Various Structural Design Modifications : para-Substituted Diphenylphosphinopyridine Bridged Cu(I) Complexes in Organic Light-Emitting Diodes

The well-known system of dinuclear Cu(I) complexes bridged by 2-(diphenylphosphino)pyridine (PyrPhos) derivatives Cu2X2L3 and Cu2X2LP2 (L = bridging ligand, P = ancillary ligand) goes along with endless variation options for tunability. In this work, the influence of substituents and modifications on the phosphine moiety of the NP-bridging ligand was investigated. In previous studies, the location of the lowest unoccupied molecular orbital (LUMO) of the copper complexes of the PyrPhos family was found to be located on the NP-bridging ligand and enabled color tuning in the whole visible spectrum. A multitude of dinuclear Cu(I) complexes based on the triple methylated 2- (bis (4-methylphenyl)phosphino)-4-methylpyridine (Cu-1b-H, Cu-1b-MeO, and Cu-1b-F) up to complexes bearing 2-(bis(4-fluorophenyl)phosphino)pyridine (Cu-6a-H) with electron-withdrawing fluorine atoms over many other variations on the NP-bridging ligands were synthesized. Almost all copper complexes were confirmed via single crystal X-ray diffraction analysis. Besides theoretical TDDFT-studies of the electronic properties and photophysical measurements, the majority of the phosphinomodified Cu(I) complexes was tested in solution-processed organic light-emitting diodes (OLEDs) with different heterostructure variations. The best results of the OLED devices were obtained with copper emitter Cu-lb-H in a stack architecture of ITO/PEDOT-PSS (50 nm)/poly-TPD (15 nm)/20 wt % Cu(I) emitter:CBP:TcTA(7:3) (45 nm)/TPBi (30 nm)/LiF(1 nm)/Al (>100 nm) with a high brightness of 5900 Cd/m(2) and a good current efficiency of 3.79 Cd/A.Peer reviewe

Remarkable high efficiency of red emitters using Eu(III) ternary complexes

We have synthesized Eu(iii) ternary complexes possessing record photoluminescence yields up to 90%. This high luminescence performance resulted from the absence of quenching moieties in the Eu coordination environment and an efficient energy transfer between ligands, combined with a particular symmetry of the coordination environment

Synthesis and chemical transformations of diazolyl alpha,alpha-difluoroacetates

Optimized protocols for the synthesis of diazolyl alpha,alpha-difluoroacetates via deoxofluorination of the corresponding glyoxylates with Morph-DAST are described. The method allowed the preparation of the title fluoridated building blocks in 73-96 % yield on up to 15 g scale. Utility of the hetaryl alpha,alpha-difluoroacetates was demonstrated by the synthesis of advanced building blocks for medicinal chemistry, i.e. carboxylic acids, amides, nitriles, and alcohols

Novel D-A-D Fluorescent Dyes Based on 9-(p-Tolyl)-2,3,4,4a,9,9a-hexahydro-1H-carbazole as a Donor Unit for Solution-Processed Organic Light-Emitting-Diodes

New fluorescent D-A-D dyes containing 9-(p-tolyl)-2,3,4,4a,9,9a-hexahydro-1H-carbazole as a donor unit and 2,1,3-benzochalcogenadiazoles as an electron-withdrawing group were synthesized. The photoluminescent and electroluminescent properties of novel dyes for fluorescent OLED application were investigated. It was demonstrated that the replacement of lightweight heteroatoms by heavier ones enables the fine tuning of the maximum emission without significantly reducing the luminescence quantum yield. The maximum quantum yield value of 62.6% for derivatives based on 2,1,3-benzoxadiazole (1a) in cyclohexane was achieved. Two devices with the architecture of glass/ITO/PEDOT-PSS/poly-TPD/EML/TPBi/LiF/Al (EML = emitting layer) were fabricated to check the suitability of the synthesized compounds as a single active emission layer in OLED. These OLEDs exhibited clear red electroluminescence of the dyes with the maximum current efficiency of 0.85 Cd/A

Lanthanide 9-anthracenate: solution processable emitters for efficient purely NIR emitting host-free OLEDs

Searching for new NIR emitting materials, lanthanide 9-anthracenates Ln(ant)3 were synthesized and thoroughly characterized. Ytterbium 9-anthracenate Yb(ant)3, that demonstrated the highest NIR luminescence efficiency, was successfully used as an emission layer of a host-free OLED and its electroluminescence quantum efficiency, corresponding to the sole band at 1000 nm, reached 0.21%. This performance could be achieved due to the high quantum yield of Yb(ant)3, which reached 1.5% and was increased up to 2.5% by partial Yb3+ substitution with Lu3+, as well as its high electron mobility due to the extended stacking in its crystal structure. The first gadolinium-based PHOLED was prepared based on Gd(ant)3

OLED thin film fabrication from poorly soluble terbium o-phenoxybenzoate through soluble mixed-ligand complexes

Features and advantages of the approach of the luminescent thin film deposition of non-volatile and non-soluble lanthanide aromatic carboxylates were exemplified by thin film deposition of terbium o-phenoxybenzoate Tb(pobz)3(H2O)2 (I) with quantum yield measured to be 96%. This approach is based on the formation and decomposition of mixed-ligand complexes, and thus mixed-ligand complex Tb(pobz)3(MG)(H2O)2 (II) (MG - monoglyme) was synthesized, characterized and used as a precursor for I thin films. Electroluminescent (EL) properties of high quality thin films of I and those with suitable host material were studied in a series of OLED devices

Thermodynamically Stable Dispersions of Quantum Dots in a Nematic Liquid Crystal

Using transmittance electron microscopy, fluorescence and polarizing optical microscopy, optical spectroscopy, and fluorescent correlation spectroscopy, it was shown that CdSe/ZnS quantum dots coated with a specifically designed surfactant were readily dispersed in nematic liquid crystal (LC) to form stable colloids. The mixture of an alkyl phosphonate and a dendritic surfactant, where the constituent molecules contain promesogenic units, enabled the formation of thermodynamically stable colloids that were stable for at least 1 year. Stable colloids are formed due to minimization of the distortion of the LC ordering around the quantum dots