2D Cu(I)-I Coordination Polymer with Smart Optoelectronic Properties and Photocatalytic Activity as a Versatile Multifunctional Material.

This work presents two isostructural Cu(I)-I 2-fluoropyrazine (Fpyz) luminescent and semiconducting 2D coordination polymers (CPs). Hydrothermal synthesis allows the growth of P-1 space group single crystals, whereas solvent-free synthesis produces polycrystals. Via recrystallization in acetonitrile, P21 space group single crystals are obtained. Both show a reversible luminescent response to temperature and pressure. Structure determination by single-crystal X-ray diffraction at 200 and 100 K allows us to understand their response as a function of temperature. Applying hydrostatic/uniaxial pressure or grinding also generates significant variations in their emission. The high structural flexibility of the Cu(I)-I chain is significantly linked to the corresponding alterations in structure. Remarkably, pressure can increase the conductivity by up to 3 orders of magnitude. Variations in resistivity are consistent with changes in the band gap energy. The experimental results are in agreement with the DFT calculations. These properties may allow the use of these CPs as optical pressure or temperature sensors. In addition, their behavior as a heterogeneous photocatalyst of persistent organic dyes has also been investigated.

Efficient fluorescent recognition of ATP/GTP by a water-soluble bisquinolinium pyridine-2,6-dicarboxamide compound. Crystal structures, spectroscopic studies and interaction mode with DNA.

The new dicationic pyridine-2,6-dicarboxamide-based compound 1 bearing two N-alkylquinolinium units was synthesized, structurally determined by single-crystal X-ray diffraction, and studied in-depth as a fluorescent receptor for nucleotides and inorganic phosphorylated anions in pure water. The addition of nucleotides to 1 at pH = 7.0 quenches its blue emission with a selective affinity towards adenosine 5'-triphosphate (ATP) and guanosine 5'-tripohosphate (GTP) over other nucleotides such CTP, UTP, ADP, AMP, dicarboxylates and inorganic anions. On the basis of the spectroscopic tools (1H, 31P NMR, UV-vis, fluorescence), MS measurements and DFT calculations, receptor 1 binds ATP with high affinity (log K = 5.04) through the simultaneous formation of strong hydrogen bonds and π-π interactions between the adenosine fragment and quinolinium ring with binding energy calculated in 8.7 kcal mol-1. High affinity for ATP/GTP is attributed to the high acidity of amides and preorganized rigid structure of 1. Receptor 1 is an order of magnitude more selective for ATP than GTP. An efficient photoinduced electron transfer quenching mechanism with simultaneous receptor-ATP complexation in both the excited and ground states is proposed. Additionally, multiple spectroscopic studies and molecular dynamics simulations showed that 1 can intercalate into DNA base pairs.

Stokes and upconverted luminescence in Er3+/Yb3+-doped Y3Ga5O12 nano-garnets.

The green, red, near-infrared and near-infrared-to-visible upconverted luminescence properties of Er3+/Yb3+ codoped Y3Ga5O12 nanocrystalline powders have been studied using laser spectroscopy. A diffuse reflectance and luminescence spectra confirm that Er3+ and Yb3+ ions occupy the Y3+ sites of the single-phase cubic nano-garnet. Very bright green and red luminescence of the Er3+ ions are detected by the naked eyes, even for a laser power as low as 15 mW, when the Yb3+ ions are excited at 970 nm. The red upconverted emission is more intense than that under direct excitation of the Er3+ ions. The power dependence and the dynamics of the near-infrared-to-green and near-infrared-to-red upconverted emissions show the existence of different two-photon energy transfer upconversion processes. The results here presented indicate that Er3+/Yb3+ codoped Y3Ga5O12 can be a good candidate as an optical nanoheater and nanothermometer in biomedicine applications in the first biological window.

