The last decade has seen a surge of interest in the emissive behaviour of copper(i) coordination compounds, both neutral compounds that may have applications in organic light-emitting doides (OLEDs) and copper-based ionic transition metal complexes (Cu-iTMCs) with potential use in light-emitting electrochemical cells (LECs). One of the most exciting features of copper(i) coordination compounds is their possibility to exhibit thermally activated delayed fluorescence (TADF) in which the energy separation of the excited singlet (S1) and excited triplet (T1) states is very small, permitting intersystem crossing (ISC) and reverse intersystem crossing (RISC) to occur at room temperature without the requirement for the large spin-orbit coupling inferred by the presence of a heavy metal such as iridium. In this review, we focus mainly in Cu-iTMCs, and illustrate how the field of luminescent compounds and those exhibiting TADF has developed. Copper(i) coordination compounds that class as Cu-iTMCs include those containing four-coordinate [Cu(P^P)(N^N)]+ (P^P = large-bite angle bisphosphane, and N^N is typically a diimine), [Cu(P)2(N^N)]+ (P = monodentate phosphane ligand), [Cu(P)(tripodal-N3)]+, [Cu(P)(N^N)(N)]+ (N = monodentate N-donor ligand), [Cu(P^P)(N^S)]+ (N^S = chelating N,S-donor ligand), [Cu(P^P)(P^S)]+ (P^S = chelating P,S-donor ligand), [Cu(P^P)(NHC)]+ (NHC = N-heterocyclic carbene) coordination domains, dinuclear complexes with P^P and N^N ligands, three-coordinate [Cu(N^N)(NHC)]+ and two-coordinate [Cu(N)(NHC)]+ complexes. We pay particular attention to solid-state structural features, e.g. π-stacking interactions and other inter-ligand interactions, which may impact on photoluminescence quantum yields. Where emissive Cu-iTMCs have been tested in LECs, we detail the device architectures, and this emphasizes differences which make it difficult to compare LEC performances from different investigations. 

/pdf/tadf-enabling-luminescent-copper-scp-i-scp-coordination-we040p8v.pdf

TADF: Enabling luminescent copper(<scp>i</scp>) coordination compounds for light-emitting electrochemical cells

Non-covalent intramolecular interactions through ligand-design promoting efficient photoluminescence from transition metal complexes

The synthesis and photophysical study of two dinuclear copper(I) complexes bearing a 2-(1H-imidazol-2-yl)pyrimidine bridging ligand are described. The tetrahedral coordination sphere of each copper center is completed through the use of a bulky bis(phosphine) ligand, either DPEphos or Xantphos. Temperature-dependent photophysical studies demonstrated emission through a combination of phosphorescence and thermally activated delayed fluorescence for both complexes, and an intense emission (ΦPL = 46%) was observed for a crystalline sample of one of the complexes reported. The photophysics of these two complexes is very sensitive to the environment. Two pseudopolymorphs of one of the dinuclear complexes were isolated, with distinct photophysics. The emission color of the crystals can be changed by grinding, and the differences in their photophysics before and after grinding are discussed.

/pdf/luminescent-dinuclear-copper-i-complexes-bearing-an-302yw7lvks.pdf

Luminescent Dinuclear Copper(I) Complexes Bearing an Imidazolylpyrimidine Bridging Ligand.

Structural characterization, electronic and luminescent properties of copper(I) complexes with different temperatures and their application to light-emitting diodes

Smart luminescent materials, which can respond to the changing of external environment (light, electricity, force, temperature, etc.), have always been one of the research hotspots. Mechanochromism refers to the materials whose emission color or intensity can be altered under the stimulation of external mechanical force. This kind of smart materials have been widely used in data storage, information encryption and sensors due to its simple operation, obvious and rapid response. The introduction of metal atoms in metal-organic compounds brings about fascinating metalophilic interactions and results in more interesting and surprising mechanochromic behaviors. In this mini-review, recent advances in mechanochromism of metal-organic compounds, including mono-, di-, multinuclear metal-organic complexes and metallic clusters are summarized. Varies mechanisms are discussed and some design strategies for metal-organic compounds with mechanochromism are also presented. 

Recent Advances in Mechanochromism of Metal-Organic Compounds

A series of easily accessible linear N-heterocyclic carbene (NHC) copper(I) complexes, bearing pyridine (py) and its derivatives as chromophore ligands, are barely emissive in the single-crystallin...

Correction to "Cu-F Interactions between Cationic Linear N-Heterocyclic Carbene Copper(I) Pyridine Complexes and Their Counterions Greatly Enhance Blue Luminescence Efficiency".

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Correction to "Cu-F Interactions between Cationic Linear N-Heterocyclic Carbene Copper(I) Pyridine Complexes and Their Counterions Greatly Enhance Blue Luminescence Efficiency".