Combined Experimental/Theoretical Study on the Luminescent Properties of Homoleptic/Heteroleptic Erbium(III) Anilate-Based 2D Coordination Polymers.

The synthesis, structural and photophysical characterization, and theoretical studies on homo/heteroleptic neutral 2D-layered coordination polymers (CPs), obtained by combining the ErIII ion with chlorocyananilate (ClCNAn) and/or tetrafluoroterephthalate (F4BDC) linkers, are herein reported. The structure of the heteroleptic ErIII-based CP, formulated as [Er2(ClCNAn)2(F4BDC)(DMSO)6]n (1) is also reported. 1 crystallizes in the triclinic P1̅ space group, and the structure consists of neutral 2D layers formed by ErIII ions linked through the two linkers oriented in such a way that the neighboring 2D layers are eclipsed along the a axis, leading to parallelogram-like cavities. Photophysical measurements highlight the prominent role of chlorocyananilate linkers as optical antennas toward lanthanide ions, while wave-function-theory analysis supports the experimental findings, providing evidence for the effect of ligand substitution on the luminescence properties of homo/heteroleptic 2D CPs.

Search for relevant subsets of binary predictors in high dimensional regression for discovering the lead molecule.

One of the main problems that the drug discovery research field confronts is to identify small molecules, modulators of protein function, which are likely to be therapeutically useful. Common practices rely on the screening of vast libraries of small molecules (often 1-2 million molecules) in order to identify a molecule, known as a lead molecule, which specifically inhibits or activates the protein function. To search for the lead molecule, we investigate the molecular structure, which generally consists of an extremely large number of fragments. Presence or absence of particular fragments, or groups of fragments, can strongly affect molecular properties. We study the relationship between molecular properties and its fragment composition by building a regression model, in which predictors, represented by binary variables indicating the presence or absence of fragments, are grouped in subsets and a bi-level penalization term is introduced for the high dimensionality of the problem. We evaluate the performance of this model in two simulation studies, comparing different penalization terms and different clustering techniques to derive the best predictor subsets structure. Both studies are characterized by small sets of data relative to the number of predictors under consideration. From the results of these simulation studies, we show that our approach can generate models able to identify key features and provide accurate predictions. The good performance of these models is then exhibited with real data about the MMP-12 enzyme.

Liquid Phase Synthesis of Nanostructured Spinel Ferrites-A Review.

Nanostructured spinel ferrites with formula M2+Fe2O4 (where M2+ ═ Fe, Co, Mn, Ni, Zn, etc.) represent a class of magnetic materials widely employed in different research fields, due to the possibility of finely tuning the magnetic properties by changing the chemical composition, size, shape, capping agents, etc. Herein, a review of the most common chemical synthesis in liquid media, distinguishing among aqueous and non-aqueous routes, is presented. The experimental procedure together with the mechanism, advantages and disadvantages, and examples are illustrated for each synthetic strategy.

57Fe Mössbauer Spectroscopy for the Study of Nanostructured Mixed Mn-Co Spinel Ferrites.

An oleate-based solvothermal approach has been employed to produce pure CoFe2O4 and MnFe2O4 and mixed Co-Mn ferrites having manganese content in the range 0.13-0.65 and crystallite size of about 8-9 nm. The structural and magnetic properties, studied by powder X-ray diffraction and room temperature 57Fe Mössbauer spectroscopy, have allowed to ascertain the formation of a unique spinel phase in which cobalt and manganese are present and to get insights on the cation distribution and the correlated magnetic properties.

Oleate-Based Solvothermal Approach for Size Control of MIIFe2IIIO4 (MII ═ MnII, FeII) Colloidal Nanoparticles.

The versatility of a promising and repeatable oleate-based solvothermal approach has been explored through the synthesis of MnFe2O4 and λ-Fe2O3/Fe3O4 nanoparticles in form of colloidal dispersions and the tuning of the particle and crystallite sizes. Spinel ferrite nanoparticles with controlled-size in the range 7-14 nm with dispersity below 15% was reached for both MnFe2O4 and λ-Fe2O3/Fe3O4. The size-tuning was obtained with three different pathways: (i) direct approach by changing the solvent polarity or the precursor concentration; (ii) post-synthesis solvothermal treatment in the presence of metal oleates; (iii) post-synthesis solvothermal treatment in the absence of metal oleates.

Raman Spectroscopy as a Probe for Monitoring the Zinc Presence in Zn-Substituted Cobalt Ferrites.

