Resumo em Inglês:

This review summarizes investigations carried out at the Laboratory of Photochemistry and Energy Conversion (LFCE) in the University of São Paulo dealing with design and characterization of ruthenium(II), rhenium(I) and iridium(III) polypyridine complexes with desired photochemical and photophysical properties in light of the development of optoelectronics and photoinduced energy conversion systems. First, the breakthroughs on molecular engineering of emissive ReI, RuII and IrIII complexes for the development of highly efficient light-emitting devices, such as organic light-emitting diodes (OLEDs) and light-emitting electrochemical cells (LECs), are presented. Then, the photochemical and photophysical properties of fac-[Re(CO)3(NN)(trans-L)]+ complexes (NN = bidentate polypyridyl ligands and trans-L = stilbene-like ligand), which find use in molecular machines and photosensors, are discussed. Finally, dye-sensitized energy conversion devices based on RuII complexes and natural dyes, such as dye-sensitized solar cells (DSCs) and dye-sensitized photoelectrosynthesis cells (DSPECs), are reviewed, highlighting some strategies for photoanode engineering aiming at improved device efficiencies.

Resumo em Inglês:

Hybrid-peptide hydrogel arrangements are a promising alternative to obtaining biocompatible structures at the nanoscopic scale. In this work, a new class of hybrid hydrogels was obtained through the sol-gel process based on the reaction between an amyloid-like octapeptide sequence [RF]4 (where R = arginine and F = phenylalanine) covalently bonded with glycine-linked alkoxysilanes, and hybrid silylated polyethylene glycol (PEG). 1H nuclear magnetic resonance (NMR), liquid chromatography-mass spectrometry (LC-MS), and Fourier transform infrared spectroscopy (FTIR) analyses were used, resulting in synthesized precursor/intermediate molecules. The structure of hybrid hydrogel fibers was studied by atomic force microscopy (AFM) and small-angle X-ray scattering (SAXS), where the existence of two regions in the Guinier plot was observed, one being predominantly formed by polymer while the other one by peptide chains. The rheological measurements showed that viscoelastic parameters depend on both the amount of silane peptide in the hydrogel matrix and increased temperature. Also, the FTIR spectra indicated the coexistence of antiparallel and parallel β-sheet structure patterns into amyloid fibril hydrogels, which can be modulated by peptide-silane coupling in each formulation. The analyzed hydrogels showed thixotropic and shear-thinning rheology at physiological pH, leaving open the opportunity to topical drug delivery system applications in the future.

Resumo em Inglês:

Synthetic conditions were evaluated to intercalate norbixin into layered double hydroxides (LDH). Norbixin was isolated from a hydrosoluble commercial annatto extract. LDH samples comprising M2+/Al3+ (M = Mg, Zn) were synthesized by coprecipitation and characterized by X-ray diffraction, thermal analysis coupled to mass spectrometry, vibrational spectroscopies, and solid-state 13C nuclear magnetic resonance. Radical scavenging activity of LDH hybrids was monitored by electron paramagnetic resonance towards the stable radical DPPH (1,1-diphenyl-2-picrylhydrazyl). LDH hosts presented more than 50 wt.% of norbixin and d-spacing (003) values of about 2.5 or 3.0 nm depending of the cation LDH composition. Vibrational spectra assignment (supported by density functional theory calculations) confirmed the chemical integrity of norbixin after intercalation into LDH. The inorganic layers were found to enhance the thermal stability of norbixin upon intercalation. The free radical scavenging capacity of norbixin was retained when immobilized into LDH. Considering that zinc and magnesium-LDH matrices are biocompatible and that norbixin presents biological activity, the hybrid materials appear as promising systems for biomedical assessment.

