Manipulating the Coordination Structure of Molecular Cobalt Sites in Periodic Mesoporous Organosilica for CO Photoreduction.

Photocatalytic CO reduction, including reaction rate, product selectivity, and longevity, is highly sensitive to the coordination structure of the catalytic active sites, and the precise design of the active site remains a challenge in heterogeneous catalysts. Herein, we report on the modulation of the coordination structure of MN -type active sites (M = Co or Ni; = 4 or 5) anchored on a periodic mesoporous organosilica (PMO) support to improve photocatalytic CO reduction. The PMO was functionalized with pendant 3,6-di(2'-pyridyl)pyridazine (dppz) groups to allow immobilization of molecular Co and Ni complexes with polypyridine ligands.

Use of Periodic Mesoporous Organosilica-Benzene Adsorbent for CO Capture to Reduce the Greenhouse Effect.

The CO adsorption of a phenylene-bridged ordered mesoporous organosilica (PMO-benzene) was analyzed. The maximum capture capacity was 638.2 mg·g (0 °C and 34 atm).

Visible-Light-Driven Photocatalytic H Production Using Composites of Co-Al Layered Double Hydroxides and Graphene Derivatives.

The direct conversion of solar energy into chemical energy represents an enormous challenge for current science. One of the commonly proposed photocatalytic systems is composed of a photosensitizer (PS) and a catalyst, together with a sacrificial electron donor (ED) when only the reduction of protons to H is addressed. Layered double hydroxides (LDH) have emerged as effective catalysts.

Iridium-Complexed Dipyridyl-Pyridazine Organosilica as a Catalyst for Water Oxidation.

The heterogenization of metal-complex catalysts to be applied in water oxidation reactions is a currently growing field of great scientific impact for the development of energy conversion devices simulating the natural photosynthesis process. The attachment of IrCp*Cl complexes to the dipyridyl-pyridazine N-chelating sites on the surface of SBA-15 promotes the formation of metal bipyridine-like complexes, which can act as catalytic sites in the oxidation of water to dioxygen, the key half-reaction of artificial photosynthetic systems. The efficiency of the heterogeneous catalyst, Ir@NdppzSBA, in cerium(IV)-driven water oxidation was thoroughly evaluated, achieving high catalytic activity even at a long reaction time.

Solar driven CO reduction with a molecularly engineered periodic mesoporous organosilica containing cobalt phthalocyanine.

A molecular cobalt phthalocyanine (CoPc) catalyst has been integrated in an ethylene-bridged periodic mesoporous organosilica (PMO) to fabricate a hybrid material, CoPc-PMO, that catalyses CO reduction to CO in a photocatalytic system using [Ru(bpy)] (bpy = 2,2'-bipyridine) as a photosensitizer and 1,3-dimethyl-2-phenyl-2,3-dihydro-1-benzo[]imidazole (BIH) as an electron donor. CoPc-PMO displays a Co-based turnover number (TON) of >6000 for CO evolution with >70% CO-selectivity after 4 h irradiation with UV-filtered simulated solar light, and a quantum yield of 1.95% at 467 nm towards CO.

Ru- and Ir-complex decorated periodic mesoporous organosilicas as sensitizers for artificial photosynthesis.

A versatile and facile strategy based on an inverse electron demand Diels-Alder reaction between 5-norbornen-2-yltriethoxysilane and a tetrazine derivative has been established for the synthesis of a new triethoxysilane precursor containing dipyridylpyridazine units. Such a precursor has been incorporated into the mesostructure of an ethylene-bridged periodic mesoporous organosilica (PMO) material through a one-pot synthesis a co-condensation method. Upon attachment of Ru- and Ir-complexes to the pendant N-chelating heterocyclic ligands, the resulting decorated PMOs have acted as photosensitizers in artificial photosynthetic systems.

Efficient Removal of Nonylphenol Isomers from Water by Use of Organo-Hydrotalcites.