A Raman study on Zinc-substituted Cobalt ferrites, with different Zn(II) contents in each sample of formula: CoFe2O4 (1), Zn0.30Co0.70Fe2.00O4 (2), Zn0.46Co0.54Fe2.02O4 (3), Zn0.53Co0.47Fe2.02O4 (4) is reported. These samples show the same crystallite size (∼6 nm), particle size (∼7 nm) and particle size distribution (∼20%) and they have been synthesized through heating up surfactant-assisted thermal decomposition of metalorganic precursors. The effect of Zn(II) substitution in the cationic distribution is investigated by using the known metal-oxygen vibrational modes in tetrahedral and octahedral sites. The presence of Zn(II) metal ion is determined through the band at 150 cm-1 (T2g(1) phonon mode), which is not present in the pure Co-ferrite, a blue-shift of the Eg vibrational mode depending on Zn(II)/Co(II) cationic distribution and a shoulder at ∼250 cm-1, which appears when zinc enters in the structure, and a broadening and a red-shift in the A1g phonon mode is observed in Raman spectra of 2-4 samples. Interestingly the latter represents a potential key probe to monitor the Zn(II) presence in Zn-substituted Co-ferrites.

Insights into NdIII to YbIII Energy Transfer and Its Implications in Luminescence Thermometry.

This work challenges the conventional approach of using NdIII 4F3/2 lifetime changes for evaluating the experimental NdIII → YbIII energy transfer rate and efficiency. Using near-infrared (NIR) emitting Nd:Yb mixed-metal coordination polymers (CPs), synthesized via solvent-free thermal grinding, we demonstrate that the NdIII [2H11/2 → 4I15/2] → YbIII [2F7/2 → 2F5/2] pathway, previously overlooked, dominates energy transfer due to superior energy resonance and J-level selection rule compatibility. This finding upends the conventional focus on the NdIII [4F3/2 → 4I11/2] → YbIII [2F7/2 → 2F5/2] transition pathway. We characterized Nd0.890Yb0.110(BTC)(H2O)6 as a promising cryogenic NIR thermometry system and employed our novel energy transfer understanding to perform simulations, yielding theoretical thermometric parameters and sensitivities for diverse Nd:Yb ratios. Strikingly, experimental thermometric data closely matched the theoretical predictions, validating our revised model. This novel perspective on NdIII → YbIII energy transfer holds general applicability for the NdIII/YbIII pair, unveiling an important spectroscopic feature with broad implications for energy transfer-driven materials design.

Hard-Soft Core-Shell Architecture Formation from Cubic Cobalt Ferrite Nanoparticles.

Cubic bi-magnetic hard-soft core-shell nanoarchitectures were prepared starting from cobalt ferrite nanoparticles, prevalently with cubic shape, as seeds to grow a manganese ferrite shell. The combined use of direct (nanoscale chemical mapping via STEM-EDX) and indirect (DC magnetometry) tools was adopted to verify the formation of the heterostructures at the nanoscale and bulk level, respectively. The results showed the obtainment of core-shell NPs (CoFe2O4@MnFe2O4) with a thin shell (heterogenous nucleation). In addition, manganese ferrite was found to homogeneously nucleate to form a secondary nanoparticle population (homogenous nucleation). This study shed light on the competitive formation mechanism of homogenous and heterogenous nucleation, suggesting the existence of a critical size, beyond which, phase separation occurs and seeds are no longer available in the reaction medium for heterogenous nucleation. These findings may allow one to tailor the synthesis process in order to achieve better control of the materials' features affecting the magnetic behaviour, and consequently, the performances as heat mediators or components for data storage devices.

Intra-source provenance study on Monte Arci (Sardinia) obsidian by pXRF: Role of the data acquisition and analysis tools.