Resumo em Inglês:

The pyrolysis of waste tire has been proposed as an alternative route to its recycling producing residual oils that can be used as fuels. In this work, a physicochemical process to obtain carbon-based dots (CBD) from carbon black (CBL) derivatives of tires is described. For this, the CBL was treated with different acids to produce CBL1 and CBL2 particles suspension. The pH of the suspension was adjusted to 5.6 to precipitate remaining impurities. Afterwards, the supernatant was ultra-centrifuged and the yellow pale solid, the purified CBD obtained by roto evaporation, was characterized by ultraviolet-visible spectrophotometer (UV-Vis), photoluminescence (PL) at 320-380 nm, high-resolution transmission electron microscopy (HRTEM), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), energy-dispersive X-ray spectroscopy (EDX), Fourier transform infrared microscopy (mFTIR), and X-ray photoelectron spectroscopy (XPS). This material showed the typical excitation wavelength dependent emission and a PL quantum yield of 19.29% and was constituted by a well-defined spherical shaped and single sheets of “graphene quantum dots” with undefined shape, with potential applications in optoelectronic and fluorescence imaging devices.

Resumo em Inglês:

Bambus[n]uril synthesis may be challenging, and it is frequently achieved with low purity and low yields. We have studied the effect of different anions on the synthesis of bambus[6]uril, especially in terms of yield, exploring template effects driven by anions in the reaction medium. The influence of the anions is evident on such syntheses and ClO4− particularly led to unprecedented synthesis yields. Computational calculations have also been used to elucidate the influence of anions on cyclization process.

Resumo em Inglês:

Mononuclear and binuclear RuII/arene/triphenylphosphine complexes with p-substituted benzoic acid derivatives were prepared and characterized. These monocationic complexes of type [Ru(η6-p-cymene)(PPh3)L] (L = benzoic acid (1), p-hydroxybenzoic acid (2), p-nitrobenzoic acid (3) and terephthalic acid (4)) were characterized using various techniques, such as nuclear magnetic resonance (NMR) and matrix-assisted laser desorption/ionization-time of flight (MALDI-TOF) mass spectrometry, and the crystal structure of 1, 3 and 4 were determined by X-ray diffraction analysis. The cytotoxicity of the complexes was evaluated, in vitro, against tumorigenic [MDA-MB-231, MCF-7 (breast), A549 (lung) and DU-145 (prostate)] and non-tumorigenic [MCF-10A (breast), MRC-5 (lung) and PNT-2 (prostate)] cells. The binuclear complex (4) was inactive due to its low solubility. Complexes 1, 2 and 3 showed similar cytotoxicity, however, complex 1 presented better selectivity index against MDA-MB-231 than compounds 2 and 3. Cellular ruthenium absorption was explored by inductively coupled plasma mass spectrometry (ICP-MS) analyzing the whole cells and the culture medium. Complementary studies showed that complex 1 inhibited colony formation, induced morphology changes in cells and promoted cell cycle arrest in the Sub-G1 phase for the MDA-MB-231 cells.

Resumo em Inglês:

A new series of tris-(bipyridyl)ruthenium-like complexes based on the 4-tripheylamine-2,2’:6’,2’’-terpyridine (TPA) push-pull ligand was prepared by incorporation of 4-carboxypyridine (cpy), 4,4’-dicarboxi-2,2’-bipyridine (dcbpy) and 4-carboxyterpyridine ligands (ctpy) ligands, in order to adsorb them on TiO2 in different anchoring conformations. The electron photoinjection and electron recombination processes of the respective dye-sensitized solar cells were greatly influenced by the molecular structure, which defined the surface concentration and surface charge on TiO2, such that the photoconversion efficiency was 10 times larger for [Ru(py)(dcbpy)(TPAtpy)] than for the [Ru(cpy)(bpy)(TPAtpy)](PF6) dye. Molecules anchoring in a more upright position and by a larger number of sites were shown to enhance the electron injection into TiO2 conduction band (CB) improving the short-circuit current (JSC), open circuit voltage (Voc) and the overall photoconversion efficiency. However, a positive net charge in the dye increased the back electron-transfer reactions and induced a decrease in both Voc and conversion efficiency.

