Incorporation of a Fluorine Atom in a Bridging Ligand of Half-Lantern Pt Complexes Provides up to 10-Fold Enhancement of Electroluminescence Brightness.

The binuclear half-lantern platinum(II) complexes [Pt(pbt)(μ-SN)] (pbtH = 2-phenylbenzothiazole, SN = benzo[]thiazole-2-thiolate , 6-fluorobenzo[]thiazole-2-thiolate , 6-chlorobenzo[]thiazole-2-thiolate , 6-bromobenzo[]thiazole-2-thiolate , and 6-iodobenzo[]thiazole-2-thiolate ) were synthesized by the treatment of the in situ formed [Pt(pbt)(NCMe)]NO complex and appropriate benzo[]thiazole-2-thiole in the presence of BuOK; yield: 51-84%. Complexes - exhibit intense red photoluminescence originated from MMLCT state reaching 22% room temperature quantum yields in a CHCl solution. All complexes display excited-state decay kinetics both in solution and in the solid state; the kinetics was adequately modeled by single exponentials.

Fast Recombination of Charge-Transfer State in Organic Photovoltaic Composite of P3HT and Semiconducting Carbon Nanotubes Is the Reason for Its Poor Photovoltaic Performance.

Although the photovoltaic performance of the composite of poly-3-hexylthiophene (P3HT) with semiconducting single-walled carbon nanotubes (s-SWCNT) is promising, the short-circuit current density is much lower than that for typical polymer/fullerene composites. Out-of-phase electron spin echo (ESE) technique with laser excitation of the P3HT/s-SWCNT composite was used to clarify the origin of the poor photogeneration of free charges. The appearance of out-of-phase ESE signal is a solid proof that the charge-transfer state of P3HT/s-SWCNT is formed upon photoexcitation and the electron spins of P3HT and s-SWCNT are correlated.

Spectral-Luminescent and Electroluminescent Properties of Charge-transfer Systems Based On Electron-donating Diphenylamine Derivatives and Acceptors of Dibenzothiophene Sulfone and Phenanthridine.

Spectral characteristics and luminescence under the photo- and electro-excitation of substituted dibenzthiophene sulfone and phenanthridine were studied in this paper. Diphenylamines are substituents introduced in the 2nd and 7th positions (linear configuration) or the 3rd and 6th positions (angular configuration) of dibenzthiophene sulfone or phenanthridine. All molecules show delayed fluorescence, both in solutions and films produced by thermal vacuum deposition.

Luminescent Properties of Zn and Mg Complexes on N-(2-Carboxyphenyl)salicylidenimine Basis.

New zinc and magnesium complexes of N-(2-carboxyphenyl)salicylidenimine) were synthesized and structurally characterized by elemental analysis, FT-IR, and X-ray single-crystal analysis. These complexes exhibit tuneable luminescence in the solid state from blue to green by varying by metal ion and composition. Moreover, the quantum yields range from 0.

Experimental and theoretical study of photo- and electroluminescence of divinyldiphenyl and divinylphenanthrene derivatives.

Electronic absorption and luminescence spectra of four new compounds of divinyldiphenyl and divinylphenanthrene derivatives are investigated experimentally in tetrahydrofuran solutions and thin films obtained by thermal vacuum deposition and by spin coating of these substances embedded into polyvinylcarbazole matrix. Molecular geometry optimizations and electronic spectra have been calculated in the framework of XMC-QDPT2/6-31G (d, p) and TDDFT/B3LYP/6-31G (d, p) levels of theory. We have fabricated and studied OLED devices with the structure ITO/PEDOT:PSS/NPD/L/Ca/Al and ITO/PEDOT:PSS/PVK+L/Ca, where L is the luminophore.