The presence of potent organic endocrine-disrupting chemicals (EDCs) in natural aquifers can have adverse impacts on public health and the environment. 4-nonylphenol, one such EDC, can be efficiently removed from water by adsorption onto a clayey material. In this work, we created an effective sorbent for this purpose by using co-precipitation and subsequent ion-exchange to intercalate the organic anion deoxycholate into a Mg/Al hydrotalcite.

Copper-complexed dipyridyl-pyridazine functionalized periodic mesoporous organosilica as a heterogeneous catalyst for styrene epoxidation.

A new heterogeneous catalyst has been synthesized by immobilization of a copper complex on dipyridyl-pyridazine functionalized periodic mesoporous organosilica (dppz-vPMO). This ordered support was first prepared by a co-condensation reaction between vinyltriethoxysilane and 1,2-bis(trimethoxysilyl)ethane and further post-functionalized through a hetero Diels-Alder reaction with 3,6-di-2-pyridyl-1,2,4,5-tetrazine. Techniques such as XRD, N isotherms, TEM, C NMR, XPS and DRIFT, among others, were employed to characterize the surface functionalized materials.

MIL-88A Metal-Organic Framework as a Stable Sulfur-host Cathode for Long-cycle Li-S Batteries.

Lithium-sulfur (Li-S) batteries have received enormous interest as a promising energy storage system to compete against limited, non-renewable, energy sources due to their high energy density, sustainability, and low cost. Among the main challenges of this technology, researchers are concentrating on reducing the well-known "shuttle effect" that generates the loss and corrosion of the active material during cycling. To tackle this issue, metal-organic frameworks (MOF) are considered excellent sulfur host materials to be part of the cathode in Li-S batteries, showing efficient confinement of undesirable polysulfides.

Thiol-Functionalized Ethylene Periodic Mesoporous Organosilica as an Efficient Scavenger for Palladium: Confirming the Homogeneous Character of the Suzuki Reaction.

This work describes the synthesis of thiol-functionalized periodic mesoporous organosilicas (PMOs) prepared using the precursor 1-thiol-1,2-bis(triethoxysilyl)ethane, alone or mixed with 1,2-bis(triethoxysilyl)ethane. The thiol groups incorporated into the structure were found to be efficient for palladium binding. This has allowed these materials to be used as catalysts in the Suzuki cross-coupling reaction of bromobenzene and phenylboronic acid.

Oleate Epoxidation in a Confined Matrix of Hydrotalcite.

Oleate ion was intercalated into a hydrotalcite obtained using a conventional precipitation method and an alternative, novel method involving microwave-assisted ion exchange. The latter method gave a more crystalline hydrotalcite with better textural properties than the former. The spacing between layers in the hydrotalcites was used to epoxidize the double bond in oleate ion.

Identification of pigments in the Annunciation sculptural group (Cordoba, Spain) by micro-Raman spectroscopy.

A highly flexible method based on micro-Raman spectroscopy was used to examine pigment traces on an Annunciation sculpture group dating from the late Middle Ages. The group comprises a statue of the Archangel Gabriel and another of the Virgin Mary. Both are currently housed in the Archaeological Museum of Cordoba, southern Spain.

A Comparative Study of Particle Size Distribution of Graphene Nanosheets Synthesized by an Ultrasound-Assisted Method.

Graphene-based materials are highly interesting in virtue of their excellent chemical, physical and mechanical properties that make them extremely useful as privileged materials in different industrial applications. Sonochemical methods allow the production of low-defect graphene materials, which are preferred for certain uses. Graphene nanosheets (GNS) have been prepared by exfoliation of a commercial micrographite (MG) using an ultrasound probe.

Fast ultrasound-assisted synthesis of highly crystalline MIL-88A particles and their application as ethylene adsorbents.

Highly crystalline MIL-88A particles have been successfully synthesized via fast ultrasound-assisted processes. The influence of the sonication generator and synthesis time on the structure, crystallinity, morphology and surface area of the materials were studied in detail. Under this modified ultrasonic method, X-ray diffraction patterns of MIL-88A particles showed highly crystalline structures in contrast to those reported in literature.