Resumo em Inglês:

The combination of white or colorless oxides (MgO, Al2O3, ZnO) with colorant ions (Co2+) generates colored pigments (pink, blue, green). The color is caused by the insertion of the colorant ion in the respective crystal lattices (periclase, alumina, wurtzite), as verified by X-ray diffraction. Absorption spectra in the visible region show analogous triplet behavior of the absorption bands for the doped alumina and wurtzite samples but a difference in tetrahedral distortion, which generates blue and green pigments. In contrast, cobalt-doped periclase has color-related parameters related to the pink color. Crystallite and particle sizes show nanometric dimensions in the range of 20-60 nm (magnesium), 20-180 nm (aluminum), and 40-220 nm (zinc). The color is related to the shape (crystalline phase), size, and presence of chromophore ions with absorption in the visible region. Colorimetric studies (CIE L*a*b*) show variations between colors as a function of the polysaccharide that is used (starch or pectin) as fuel. The color variation is subtle in some cases but is significantly noticeable in other cases. Commercial colorless ink dispersion (10% m/m) shows excellent compatibility with the maintenance of hues and a slight increase in color saturation (C*).

Resumo em Inglês:

An electrocatalytic active hybrid material prepared by successive stepwise coordinative deposition of 20 nm diameter gold nanoparticles (AuNP) with 5,10,15,20-tetra(4-pyridyl)-21H,23H-porphine (TPyP) on fluorine-doped tin oxide (FTO) substrates previously modified with 3-mercaptopropylsilane is described. Their interaction and assembly were studied by UV-Vis spectroscopy and surface enhanced Raman spectroscopy to understand the kinetics as well as the conformation on the porphyrin macrocycle on the electrode surface as a function of its concentration. The hybrid nanomaterial was a build-up in reproducible successive deposition steps as confirmed by the linear rise of the absorption bands assigned to AuNP and TPyP as a function of the number of AuNP/porphyrin hybrid deposition steps, as supported by scanning electron microscopy (SEM) images. Electrodes modified with the hybrid nanomaterials were prepared and characterized by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), as well as their electrocatalytic properties for the oxidation of nitrite and sulfite investigated. FTO electrodes modified with the AuNP/TPyP hybrid showed remarkable electrocatalytic activity as confirmed by reproducible and sensitive amperometric responses for sensing nitrite and sulfite in comparison to the bare electrode while reducing overpotentials respectively to 0.8 and 0.4 V and improving the dynamic range (linear response allowing quantification in the 50 to 500 µmol L-1 range) for detection of analytes.

Resumo em Inglês:

The free-base meso-tetra(4-pyridylvinylphenyl)porphyrin (1a) and its zinc(II) complex were synthesized and then functionalized with [Ru(bpy)2Cl]+ units (2a and 2b) via conventional methods and evaluated in terms of photophysical, electrochemical and biological aspects. All porphyrins present moderate singlet oxygen production and fluorescence quantum yield, and did not show any aggregation process. The photo-oxidation ability of those porphyrins decreased in the order 2b > 1a > 2a. The electrochemical behavior of 2a and 2b modified electrodes was evaluated by electroanalytical methods. Also the 2b electrode showed a smaller charge transfer resistance (36.70 Ω) when compared to 2a electrode (45.17 Ω). In addition, even after 30 consecutive injections of nitrite solution (1.0 × 10−4 mol L−1) using the flow injection analysis (FIA) system, the modified 2b electrode showed an relative standard deviation (RSD, n = 30) of 1.36% exhibiting a great potential as amperometric sensor for nitrite. Moreover, the biological evaluation towards human serum albumin (HSA) indicated spontaneous, weak and ground-state association in the IB subdomain (site III) and possibily a second site, changing the conventional interaction mode of porphyrins with biomolecules as consequence of the longer arms (porphyrin ring substituents at meso-positions) ending with a ruthenium polypyridyl complex, that may enhance the photodynamic therapy (PDT) efficiency of photogenerated reactive oxygen species (ROS) species.