In this work, a detailed study of Monte Arci obsidian sub-sources using the increasingly accessible technique of pXRF is presented based upon a large dataset of 68 geological samples, for the development of X-ray fluorescence-based analytical standardless procedure. In addition, a non-conventional (for obsidian provenance study) direct application of multivariate analysis on XRF spectra (continuous variables), rather than absolute concentrations or intensity ratios (discrete variables) is proposed. Results from different softwares and data analysis approaches (bi-/trivariate versus multivariate) were compared. In a blind test, the bi-/trivariate approach led to the correct assignment for the main SA, SB, and SC sub-sources, taking into account averaged values of intensity ratios with their standard deviation obtained from three independent measurements. A high intra-source variability for the SB subgroups was detected (almost 13% of error in the assignment, 9 samples out of 68). A non-conventional application of multivariate analysis was carried out directly on the XRF spectra and correct assignments were obtained for SA, SB1, SC groups, while 71% of the SB2 samples were correctly identified. The non-destructive analysis on 14 archaeological samples from Su Carroppu (Carbonia, southwestern Sardinia) rockshelter and from the Middle Neolithic (MN) 422 structure of the open-air dwelling site at Cuccuru is Arrius (Cabras, central-western Sardinia) permitted to test the method and hypothesise their provenance. The comparison with visual characterization or previous analyses by Particle Induced X-Ray Emission (PIXE) permitted to verify the correct provenance assignment of all artifacts for the bi-/trivariate method, and for 12/14 samples in the case of the multivariate one. The standardless analytical approach proposed in this work can represent a more general method exploitable for other obsidian sources, other glassy materials, besides other materials of archaeological interest.

Size dependence of the surface spin disorder and surface anisotropy constant in ferrite nanoparticles.

The magnetic properties of nanoscale magnets are greatly influenced by surface anisotropy. So far, its quantification is based on the examination of the blocking temperature shift within a series of nanoparticles of varying sizes. In this scenario, the surface anisotropy is assumed to be a particle size-independent quantity. However, there is no solid experimental proof to support this simplified picture. On the contrary, our work unravels the size-dependent magnetic morphology and surface anisotropy in highly uniform magnetic nanoparticles using small-angle polarized neutron scattering. We observed that the surface anisotropy constant does not depend on the nanoparticle's size in the range of 3-9 nm. Furthermore, our results demonstrate that the surface spins are less prone to polarization with increasing nanoparticle size. Our study thus proves the size dependence of the surface spin disorder and the surface anisotropy constant in fine nanomagnets. These findings open new routes in materials based on a controlled surface spin disorder, which is essential for future applications of nanomagnets in biomedicine and magnonics.

Effect of different molecular coatings on the heating properties of maghemite nanoparticles.

In this work, the effect of different molecular coatings on the alternating magnetic field-induced heating properties of 15 nm maghemite nanoparticles (NPs) in water dispersions was studied at different frequencies (159-782 kHz) and field amplitudes (100-400 G). The original hydrophobic oleate coating was replaced with dimercaptosuccinic acid (DMSA) or polyethylene glycol trimethoxysilane (PEGTMS), while cetrimonium bromide (CTAB) or stearic acid-poloxamer 188 (SA-P188) was intercalated or encapsulated, respectively, to transfer the dispersions into water. Surface modification, based on intercalation processes, induced clustering phenomena with the formation of spherical-like assemblies (CTAB and SA-P188), while ligand-exchange strategies kept the particles isolated. The clustering phenomenon has detrimental effects on the heating performances compared with isolated systems, in line with the reduction of Brown relaxation times. Furthermore, broader comprehension of the heating phenomenon in this dynamic system is obtained by following the evolution of SPA and ILP with time and temperature beyond the initial stage.

Germination and early seedling development of Helichrysum microphyllum Cambess. subsp. tyrrhenicum Bacch., Brullo & Giusso in the presence of arsenates and arsenites.

Arsenate, As(V), and arsenite, As(III), are the most available arsenicals present in the soil solutions, in particular in mine polluted substrates, and cause several symptoms of toxicity in plants (like inhibition of seed germination and reduction of seedling development). For these reasons, seeds germination studies are essential for the design of phytoremediation activities of mine sites. Seed germination and seedling development of Helichrysum microphyllum subsp. tyrrhenicum, were evaluated at 15 °C using various concentrations of As(V) and As(III) (0-500 mg/L and 0-200 mg/L, respectively). Seeds were harvested (I) into a mine dump contaminated in As, (II) nearby this site, and (III) faraway the As contaminated area and without mine activities. Seed germination, cotyledons emergence, and seedling mortality were evaluated for 90 days. As(V) and As(III) acted differently, showing a much higher toxicity when arsenite was added than arsenate. The taxon was able to germinate, develop cotyledons, and survive under all arsenate concentrations, whereas arsenite acted on these steps already at 2.5 mg/L. Moreover, a linear decrease in cotyledons emergence was assessed with the increase of both arsenicals' concentrations, as well as a linear decrease of seedling survival under arsenite. The taxon showed great adaptability to As pollution, giving an important contribution in phytoremediation of mining sites.

