Response of Fluorescent Boron Difluoride β-Diketonates to X-Rays.

This paper reports the results of a detailed study of the optical response of boron difluoride curcuminoids to radiation exposure. Two lines of the dyes fundamentally different in structure (namely, symmetrical and asymmetrical) were tested. If the absorption responses of their solutions in chloroform to X-rays turns out to be quite close quantitatively (note that it has a very indicative visual manifestation - a gradual discoloration is observed in the dose range up to 300 Gy), the fluorescence ones differ notably: among other things, the former demonstrate much more sensitive reactions (the corresponding limit of detection values ​​differ by up to 2.

Exciplex luminescence of difluoroboron meta- and para-Nitrodibenzoylmethanates in solutions and polymer matrix.

Molecular systems with intense exciplex luminescence are promising for the creation of OLEDs and light-transforming materials. The luminescent properties of difluoroboron meta- and para-nitrodibenzoylmethanates (1 and 2) were studied by the steady-state and time-resolved luminescence spectroscopy methods and quantum chemistry simulation. The influence of the position of the nitro group on the spectral properties of the complexes was revealed.

Fluorescent boron difluoride curcuminoides as perspective materials for bio-visualization.

Curcuminoids of boron difluoride, 1-aryl(hetaryl)-5-phenylpenta-2,4-dien-1-onates of boron difluoride, have been synthesized. A comparative study of the electronic structure, luminescent properties and their potential for applications in bio-imaging has been carried out. The influence of the electronic structure of α-substituents on the luminescence of compounds was studied by the methods of stationary and time-resolved luminescence spectroscopy and DFT modeling.

Thermoluminescent Tb(III) and Dy(III) complexes with redox-active ligands: experimental and theoretical study.

Thermoluminescence and persistent luminescent materials with unique delayed emission have attracted much attention and exhibit great promise in optical information storage. In this manuscript, to reveal the thermoluminescence mechanism, a combined experimental and theoretical study of ternary Ln(NO ) Acac(Phen) complexes, where Ln is Tb(III), Dy(III), Eu(III), Acac is acetylacetonate anion, and Phen is 1,10-phenanthroline, was carried out. The terbium and dysprosium complexes had thermoluminescence properties, while the europium complex did not.

Polymer films doped with boron difluoride ortho-hydroxydibenzoylmethanates: Solvatochromism and solvent-induced exciplex formation.

The spectral properties and solvatochromic behavior of boron difluoride ortho-hydroxydibenzoylmethanates in polymer matrices with different polarity (polystyrene, polyvinyl chloride, polycarbonate, poly(methyl methacrylate)) were investigated. The specific interaction of polystyrene, polycarbonate and poly(methyl methacrylate) with the investigated fluorophores was revealed. It was shown that the dyes are capable to form exciplexes with phenyl rings of polystyrene.

Anthracene-containing complexes of boron difluoride. Dual luminescence, formation of excimers, and mechanochromism.

A comparative study of the luminescence properties and crystal structure of boron difluoride 1-(anthracen-9-yl)butane-1,3-dionate (1) and their nitrogen-containing analogs with hydrogen and methyl substituents (2 and 3) has been performed. For boron difluoride beta-diketonate (1) and beta-ketoiminate with a hydrogen substituent (2), which does not create significant steric difficulties, the luminescence of crystals is determined by that of excimers and aggregates based on them. For the compounds 1-3, mechanofluorochromism has been observed, the spectral manifestation of which is different: at grinding the crystals of 1 and 2, a hypsochromic shift of the excitation and luminescence bands occurs, whereas in the case of crystals of 3, a bathochromic shift takes place.

Optical properties and electronic structure of Eu(III) complexes with HMPA and TPPO.

Two adducts of Eu(III) tris-hexofluoroacetylacetonate with HMPA (OP(N(CH)), hexamethylphosphotriamide) and TPPO (OP(CH), triphenylphosphine oxide) were studied by optical spectroscopy and quantum chemistry (DFT/TD-DFT). The structure of the higher occupied molecular orbitals (MO) of the two adducts determines differences in the position of the excitation band maximum of hfac ligands. According to the calculation data, all excited states are caused by the transition to 3 vacant π* MOs of hfac ligands.

Unexpected luminescent and photochemical properties of europium(III) cinnamates - Theoretical and experimental study.