Resumo em Inglês:

A new dinuclear complex of formula [{Re(CO)3(py)}2(µ-4,4”-azobpy)](PF6)2, with py = pyridine and 4,4”-azobpy = 4,4”-azobis(2,2’-bipyridine), has been synthesized and characterized by spectroscopic and electrochemical techniques. The symmetrical nature of the dimetallic cation has been confirmed by nuclear magnetic resonance (NMR) measurements. When adding L-cysteine or L-glutathione, large and rapid changes in its UV-Vis absorption spectra were observed, which can be used for detecting both biologically relevant thiols. A promising activity for using this complex as a chemotherapeutic agent for bone cancer was also disclosed. Quantum mechanical calculations supported the experimental data.

Resumo em Inglês:

The water oxidation is the limiting step in the water-splitting process. Given this scenario, the development of new catalysts is essential in this field. The emergent demand is the use of Earth-abundant elements and catalysts with high performance under mild conditions. Because of this, catalysts such as Prussian Blue analogues (PBA) have been receiving a lot of attention in recent years. In addition, working under neutral conditions allows us to take advantage of the modification of conductive polymeric 3D printed electrodes (3DPE) with Prussian Blue. Thus, we described in this work the development of the polymeric 3D printed electrodes modified by cobalt-Prussian Blue and their performance in the water oxidation process. The 3D printed electrodes modified with Co3[Co(CN)6]2 (Co-Co PBA) have a Tafel slope of 343 mV dec−1 while those modified with Co3[Fe(CN)6]2 (Co-Fe PBA) have a Tafel slope of 378 mV dec−1. This means that both catalysts have the same mechanism for the water oxidation process. On the other hand, the overpotential of Co-Co PBA in 3DPE is lower than the value observed by Co-Fe PBA in 3DPE suggesting the best electrocatalytic activity for Co-Co PBA catalyst.

Resumo em Inglês:

This work presents the NO release from compound [Ru(biq)2(H2O)(NO)](PF6)3 (biq = 2,2’-biquinoline) with visible light irradiation (λirrad = 660 nm), assisted by the low-absorbing photosensitizer [Ru(biq)2Cl2]. The structure of both compounds were characterized by means of ESI-MS (electrospray ionization mass spectrometry). The NO+ stretching, ν(NO) = 1995 cm-1, is atypically shifted to higher energy. This observation, along with the E1/2 = 0.49 V (vs. Ag/AgCl) assigned to the Ru2+/3+ redox pair observed for compound [Ru(biq)2Cl2] and its photoreactivity in solution suggest that the RuII ion, when coordinated to two biquinolines, behaves as a hard Pearson acid. Molecular modelling results confirmed the typical geometry distortion of ruthenium-polypyridine complexes bearing sterically hindered ligands. They also suggest the formation of a supramolecular dimer, assembled by weak interaction between biquinoline ligands from each compound, that is claimed to be responsible for the high efficiency of the NO photorelease bimolecular sensitization.

Resumo em Inglês:

The diruthenium(II,III)-ibuprofen (RuIbp) metallodrug shows anticancer activity in vitro and in vivo. The encapsulation into lipid nanoparticles enhanced the efficacy in glioblastoma, breast and prostate cancer cells. Here we report data for RuIbp hydrophobicity, solubility in alcohol/water, and behavior in 1-5% ethanol/water and ethanol/cell culture medium. RuIbp is capable of spontaneously generate self-assembled RuIbpNP nanoparticles when drug ethanolic solutions are added to water or cell growth culture medium at 1-5% ethanol. The phenomenon was investigated, and the nanoparticles characterized. RuIbpNP nanoparticles formed at 100-200 µmol L−1 RuIbp are colloidally stable and nearly spherical showing zeta potential about +40 mV and particle size about 100 (aqueous suspension) and 180 nm (culture medium). The integrity of the [Ru2(Ibp)4] framework was confirmed by spectroscopy and mass spectrometry. Significant amount of metallodrug was found in suspension (85%, culture medium; 54%, culture medium with cells). The uptake by U87MG glioblastoma cells was 6% at 24 h. The spontaneous nanosizing of RuIbp in the form of nanosuspensions may explain the biological activity of this highly hydrophobic metallodrug. The present findings expand the knowledge on the behavior of RuIbp, opening new directions to exploit the properties of the metallodrug targeting cancer therapy.

