Photoluminescent chain-of-dimer anion in a novel hybrid halometallate (CHN){SbBr}: atypical behavior in one-dimensional anionic systems.

In pursuit of identifying less toxic hybrid compounds suitable for optoelectronic applications, we synthesized a novel homopiperazinium bromoantimonate(III), (CHN){SbBr}. It readily crystallized from an aqueous hydrobromic acid solution and was found to be stable both in air and upon heating up to 175 °C. The crystal structure of the new bromoantimonate(III) consisted of {SbBr} zigzag chains, which were composed of strongly trigonally distorted SbBr octahedral anions and CHN dications.

Di(pyridin-2-yl)amino-substituted 1,10-phenanthrolines and their Ru(II)-Pd(II) dinuclear complexes: synthesis, characterization and application in Cu-free Sonogashira reaction.

Dinuclear complexes bearing Ru(II) photoactive centers are of interest for the development of efficient dual catalysts for many photocatalyzed reactions. Ditopic polypyridine ligands, bis(pyridin-2-yl)amino-1,10-phenanthrolines, containing an additional coordination site (bis(pyridin-2-yl)amine, dpa) at positions 3, 4 or 5 of the 1,10-phenanthroline core (Phen-3NPy2, Phen-4NPy2 and Phen-5NPy2) were synthesized. They were used as bridging ligands to obtain dinuclear complexes [(bpy)Ru(Phen-NPy2)PdCl](PF) (Ru(Phen-NPy2)Pd) in good yields stepwise complexation.

Quinoxaline-based azamacrocycles: synthesis, AIE behavior and acidochromism.

The development of luminescent molecular materials has advanced rapidly in recent decades, primarily driven by the synthesis of novel emissive compounds and a deeper understanding of excited-state mechanisms. Herein, we report a streamlined synthetic approach to light-emitting diazapolyoxa- and polyazamacrocycles NCOQ and NCQ ( = 3-10; = 2, 3; = 2-5), incorporating a 2,3-diphenylquinoxaline residue (DPQ). This synthetic strategy based on macrocyclization through Pd-catalyzed amination reaction yields the target macrocycles in good or high yields (46-92%), enabling precise control over their structural parameters.

Fine-Tuning of the Optical and Electrochemical Properties of Ruthenium(II) Complexes with 2-Arylbenzimidazoles and 4,4'-Dimethoxycarbonyl-2,2'-bipyridine.

A series of cyclometalated complexes of ruthenium (II) with four different substituents in the aryl fragment of benzimidazole was synthesized in order to study the effect of substituent donation on the electronic structure of the substances. The resulting complexes were studied using X-ray diffraction, NMR spectroscopy, MALDI mass spectrometry, electron absorption spectroscopy, luminescence spectroscopy, and cyclic voltammetry as well as DFT/TDDFT was also used to interpret the results. All the complexes have intense absorption in the range of up to 700 nm, the triplet nature of the excited state was confirmed by measurement of luminescence decay.

Stable Spiro-Fused Diarylaminyl Radicals: A New Type of a Neutral Mixed-Valence System.

A new type of neutral mixed-valence system was synthesized using a facile one-pot procedure. The spiro-conjugated framework is additionally "fastened" with a biphenyl bridge, which does not directly participate in spin delocalization but makes the molecule stable and influences the reorganization energy and the energy barrier of the intramolecular electron transfer. The in-depth experimental and quantum-chemical study allowed determining the radicals as the Class II Robin-Day-mixed-valence systems.

Synthesis, Crystal, and Electronic Structure of (HpipeH)[SbI](I), with I Molecules Linking SbX Dimers into a Polymeric Anion: A Strategy for Optimizing a Hybrid Compound's Band Gap.

In searching for a tool for optimizing the band gap of a hybrid compound capable of serving as a light-harvesting material in lead-free photovoltaics, we synthesized a new polyiodoantimonate (HpipeH)[SbI](I) and analyzed its crystal and electronic structure by application of X-ray crystal structure analysis, Raman and diffuse reflectance spectroscopies, and quantum chemical calculations. It was demonstrated that I molecules link SbI edge-sharing octahedra into zig-zag chains, whereas the organic cations link inorganic anionic chains into a 3D structure featuring a complex pattern of covalent bonds and non-covalent interactions. Overall, these features provide the background for forming the electronic structure with a narrow band gap of 1.

Mono- and Mixed Metal Complexes of Eu, Gd, and Tb with a Diketone, Bearing Pyrazole Moiety and CHF-Group: Structure, Color Tuning, and Kinetics of Energy Transfer between Lanthanide Ions.

Three novel lanthanide complexes with the ligand 4,4-difluoro-1-(1,5-dimethyl-1H-pyrazol-4-yl)butane-1,3-dione (HL), namely [LnL(HO)], Ln = Eu, Gd and Tb, were synthesized, and, according to single-crystal X-ray diffraction, are isostructural. The photoluminescent properties of these compounds, as well as of three series of mixed metal complexes [EuTbL(HO)] (EuTbL), [EuxGdL(HO)] (EuGdL), and [GdTbL(HO)] (GdTbL), were studied. The EuTbL complexes exhibit the simultaneous emission of both Eu and Tb ions, and the luminescence color rapidly changes from green to red upon introducing even a small fraction of Eu.