The luminescent and photochemical properties of europium(III) cinnamates [Eu(Cin)] (I) and Eu(Cin)·(phen) (II) were investigated in theoretical and experimental aspects. The high photostability of the complex I was explained. The complex II displays weak luminescence and low photostability in spite of the presence of a powerful antenna ligand 1,10-phenantroline in its coordination sphere.

o-Hydroxydibenzoylmethanate of boron difluoride: A complex with multi-stimuli-responsive emission effects.

The structural, luminescence and chemosensor properties of boron difluoride o-hydroxydibenzoylmethanate (1) have been investigated. In the concentrated solution, PE (polyethylene) matrix, and crystals of 1, one observes the formation of J-aggregates. The crystal structure of 1 is in compliance with that of J-aggregates of the "brickwork type" consisting of dimers that comprise excimer traps.

Halide Perovskite-Derived Compounds RbTeX (X = Cl, Br, and I): Electronic Structure of the Ground and First Excited States.

Herein, we report a study of the electronic structure of the ground and first excited states of RbTeCl, RbTeBr, and RbTeI halide-perovskite-derived crystals. Using X-ray photoelectron spectroscopy (XPS) measurements and density functional theory and multiconfiguration self-consistent field (MCSCF) calculations, the experimental and theoretical XPS spectra of the valence region were obtained. In addition, the effects of the cations and halogen atoms on the electronic structure were determined, and the classification of the excited states in double point group representation was carried out.

Spectroscopic and quantum chemical study of difluoroboron β-diketonate luminophores: Isomeric acetylnaphtholate chelates.

The electronic structure and optical properties of the isomeric difluoroboron β-diketonates, 2,2-difluoro-4-methylnaphtho-[2,1-e]-1,3,2-dioxaborin (I) and 2,2-difluoro-4-methylnaphtho-[1,2-e]-1,3,2-dioxaborin (II), were studied by means of X-ray photoelectron, absorption and luminescence spectroscopies. The experimental results were interpreted using high-level ab initio quantum chemical computations, including the algebraic-diagrammatic construction method for the polarization propagator of the second and third orders (ADC(2) and ADC(3)), the outer-valence Green's function (OVGF) method, and the time-dependent density functional (TDDFT) approach. The X-ray photoelectron measurements were assigned in the entire energy range using the results of the Kohn-Sham orbital calculations which employed the B3LYP functional.

Electronic structure and optical properties of Ln(III) nitrate adducts with 1,10-phenanthroline.

Adducts of tris-nitrates of rare-earth elements Ce(III), Nd(III), Eu(III), and Er(III) with two molecules of 1,10-phenanthroline with formula Ln(NO)(Phen) are studied by X-ray photoelectron spectroscopy (XPS) and quantum chemistry (DFT/TDDFT). The geometric structure for DFT modeling is build using X-ray diffraction data. To analyze the composition and differences of the electronic structure in the series under study, XPS spectra were obtained for which interpretation was performed using calculated data.

Europium(III) complex with powerful antenna ligands: Interligand interaction.

The luminescent properties of europium(III) trifluoroacetate [Eu(TFA)3bipy·3Н2О]∙bipy (I), where TFA - trifluoroacetate anion and bipy - 2,2'bipyridyl were investigated. Despite the presence of two efficient antenna ligands in complex (bipy1 in europium coordination sphere and bipy2 in the outer-sphere) the complex displays weak luminescence. By employing density functional theory-based methods, the luminescence, electron structure, interligand interactions and the processes of energy transfer in I were investigated.

Design, Synthesis, and Crystallization-Induced Emission of Boron Difluorides β-Ketoiminates.

A series of new nitrogen-containing analogues of boron difluoride benzoylacetonates with hydrogen and methyl substituents at the nitrogen atom have been synthesized. A comparative study of boron difluoride β-ketoiminates and their oxygen-containing analogues by means of luminescence and IR spectroscopic methods as well as quantum chemistry simulations was also performed.

Boron difluoride dibenzoylmethane derivatives: Electronic structure and luminescence.

Electronic structure and optical properties of boron difluoride dibenzoylmethanate and four of its derivatives have been studied by X-ray photoelectron spectroscopy, absorption and luminescence spectroscopy and quantum chemistry (DFT, TDDFT). The relative quantum luminescence yields have been revealed to correlate with charge transfers of HOMO-LUMO transitions, energy barriers of aromatic substituents rotation and the lifetime of excited states in the investigated complexes. The bathochromic shift of intensive bands in the optical spectra has been observed to occur when the functional groups are introduced into p-positions of phenyl cycles due to destabilizing HOMO levels.

Electronic structure and spectral properties of terbium(III) nitrate complex with hexamethylphosphoramide.