As(III, V) Uptake from Nanostructured Iron Oxides and Oxyhydroxides: The Complex Interplay between Sorbent Surface Chemistry and Arsenic Equilibria.

Iron oxides/oxyhydroxides, namely maghemite, iron oxide-silica composite, akaganeite, and ferrihydrite, are studied for AsV and AsIII removal from water in the pH range 2-8. All sorbents were characterized for their structural, morphological, textural, and surface charge properties. The same experimental conditions for the batch tests permitted a direct comparison among the sorbents, particularly between the oxyhydroxides, known to be among the most promising As-removers but hardly compared in the literature. The tests revealed akaganeite to perform better in the whole pH range for AsV (max 89 mg g-1 at pH0 3) but to be also efficient toward AsIII (max 91 mg g-1 at pH0 3-8), for which the best sorbent was ferrihydrite (max 144 mg g-1 at pH0 8). Moreover, the study of the sorbents' surface chemistry under contact with arsenic and arsenic-free solutions allowed the understanding of its role in the arsenic uptake through electrophoretic light scattering and pH measurements. Indeed, the sorbent's ability to modify the starting pH was a crucial step in determining the removal of performances. The AsV initial concentration, contact time, ionic strength, and presence of competitors were also studied for akaganeite, the most promising remover, at pH0 3 and 8 to deepen the uptake mechanism.

Technological insights on the Early-Middle Bronze Age pottery of Monte Meana cave (Sardinia, Italy).

An important Bronze Age settlement was discovered during an archaeological excavation in the Monte Meana karst cave in south-western Sardinia (Italy) between 2007 and 2012. In this region, the caves were used since the Neolithic for different purposes, such as burials or other rituals. The dig highlighted a rare example of domestic use of a cave and showed a case study of household space of the Early -Middle Bronze Age, at the beginning of the Nuragic civilization. This provided the opportunity to investigate through a multidisciplinary approach, the empirical knowledge of ancient potters and technological characters of local pottery production especially in relation to domestic use, in a context at that time devoid of external cultural interferences. For this purpose, a selection of 24 pottery sherds related to vessel forms for cooking, storage, and eating were studied through macroscopic surveys and archaeometric analysis by petrography, scanning electron microscopy, X-ray powder diffraction, and Fourier transform infrared spectroscopy. The results revealed some discriminant variables (shape, wall thickness, features of the paste, surface smoothing, presence of diagnostic mineralogical phases, and tempers), within the ceramic products of this Sardinian Bronze Age site, showing skillful management of firing temperatures.

The Boundary Between Volume and Surface-Driven Magnetic Properties in Spinel Iron Oxide Nanoparticles.

Despite modern preparation techniques offer the opportunity to tailor the composition, size, and shape of magnetic nanoparticles, understanding and hence controlling the magnetic properties of such entities remains a challenging task, due to the complex interplay between the volume-related properties and the phenomena occurring at the particle's surface. The present work investigates spinel iron oxide nanoparticles as a model system to quantitatively analyze the crossover between the bulk and the surface-dominated magnetic regimes. The magnetic properties of ensembles of nanoparticles with an average size in the range of 5-13 nm are compared. The role of surface anisotropy and the effect of oleic acid, one of the most common and versatile organic coatings, are discussed. The structural and morphological properties are investigated by X-ray diffraction and transmission electron microscopy. The size dependence of the surface contribution to the effective particle anisotropy and the magnetic structure are analyzed by magnetization measurements and in-field Mössbauer spectrometry. The structural data combined with magnetometry and Mössbauer spectrometry analysis are used to shed light on this complex scenario revealing a crossover between volume and surface-driven properties in the range of 5-7 nm.

On the synthesis of bi-magnetic manganese ferrite-based core-shell nanoparticles.

Multifunctional nano-heterostructures (NHSs) with controlled morphology are cardinal in many applications, but the understanding of the nanoscale colloidal chemistry is yet to be fulfilled. The stability of the involved crystalline phases in different solvents at mid- and high-temperatures and reaction kinetics considerably affect the nucleation and growth of the materials and their final architecture. The formation mechanism of manganese ferrite-based core-shell NHSs is herein investigated. The effects of the core size (8, 10, and 11 nm), the shell nature (cobalt ferrite and spinel iron oxide) and the polarity of the solvent (toluene and octanol) on the dissolution phenomena of manganese ferrite are also studied. Noteworthily, the combined use of bulk (powder X-ray diffraction, 57Fe Mössbauer spectroscopy, and DC magnetometry) and nanoscale techniques (HRTEM and STEM-EDX) provides new insights into the manganese ferrite dissolution phenomena, the colloidal stability in an organic environment, and the critical size below which dissolution is complete. Moreover, the dissolved manganese and iron ions react further, leading to an inverted core-shell in the mother liquor solution, paving the way to novel synthetic pathways in nanocrystal design. The MnFe2O4@CoFe2O4 core-shell heterostructures were also employed as heat mediators, exploiting the magnetic coupling between a hard (CoFe2O4) and a soft phase (MnFe2O4).