Condiciones sanitarias del albergue "COPACO" del bañado norte de Asunción, Paraguay (2018) / Sanitary conditions of the "COPACO" quarantine facility in the northern riverside slum of Asuncion, Paraguay (2018)

Los migrantes son más susceptibles a las enfermedades infecciosas, por las malas condiciones sanitarias donde viven. El objetivo fue describir las condiciones sanitarias del albergue "COPACO" del Bañado Norte en el 2018. Estudio descriptivo, transversal y temporalmente prospectivo. Fueron georreferenciados, ubicación y cantidad de grifos, sanitarios, desechos no biológicos, y medidas las distancias entre el agua potable y los desechos. Se evaluó el acceso y calidad del agua potable almacenada y fueron encuestadas las familias para conocer las enfermedades más prevalentes. Las referencias fueron las establecidas en el Manual ESFERA. Fueron contabilizadas 481 familias (2,405 personas); censados 22 baños químicos, 25 grifos, 5 puestos de ducha y 4 puntos de acumulación de desechos. El rango de distancia entre los baños y los 4 grifos más cercanos fue de 1 a 78 m, promedio 28 m. La distancia promedio entre el acúmulo de basura y los 4 grifos más cercanos fue de 21,1 m, rango 1 a 35 m. Cada grifo fue utilizado por 96 personas, 60% (9) de las familias almacenaban agua. Un baño móvil, con retrete y sin ducha era utilizado por 109 personas. Los baños eran unisex (mixtos) y carecían de fuente de agua y se improvisaron 5 puestos para ducharse, de utilización familiar. Fueron encuestadas 15 familias (3,1%). El promedio de estadía 33,3 días, 3 familias acusaron padecer de vómito, fiebre, diarrea y dolor dental. Los resultados pueden orientar a las autoridades sobre las futuras acciones a realizar para salvaguardar la salud de la población migrante

Migrants are more susceptible to infectious diseases, due to the poor sanitary conditions they live in. The objective of this work was to describe the sanitary conditions of the "COPACO" shelter in Bañado Norte (North Slum) in 2018. This was a descriptive, cross-sectional and temporally prospective study. The location and quantity of taps, toilets, non-biological waste were georeferenced, and the distances between drinking water and garbage were measured. Access and quality of stored drinking water were evaluated and families were surveyed to find out the most prevalent diseases. The references were those established in the SPHERE handbook. The number of families counted were 481 (2,405 people), 22 chemical toilets, 25 taps, 5 shower stalls and 4 garbage accumulation points were registered. The distance range between the toilets and the 4 closest taps was 1 to 78 m, average 28 m. The average distance between the garbage accumulation points and the 4 closest taps was 21.1 m, the range was 1 to 35 m. Each tap was used by 96 people, while 60% (9) of the families store water. A portable bathroom, with a toilet and without a shower, was used by 109 people. The bathrooms were unisex (mixed) and lacked a water source and 5 stalls were improvised for showering, for family use. Fifteen families were surveyed (3.1%). The average stay in the facilities was 33.3 days, and 3 families reported suffering from vomiting, fever, diarrhea and dental pain. The results can guide authorities on future actions to be taken to safeguard the health of the migrant population

Cu(I)-I-2,4-diaminopyrimidine Coordination Polymers with Optoelectronic Properties as a Proof of Concept for Solar Cells.

Two coordination polymers with formulas [CuI(dapym)]n and [Cu2I2(dapym)]n (dapym = 2,4-diaminopyrimidine) have been synthesized in water at room temperature. According to the stoichiometry used, mono (1D) and the two-dimensional (2D) structures can be obtained. Both are made up of Cu2I2 double chains. Their high insolubility in the reaction medium also makes it possible to obtain them on a nanometric scale. Their structural flexibility and short Cu-Cu distances provoke interesting optoelectronic properties and respond to physical stimuli such as pressure and temperature, making them interesting for sensor applications. The experimental and theoretical studies allow us to propose different emission mechanisms with different behaviors despite containing the same organic ligand. These behaviors are attributed to their structural differences. The emission spectra versus pressure and temperature suggest competencies between different transitions, founding critical Cu2I2 environments, i.e., symmetric in the 1D compound and asymmetric for the 2D one. The intensity in the 2D compound's emission increases with decreasing temperature, and this behavior can be rationalized with a structural constriction that decreases the Cu-Cu and Cu-I distances. However, compound 1D exhibits a contrary behavior that may be related to a change of the organic ligand's molecular configuration. These changes imply that a more significant Π-Π interaction counteracts the contraction in distances and angles when the temperature decreased. Also, the experimental conductivity measurements and theoretical calculations show a semiconductor behavior. The absorption of the 1D compound in UV, its intense emission at room temperature, and the reduction to nanometric size have allowed us to combine it homogeneously with ethyl vinyl acetate (EVA), creating a new composite material. The external quantum efficiency of this material in a Si photovoltaic mini-module has shown that this compound is an active species with application in solar cells since it can move the photons of the incident radiation (UV region) to longer wavelengths.