Resumo em Inglês:

Minimizing the emission of industrial effluents and realizing the recovery/extraction of key elements such as the rare earths from low concentration solutions, or during water decontamination processes, are some of the biggest challenges of modern society. Accordingly, the preparation and characterization of a low cost recyclable and reusable superparamagnetic iron oxide nanoparticles (SPION)/zeolite nanocomposite (Zmag) is described, and the possibility of their use for removal of heavy metals and ammonium/ammonia is discussed, generating water whose quality is in compliance with the more strict modern environmental laws. Such materials are suitable for realization of a more efficient dispersion method for adsorption in combination with magnetically aided concentration/separation processes for removal of contaminants. In fact, Zmag was shown to efficiently remove PbII and HgII, as well as NH4+ from water, generating effluents that can be directly disposed in water bodies according to the current environmental law requirements, as stated by EPA (North America Environmental Protection Agency). That nanocomposite material has a competitive production cost and allowed a cutback in the nitrogen (NH3) content from 300 mg L-1 (diluted slurry source) to less than 36 mg L-1. Furthermore, Zmag demonstrated high capacity to concentrate and recover in a cyclic way LaIII.

Resumo em Inglês:

A new nickel based layered double hydroxide nanomaterial, Ni0.8Ce0.2-LDH, constituted by about 3 nm large nanoparticles exhibiting enhanced electrocatalytic properties towards oxidation of glycerol in alkaline media, was prepared by incorporation of 20 wt.% of CeIII ions into α-nickel hydroxide. This can be oxidized to CeIV, as demonstrated by X-ray photoelectron spectroscopy, a much electron withdrawing and oxidizing species responsible for electronic interactions and additional electrocatalytic active sites giving rise to synergic effects. High-resolution transmission electron microscopy images and the X-ray diffractograms indicated a material with a significantly lower size and degree of crystallinity than α-Ni(OH)2, one of the factors contributing to its enhanced electrochemical and electrocatalytic activity, as demonstrated by cyclic voltammetry and electrochemical impedance spectroscopy, suggesting a good potentiality for development of glycerol fuel cells.

Resumo em Inglês:

This article discusses the use of density functional theory (DFT) calculations in classifying and characterizing bimetallic ruthenium mixed-valence systems in terms of their electronic localization/delocalization degree. A standard B3LYP/LanL2DZ methodology including integral equation formalism-polarizable continuum model (IEF-PCM) solvent model is evaluated for a set of 16 non-symmetric mixed-valence cyanide-bridged ruthenium polypyridines. This procedure reproduces well the features of the observed electronic and vibrational spectra, with better agreement for the more delocalized systems, and therefore provides an appropriate description of the electronic structures. Computed spin densities support class II or class III Robin-Day assignments and allow to quantify the electronic delocalization degree. The applied methodology yields good results due to the nature of the systems explored, which display a strong electronic coupling promoted by the cyanide-bridge and a lack of strong specific solvation effects. This procedure is not only useful in the study of ground state mixed-valence systems, but also provides a powerful insight into photoinduced mixed-valence excited states of related complexes.