Spectroscopic analysis of corrosion products in a bronze cauldron from the Late Iberian Iron Age.

Selected bronze fragments unearthed at Cerro de la Cruz (Almedinilla, southern Spain) were analyzed to determine the chemical composition of the corrosion products formed on their surface. The fragments came from a large bronze cauldron used in an Iberian village that was devastated in the mid II century BCE - possibly around 141 BCE. The fragments were analyzed by using various instrumental techniques including electron scanning microscopy coupled to energy dispersive X-ray spectroscopy (SEM-EDS), X-ray fluorescence (XRF) spectroscopy, and also by X-ray diffraction (XRD) and micro-Raman spectroscopy.

Luminescent thermometer based on Eu /Tb -organic-functionalized mesoporous silica.

In this work we investigate a mesoporous silica (MS) decorated with dipyridyl-pyridazine (dppz) ligands and further grafted with a mixture of Eu /Tb ions (28.45%:71.55%), which was investigated as a potential thermometer in the 10-360 K temperature range.

Coumarin Derivatives Solvent-Free Synthesis under Microwave Irradiation over Heterogeneous Solid Catalysts.

A suitable methodology of synthesis of coumarin derivatives by Pechmann reaction over heterogeneous solid acid catalysts in a free solvent media under microwave irradiation is described. Resorcinol, phenol and ethyl acetoacetate were selected as model reactants in the Pechmann condensation. The catalytic activity of several materials-Amberlyst-15, zeolite β and sulfonic acid functionalized hybrid silica-in solvent-free microwave-assisted synthesis of the corresponding coumarin derivatives has been investigated in detail.

Thiol-ethylene bridged PMO: A high capacity regenerable mercury adsorbent via intrapore mercury thiolate crystal formation.

Highly ordered thiol-ethylene bridged Periodic Mesoporous Organosilicas were synthesized directly from a homemade thiol-functionalized bis-silane precursor. These high surface area materials contain up to 4.3mmol/g sulfur functions in the walls and can adsorb up to 1183mg/g mercury ions.

Temperature dependent NIR emitting lanthanide-PMO/silica hybrid materials.

Two materials - a mesoporous silica (MS) and a periodic mesoporous organosilica (PMO) functionalized with dipyridyl-pyridazine (dppz) units were grafted with near-infrared (NIR) emitting lanthanide (Nd, Er, Yb) complexes in an attempt to obtain hybrid NIR emitting materials. The parent materials: dppz-vSilica and dppz-ePMO were prepared by a hetero Diels-Alder reaction between 3,6-di(2-pyridyl)-1,2,4,5-tetrazine (dptz) and the double bonds of either ethenylene-bridged PMO (ePMO) or vinyl-silica (vSilica) and subsequent oxidation. The dppz-vSilica is reported here for the first time.

Microwave atmospheric pressure plasma jets for wastewater treatment: Degradation of methylene blue as a model dye.

The degradation of methylene blue in aqueous solution as a model dye using a non thermal microwave (2.45 GHz) plasma jet at atmospheric pressure has been investigated. Argon has been used as feed gas and aqueous solutions with different concentrations of the dye were treated using the effluent from plasma jet in a remote exposure.

Preparation of Palladium-Supported Periodic Mesoporous Organosilicas and their Use as Catalysts in the Suzuki Cross-Coupling Reaction.

Three periodic mesoporous materials, , two organosilicas with either ethylene or phenylene bridges and one silica, have been used as supports for Pd nanoparticles. All Pd-supported samples (1.0 wt%) were prepared by the incipient wetness method and subsequently reduced in an H₂ stream at 200 °C.

100% thiol-functionalized ethylene PMOs prepared by "thiol acid-ene" chemistry.

A novel thiol functionalized bis-silane PMO precursor was synthesized by highly efficient thiol acid-ene chemistry between the double bonds of 1,2-(E)-bis(triethoxysilyl)ethene and thioacetic acid. After aminolysis the self-assembly process of the formed SH-precursor with Pluronic P123 under acidic conditions yields the first 100% thiol-PMO material with good structural ordering.