Structural and Lattice-Dynamical Properties of Tb2O3 under Compression: A Comparative Study with Rare Earth and Related Sesquioxides.

We report a joint experimental and theoretical investigation of the high pressure structural and vibrational properties of terbium sesquioxide (Tb2O3). Powder X-ray diffraction and Raman scattering measurements show that cubic Ia3̅ (C-type) Tb2O3 undergoes two phase transitions up to 25 GPa. We observe a first irreversible reconstructive transition to the monoclinic C2/m (B-type) phase at ∼7 GPa and a subsequent reversible displacive transition from the monoclinic to the trigonal P3̅m1 (A-type) phase at ∼12 GPa. Thus, Tb2O3 is found to follow the well-known C → B → A phase transition sequence found in other cubic rare earth sesquioxides with cations of larger atomic mass than Tb. Our ab initio theoretical calculations predict phase transition pressures and bulk moduli for the three phases in rather good agreement with experimental results. Moreover, Raman-active modes of the three phases have been monitored as a function of pressure, while lattice-dynamics calculations have allowed us to confirm the assignment of the experimental phonon modes in the C- and A-type phases as well as to make a tentative assignment of the symmetry of most vibrational modes in the B-type phase. Finally, we extract the bulk moduli and the Raman-active mode frequencies together with their pressure coefficients for the three phases of Tb2O3. These results are thoroughly compared and discussed in relation to those reported for rare earth and other related sesquioxides as well as with new calculations for selected sesquioxides. It is concluded that the evolution of the volume and bulk modulus of all the three phases of these technologically relevant compounds exhibit a nearly linear trend with respect to the third power of the ionic radii of the cations and that the values of the bulk moduli for the three phases depend on the filling of the f orbitals.

Smart composite films of nanometric thickness based on copper-iodine coordination polymers. Toward sensors.

One-pot reactions between CuI and methyl or methyl 2-amino-isonicotinate give rise to the formation of two coordination polymers (CPs) based on double zig-zag Cu2I2 chains. The presence of a NH2 group in the isonicotinate ligand produces different supramolecular interactions affecting the Cu-Cu distances and symmetry of the Cu2I2 chains. These structural variations significantly modulate their physical properties. Thus, both CPs are semiconductors and also show reversible thermo/mechanoluminescence. X-ray diffraction studies carried out under different temperature and pressure conditions in combination with theoretical calculations have been used to rationalize the multi-stimuli-responsive properties. Importantly, a bottom-up procedure based on fast precipitation leads to nanofibers of both CPs. The dimensions of these nanofibres enable the preparation of thermo/mechanochromic film composites with polyvinylidene difluoride. These films are tens of nanometers in thickness while being centimeters in length, representing smaller thicknesses so far reported for thin-film composites. This nanomaterial integration of CPs could represent a source of alternative nanomaterials for opto-electronic device fabrication.

High pressure luminescence of Nd3+ in YAlO3 perovskite nanocrystals: A crystal-field analysis.

Pressure-induced energy blue- and red-shifts of the 4F3/2 → 4I9/2,11/2 near-infrared emission lines of Nd3+ ions in YAlO3 perovskite nano-particles have been measured from ambient conditions up to 29 GPa. Different positive and negative linear pressure coefficients have been calibrated for the emission lines and related to pressure-induced changes in the interactions between those Nd3+ ions and their twelve oxygen ligands at the yttrium site. Potentiality of the simple overlap model, combined with ab initio structural calculations, in the description of the effects of these interactions on the energy levels and luminescence properties of the optically active Nd3+ ion is emphasized. Simulations show how the energies of the 4f3 ground configuration and the barycenters of the multiplets increase with pressure, whereas the Coulomb interaction between f-electrons decreases and the crystal-field strength increases. All these effects combined explain the wavelength blue-shifts of some near-infrared emission lines of Nd3+ ions. Large pressure rates of various emission lines suggest that a YAlO3 perovskite nano-crystal can be a potential candidate for near-infrared optical pressure sensors.

Experimental and ab Initio Study of Catena(bis(µ2-iodo)-6-methylquinoline-copper(I)) under Pressure: Synthesis, Crystal Structure, Electronic, and Luminescence Properties.