Resumo em Inglês:

The molecular control in Langmuir-Blodgett (LB) films may be exploited in charge storage electrodes provided a suitable choice of molecular architecture and components is made. In this paper, we employed a naphtyl-1,3,4-oxadiazole amphiphile (NFT1) and its complex [Ru(bpy)2NFT1]PF6 (RuNFT1) (bpy = 2,2’-bipyridine) in heterostructured LB films in a proof-of-principle production of charge storage. The optimized architecture contained a one-layer RuNFT1 deposited on a 9-layer NFT1 LB film, where the efficient packing of NFT1 inferred from spectroscopic measurements and Brewster angle microscopy (BAM) images was considered as relevant for ion diffusion. This packing was achieved owing to the π-stacking warranted by the planarity of the NFT1 naphtyl 1,3,4-oxadiazole ring, as confirmed with density functional theory (DFT) calculations. The top layer of the redox-active RuNFT1 provided an additional contribution with its Faradaic charge storage to the double layer capacitance of NFT1. Taken together, these results demonstrate that synergy may be achieved in combining distinct compounds in LB films toward efficient charge storage.

Resumo em Inglês:

In this study, new perylene-derived molecules were synthesized as perylene-3,4,9,10-tetracarboxylic acid monoanhydride monopotassium carboxylate 1; N-(3-propanol)perylene-3,4,9,10-tetracarboxylic-3,4-(monoimide)anhydride-9,10-acid potassium carboxylate 2; 5,11,17,23-tetra(tert-butyl)-25,27-bis(3’-bromopropoxy)-26,28-(dihydroxy)calix[4]arene 3; 5,11,17,23-tetra(tert)butyl)-25-(3’-bromopropoxy)-27-(N-[3’(3’-propoxy)propyl]perylene-(3’,4’,9’,10’-tetracarboxylic-3’,4’-(monoimide)anhydride-9’,10’-acid potassium carboxylate)-26,28-(dihydroxy)calix[4]arene 4. They were characterized by nuclear magnetic resonance (1H NMR, 1H-1H correlation spectroscopy (COSY), 1H-13C heteronuclear single quantum coherence spectroscopy (HSQC), 1H-13C heteronuclear multiple bond correlation (HMBC)), Fourier transform infrared (FTIR), UV-Vis, and luminescence spectroscopies, besides elemental analysis. Cyclic voltammetry and spectroelectrochemical behavior techniques showed a well-defined one-electron reversible process. The compounds have high emission quantum yield and are very stable electron-receptors. Ligand 4 has a broad emission shifted to 540 nm based on its precursor 2, shown at 531 nm. However, ligand 4 (φ = 0.31) depicted a quantum yield lower than compound 2 (φ = 0.57), indicating that association with calixarene slightly decreases quantum yield. Nevertheless, it improves solubility significantly in organic solvents, which renders it useful for applications in the development of organic light-emitting diode (OLEDs) or biological markers.

Resumo em Inglês:

In this paper a novel supramolecular strategy to improve the efficiency of a voltammetric sensor to determine two biologically relevant molecules (epinephrine (EP) and uric acid (UA)) is presented. The strategy is based on the use of a glassy carbon electrode modified with a copper(II) complex ([Cu(H2dimpy)Cl]PF6) adsorbed on multi-walled carbon nanotubes (MWCNTs). The [Cu(H2dimpy)Cl]PF6/MWCNT composite-supported electrode was characterized by electrochemical impedance spectroscopy, scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS). The electrocatalytic oxidation of EP and UA using the sensor was investigated by cyclic voltammetry and square wave voltammetry. Under optimized conditions, voltammetric peak currents showed a linear response for the EP and UA concentrations in the ranges 0.5-159.2 and 0.2-58.5 µmol L−1, whereas the limits of detection were 0.2 and 0.05 µmol L−1, respectively. The sensor was successfully applied in the selective and simultaneous determination of EP and UA in human urine samples. Thus, our results showed that the supramolecular strategy was successful to build an efficient sensor for simultaneous detection of these molecules in biological samples.

