexes.

TL;DR: The synthesis, electrochemistry, and photophysics of a series of square planar Pt(II) complexes are reported, with well-resolved vibronic fine structure observed in all of the emission spectra.
Journal ArticleDOI

Transition-metal phosphors with cyclometalating ligands: fundamentals and applications

TL;DR: 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, are reviewed.
Related Papers (5)