Enrique Carbó-Argibay

A supramolecular strategy based on molecular dipole moments for high-quality covalent organic frameworks

A supramolecular strategy based on strong molecular dipole moments is presented to gain access to covalent organic framework structures with high crystallinity and porosity. Antiparallel alignment of the molecules within the pore walls is proposed to lead to reinforced columnar stacking, thus affording a high-quality material. As a proof of principle, a novel pyrene dione building block was prepared and reacted with hexahydroxytriphenylene to form a boronic ester-linked covalent organic framework. We anticipate the strategy presented herein to be valuable for producing highly defined COF structures.

Influence of the separation procedure on the properties of magnetic nanoparticles: Gaining in vitro stability and T1–T2 magnetic resonance imaging performance

Ultrasmall superparamagnetic iron oxide nanoparticles (USPIOs) coated with polyacrylic acid (PAA) were synthesized by a hydrothermal method in gram-scale quantity and extensively characterized. Only the nanoparticles subjected to an additional centrifugation step showed narrow size distribution, high polymeric coverage, and ideal superparamagnetism. In addition to improved physico-chemical properties, these nanoparticles feature high stability in vitro as well as dual T1-T2 performance as contrast agents (CAs) for magnetic resonance imaging (MRI), highlighting the importance of the additional separation step in obtaining material with the desired properties.

Up-scaling the synthesis of Cu2O submicron particles with controlled morphologies for solar H2 evolution from water

The synthesis of Cu2O was studied to examine the effects of up-scaling on the size and morphology of the resultant particles. As a result, a successful protocol employing an automated laboratory reactor was developed for large-scale synthesis of phase-pure Cu2O colloids with specific sizes in the submicron to micrometer range (0.2-2.6 μm). The as-synthesized products have been studied by means of powder X-ray diffraction, Raman spectroscopy, X-ray photoelectron spectroscopy, UV-Vis-NIR spectroscopy, scanning electron microscopy, and photoelectrochemical measurements. A broad range of morphologies, both equilibrium (stellated octahedrons, cubes, cuboctahedrons, truncated octahedrons, truncated cuboctahedrons) and metastable (cage-like hierarchical structures, microspheres with flower-like texture), with uniform sizes have been selectively prepared either by careful tuning of synthesis conditions. Recrystallization of primary aggregates through Ostwald ripening is proposed as the formation mechanism for these Cu2O structures. As a photocathode for photoelectrochemical H2 evolution, Cu2O submicron cubes with exposed {001} facets exhibit a high open-circuit potential of ca. 0.9 V vs. the RHE at pH 1.

Magnetite Nanoparticles for Stem Cell Labeling with High Efficiency and Long-Term in Vivo Tracking

Superparamagnetic iron oxide nanoparticles (SPIO-PAA), ultrasmall iron oxide nanoparticles (USPIO-PAA), and glucosamine-modified iron oxide nanoparticles (USPIO-PAA-GlcN) were studied as mesenchymal stem cell (MSCs) labels for cell tracking applications by magnetic resonance imaging (MRI). Pronounced differences were found in the labeling performance of the three samples in terms of cellular dose and labeling efficiency. In combination with polylysine, SPIO-PAA showed nonhomogeneous cell internalization, while for USPIO-PAA no uptake was found. On the contrary, USPIO-PAA-GlcN featured high cellular uptake and biocompatibility, and sensitive detection in both in vitro and in vivo experiments was found by MRI, showing that glucosamine functionalization can be an efficient strategy to increase cell uptake of ultrasmall iron oxide nanoparticles by MSCs.

Straightforward phase-transfer route to colloidal iron oxide nanoparticles for protein immobilization

We report for the first time the effective transfer of hydrophobic oleate-capped iron oxide nanoparticles to an aqueous phase upon treatment with a base bath cleaning solution. We discuss the mechanism of the phase transfer, which involves the elimination of the organic capping agent followed by ionic stabilization of the nanoparticles due to negatively charged Fe–O− surface species. The resultant superparamagnetic aqueous nanocolloid shows excellent protein immobilization capability.

Adsorption of marine phycotoxin okadaic acid on a covalent organic framework

Phycotoxins, compounds produced by some marine microalgal species, can reach high concentrations in the sea when a massive proliferation occurs, the so-called harmful algal bloom. These compounds are especially dangerous to human health when concentrated in the digestive glands of seafood. In order to generate an early warning system to alert for approaching toxic outbreaks, it is very important to improve monitoring methods of phycotoxins in aquatic ecosystems. Solid-phase adsorption toxin tracking devices reported thus far based on polymeric resins have not been able to provide an efficient harmful algal bloom prediction system due to their low adsorption capabilities. In this work, a water-stable covalent organic framework (COF) was evaluated as adsorbent for the hydrophobic toxin okadaic acid, one of the most relevant marine toxins and the parental compound of the most common group of toxins responsible for the diarrhetic shellfish poisoning. Adsorption kinetics of okadaic acid onto the COF in seawater showed that equilibrium concentration was reached in only 60min, with a maximum experimental adsorption of 61mgg-1. Desorption of okadaic acid from the COF was successful with both 70% ethanol and acetonitrile as solvent, and the COF material could be reused with minor losses in adsorption capacity for three cycles. The results demonstrate that COF materials are promising candidates for solid-phase adsorption in water monitoring devices.