Spectral properties of terbium(III) nitrate complex with hexamethylphosphoramide have been studied by quantum-chemical methods within the density functional theory and methods of luminescent and X-ray photoelectron spectroscopy. Analysis of the luminescence excitation spectrum of the complex has indicated the absence of intramolecular transfer of electronic excitation energy from the ligand levels to the resonance levels of the rare earth central ion, so luminescence of the complex is associated with the electronic f-f-transitions of Tb ion (transitions D→F, J=3-6). According to quantum-chemical modeling of the excited singlet and triplet levels of the complex, the excitation energy transfer from the ligands onto the central ion does not occur because of the significant difference of energies of their excited states.

Electronic Structure and Optical Properties of Boron Difluoride Dibenzoylmethane Derivatives.

Electronic structure and optical properties of boron difluoride dibenzoylmethanate BF2Dbm and its four derivatives were studied using X-ray photoelectron spectroscopy, absorption and luminescence spectroscopy, and quantum chemistry (DFT and TDDFT). In a series of the studied compounds, the relationship of molecular design and optical properties has been revealed. At the transition from BF2Dbm to BF2Dbm(OCH3)2, the HOMO-LUMO energy gap decreases, resulting in a bathochromic shift of the optical spectra.

Triboluminescence and crystal structure of the complex [Eu(NО ) (HMPA) ]: role of cleavage planes.

The atomic structure of crystals of the [Eu(NО ) (HMPA) ] [hexamethylphosphotriamide (HMPA)] complex characterized by an intensive luminescence and triboluminescence was determined using X-ray structural analysis. Noncentrosymmetric crystals have a monoclinic syngony: a = 16.0686 (3), b = 11.

Nitrogen-Containing Analog of Dibenzoylmethanate of Boron Difluoride: Luminescence, Structure, Quantum Chemical Modeling, and Delay Fluorescence.

Boron difluoride of 3-amino-1,3-diphenyl-2-propene-1-onate (1) has been synthesized and its crystal structure has been determined. The comparative studies of 1 and its oxygen analog 1,3-diphenyl-1,3-dionate (dibenzoylmethanate) of boron difluoride (2) have been performed using the methods of stationary and time-resolved spectroscopy and quantum chemical modeling. It was established that at the transition from solutions to crystals, a bathochromic shift of the spectra and a significant increase of luminescence intensity of 1 take place.

Laser printing of resonant plasmonic nanovoids.

Hollow reduced-symmetry resonant plasmonic nanostructures possess pronounced tunable optical resonances in the UV-vis-IR range, being a promising platform for advanced nanophotonic devices. However, the present fabrication approaches require several consecutive technological steps to produce such nanostructures, making their large-scale fabrication rather time-consuming and expensive. Here, we report on direct single-step fabrication of large-scale arrays of hollow parabolic- and cone-shaped nanovoids in silver and gold thin films, using single-pulse femtosecond nanoablation at high repetition rates.

Triboluminescence and crystal structure of the centrosymmetric complex [Tb(NO ) (Acac)(Phen) ]·H O.

The atomic structure of crystals of the complex [Tb(NO ) (Acac)(Phen) ]·H O, (AA - acetylacetonate anion, Phen - 1,10-phenanthroline) characterized by an intensive luminescence and triboluminescence has been determined by means of an X-ray structural analysis method. Centrosymmetric crystals have a monoclinic syngony: a = 11.2298(1), b = 9.

Europium(III) tris-dibenzoylmethanate as an efficient chemosensor for detection of ammonia.

The effect of ammonia vapor on luminescence of Eu(III) tris-dibenzoylmethanate immobilized in various matrices has been investigated. It has been revealed that interaction of Eu(III) tris-dibenzoylmethanate with analyte vapor results in increase of the intensity of Eu(III) luminescence. The mechanism of the effect of ammonia vapors on intensification of the Eu(III) luminescence has been suggested using the data of IR spectroscopy, X-ray diffraction analysis and quantum chemistry calculations.

Luminescence of solvate of boron difluoride dibenzoylmethanate with benzene: aggregates formation.

The concentration dependence of spectral-luminescence properties of solutions boron difluoride dibenzoylmethanate (DBMBF2) in benzene and chloroform has been studied through stationary and time-resolved emission spectroscopy methods. The formation of J-aggregates in the solution of DBMBF2 in chloroform has been revealed and a crystalline adduct of DBMBF2 with benzene has been obtained. A bright blue adduct luminescence is due only to the luminescence of J-aggregates, unlike the crystals of DBMBF2, for which the luminescence of excimers and J-aggregates has been observed.