Copper(I) iodine compounds can exhibit interesting mechanochromic and thermochromic luminescent properties with important technological applications. We report the synthesis and structure determination by X-ray diffraction of a new polymeric staircase copper(I) iodine compound catena(bis(µ2-iodo)-6-methylquinoline-copper(I), [C10H9CuIN]. The structure is composed of isolated polymeric staircase chains of copper-iodine coordinated to organic ligands through Cu-N bonds. High pressure X-ray diffraction to 6.45 GPa shows that the material is soft, with a bulk modulus K0 = 10.2(2)GPa and a first derivative K'0 = 8.1(3), typical for organometallic compounds. The unit-cell compression is very anisotropic with the stiffest direction [302] arising from a combination of the stiff CuI ladders and the shear of the planar quinolone ligands over one another. Full structure refinements at elevated pressures show that pressures reduce the Cu···Cu distances in the compound. This effect is detected in luminescence spectra with the appearance of four sub-bands at 515, 600, 647, and 712 nm above 3.5 GPa. Red-shifts are observed, and they are tentatively associated with interactions between copper(I) ions due to the shortening of the Cu···Cu distances induced by pressure, below twice the van der Waals limit (2.8 Å). Additionally, ab initio simulations were performed, and they confirmed the structure and the results obtained experimentally for the equation of state. The simulation allowed the band structure and the electronic density of states of this copper(I) iodine complex to be determined. In particular, the band gap decreases slowly with pressure in a quadratic way with dEg/dP = -0.011 eV/GPa and d(2)Eg/dP(2) = 0.001 eV/GPa(2).

Stokes and anti-Stokes luminescence in Tm(3+)/Yb(3+)-doped Lu3Ga5O12 nano-garnets: a study of multipolar interactions and energy transfer dynamics.

Nanocrystalline Lu3Ga5O12 garnets doped with Tm(3+)/Yb(3+) ions have been synthesized by a low cost and environmentally benign sol-gel technique and characterized for their structural, Stokes and anti-Stokes luminescence properties. The diffuse reflectance spectra of doped Lu3Ga5O12 nano-garnets have been measured to derive the partial energy level structure of Tm(3+) and Yb(3+) ions and possible energy transfer channels between them. Upon laser excitation at 473 nm, weak red and intense near-infrared Stokes emissions have been observed in the nano-garnets. The decay curves of (3)H4 and (1)G4 levels of Tm(3+) ions and the (2)F5/2 level of Yb(3+) ions have been measured upon resonant laser excitation and are found to be non-exponential in nature due to multipolar interactions. In order to know the kind of multipolar interaction among optically active ions, the decay curves are analyzed through the generalized Yokota-Tanimoto model. Moreover, under 970 nm laser excitation, intense blue anti-Stokes emission is observed by the naked eye in Tm(3+)-Yb(3+) co-doped Lu3Ga5O12 nano-garnets. The results show that as-synthesized nano-garnets may be useful in the field of phosphors and photonics.

Structural study of the Eu3+ environments in fluorozirconate glasses: role of the temperature-induced and the pressure-induced phase transition processes in the development of a rare earth's local structure model.

The correlation between the optical properties of the Eu(3+) ions and their local structures in fluorozirconate glasses and glass-ceramics have been analyzed by means of steady-state and time-resolved site-selective laser spectroscopies. Changes in the crystal-field interaction, ranging from weak to medium strength values, are observed monitoring the luminescence and the lifetime of the Eu(3+) ions in different local environments in the glass. As key roles in this study, the Eu(3+) luminescence in the thermally-induced crystallization of the glass and the pressure-induced amorphization of the crystalline phase of the glass-ceramic experimentally states the existence of a parent local structure for the Eu(3+) ions in the glass, identified as the EuZrF(7) crystalline phase. Starting from the ab initio single overlap model, crystal-field calculations have been performed in the glass and the glass-ceramic. From the site-selective measurements, the crystal-field parameters sets are obtained, giving a suitable simulation of the (7)F(J) (J=0-6) Stark energy level diagram for the Eu(3+) ions in the different environments present in the fluorozirconate glass. A simple geometrical model based on a continuous distortion of the parent structure is proposed for the distribution of local environments of the Eu(3+) ions in the fluorozirconate glass.