Resumo em Inglês:

The [Zn3(BTC)2·12H2O] (BTC = 1,3,5-tricarboxylate) metal-organic framework (MOF) was successfully synthesized using a microwave-assisted hydrothermal synthesis technique, which allowed for significantly decreased reaction time compared to the production of the same compound via conventional heating. In situ doping with Eu3+ ions at concentrations ranging from 1.0 to 5.0 mol% produced doped materials whose emission ranged from blue to red color. The Eu3+ spectroscopic properties were used to study the incorporation of the dopant into the structure of [Zn3(BTC)2·12H2O], even at very low concentrations. These experiments confirmed the usefulness of this ion as a luminescent probe, as it permitted the identification of small variations in structure not perceptible by X-ray diffraction. The variation in the coordination environment induced by increases in doping percentage was analyzed by evaluating changes in the characteristic Eu3+ excitation and emission profiles, using them to calculate luminescence lifetimes, experimental intensity parameters Ωλ (λ: 2 and 4) as well as the intrinsic quantum yield (QEu+3Eu+3) of the 5D0 emitting level of each doped MOF. The excitation and luminescence spectra show that intramolecular energy transfer from the BTC linker to Eu3+ ion, and we could observe the emission color tuning originated from the emissions of the BTC ligand and Eu3+ ion.

Resumo em Inglês:

Under simulated solar irradiation in the visible spectral region, the catalytically active RuIV-oxo species [Ru(O)(bpy)(tppz)]2+ (tppz = tetrapyridylpyrazine, a strongly π-accepting tridentate N, N, N-ligand) is produced directly from a single metal-to-ligand charge-transfer (MLCT) photoexcitation of the resting RuII-aquo complex [Ru(H2O)(bpy)(tppz)]2+ in aqueous media containing an electron acceptor. This photoinduced path to 2-electron/2-proton activation of a mononuclear catalyst (i.e., without a paired chromophoric unit) is enabled by the thermodynamic instability of the intermediate RuIII-hydroxo species [Ru(OH)(bpy)(tppz)]2+, which promptly disproportionates into the RuIV-oxo and RuII-aquo states as electrochemically observed by cyclic and pulse voltammetries in a wide range of pH. The proton-coupled multielectron photocatalytic capability of the complex in neutral aqueous solutions, at room conditions, was demonstrated through the dehydrogenative oxidation of benzyl alcohol into benzaldehyde with a product selectivity of about 100%. The performance of this mononuclear complex acting as chromophore/catalyst is comparable to that of the previously reported dinuclear complex [(tpy)Ru(tppz)Ru(HxO)(bpy)]4+. In addition to the characterization of redox and spectroscopic properties for the [Ru(L)(bpy)(tppz)]n+ derivatives with L = Cl- or HxO, structural analysis of the precursor chloro complex [RuCl(bpy)(tppz)](PF6) was also performed by single-crystal X-ray diffraction in this work.

Resumo em Inglês:

MWO4 host matrices (M: Sr, Ba) doped with different Tm3+ concentrations (0.02, 0.04, 0.06, 0.08 and 0.10 mol%) have been successfully prepared by the coprecipitation method at room temperature. The as-prepared nanophosphors were characterized by infrared spectroscopy showing intense absorption bands in the range of 700-1000 cm-1 attributed to the symmetrical and asymmetrical stretching vibrations (ν) of the tetrahedral [WO4]2- group. The X-ray diffraction (XRD) measurements reveal the tetragonal scheelite phase with the I41/a (No. 88) space group. The emission spectra of the MWO4:Tm3+ materials are dominated by the highest intensity narrow band of the intraconfigurational 1D2 → 3F4 transitions in the blue region (ca. 456 nm) arising from the Tm3+ ions. Additional low-intensity emission bands originated from the 1G4 → 3H6 (ca. 475 nm), 1G4 → 3F4 (660 nm) and 3H4 → 3H6 (700 nm) transitions are also observed. These optical results indicate that the materials can be used as an alternative to blue-emitting markers.