Meso- and macroporous silica-based arsenic adsorbents: effect of pore size, nature of the active phase, and silicon release.

Arsenic pollution in ground and drinking water is a major problem worldwide due to the natural abundance of arsenic by dissolution from ground sediment or mining activities from anthropogenic activities. To overcome this issue, iron oxides as low-cost and non-toxic materials, have been widely studied as efficient adsorbents for arsenic removal, including when dispersed within porous silica supports. In this study, two head-to-head comparisons were developed to highlight the As(v)-adsorptive ability of meso- and macrostructured silica-based adsorbents. First, the role of the textural properties of a meso-(SBA15) and macrostructured (MOSF) silica support in affecting the structural-morphological features and the adsorption capacity of the active phase (Fe2O3) have been studied. Secondly, a comparison of the arsenic removal ability of inorganic (Fe2O3) and organic (amino groups) active phases was carried out on SBA15. Finally, since silica supports are commonly proposed for both environmental and biomedical applications as active phase carriers, we have investigated secondary silicon and iron pollution. The batch tests at different pH revealed better performance from both Fe2O3-composites at pH 3. The values of q m of 7.9 mg g-1 (53 mg gact -1) and 5.5 mg g-1 (37 mg gact -1) were obtained for SBA15 and MOSF, respectively (gact stands for mass of the active phase). The results suggest that mesostructured materials are more suitable for dispersing active phases as adsorbents for water treatment, due to the obtainment of very small Fe2O3 NPs (about 5 nm). Besides studying the influence of the pore size of SBA15 and MOSF on the adsorption process, the impact of the functionalization was analyzed on SBA15 as the most promising sample for As(v)-removal. The amino-functionalized SBA15 adsorbent (3-aminopropyltriethoxysilane, APTES) exhibited a q m of 12.4 mg g-1 and faster kinetics. Furthermore, issues associated with the release of iron and silicon during the sorption process, causing secondary pollution, were evaluated and critically discussed.

Self-Limitations of Heat Release in Coupled Core-Shell Spinel Ferrite Nanoparticles: Frequency, Time, and Temperature Dependencies.

We explored a series of highly uniform magnetic nanoparticles (MNPs) with a core-shell nanoarchitecture prepared by an efficient solvothermal approach. In our study, we focused on the water dispersion of MNPs based on two different CoFe2O4 core sizes and the chemical nature of the shell (MnFe2O4 and spinel iron oxide). We performed an uncommon systematic investigation of the time and temperature evolution of the adiabatic heat release at different frequencies of the alternating magnetic field (AMF). Our systematic study elucidates the nontrivial variations in the heating efficiency of core-shell MNPs concerning their structural, magnetic, and morphological properties. In addition, we identified anomalies in the temperature and frequency dependencies of the specific power absorption (SPA). We conclude that after the initial heating phase, the heat release is governed by the competition of the Brown and Néel mechanism. In addition, we demonstrated that a rational parameter sufficiently mirroring the heating ability is the mean magnetic moment per MNP. Our study, thus, paves the road to fine control of the AMF-induced heating by MNPs with fine-tuned structural, chemical, and magnetic parameters. Importantly, we claim that the nontrivial variations of the SPA with the temperature must be considered, e.g., in the emerging concept of MF-assisted catalysis, where the temperature profile influences the undergoing chemical reactions.

Nanoscaled Metal-Organic Frameworks: Challenges Towards Biomedical Applications.

Achieving metal-organic frameworks (MOFs) in the form of nanoparticles (NanoMOFs) represents a recent challenge due to the possibility to combine the intrinsic porosity of these materials with the nanometric dimension, a fundamental requirement for strategic biomedical applications. In this outlook we envision the current/future opportunities of the NanoMOFs in the field of biomedicine, with particular emphasis on (i) biocompatible MOFs composition; (ii) MOFs miniaturization and (iii) nanoMOFs applications.