Exploring metal carbamates as precursors for the synthesis of metal-organic frameworks.

In the synthesis of metal-organic frameworks (MOFs), the choice of the metal precursor plays a key role because of the influence that it can exert on the crystallization kinetics. The present work explores the use of metal-carbamato complexes for the synthesis of benchmark MOFs, namely HKUST-1 and UiO-66. Cu(OCNEt)·2NHEt and Zr(OCNEt), prepared using straightforward CO fixation reactions starting from the corresponding metal chlorides and diethylamine, were employed as metal precursors for MOF formation.

"Activated Borane": A Porous Borane Cluster Polymer as an Efficient Lewis Acid-Based Catalyst.

Borane cluster-based porous covalent networks, named activated borane (), were prepared by cothermolysis of decaborane(14) (-BH) and selected hydrocarbons (toluene, cyclohexane, ; and -hexane, ) under anaerobic conditions. These amorphous solid powders exhibit different textural and Lewis acid (LA) properties that vary depending on the nature of the constituent organic linker. For , its LA strength even approaches that of the commonly used molecular LA, B(CF).

Simple method for quantification of metal-based particles in biopsy samples of patients with long bone implants - Pilot study.

The presence of particles fixed in tissue samples due to implant degradation or disintegration plays an important role in post-operative complications. The ability to determine the size, shape, chemical composition and, above all, the number of these particles can be used in many areas of medicine. This study presents a novel, simple metal-based particle detection method using scanning electron microscopy with energy dispersive spectrometer (SEM-EDS).

Linker-Functionalized Phosphinate Metal-Organic Frameworks: Adsorbents for the Removal of Emerging Pollutants.

Metal-organic frameworks (MOFs) are attracting increasing attention as adsorbents of contaminants of emerging concern that are difficult to remove by conventional processes. This paper examines how functional groups covering the pore walls of phosphinate-based MOFs affect the adsorption of specific pharmaceutical pollutants (diclofenac, cephalexin, and sulfamethoxazole) and their hydrolytic stability. New structures, isoreticular to the phosphinate MOF ICR-7, are presented.

Water-based synthesis and nitrate release properties of a Zr-based metal-organic framework derived from L-aspartic acid.

We report the synthesis and characterisation of a cationic metal-organic framework (MOF) based on Zr and L-aspartate and containing nitrate as an extra framework counteranion, named MIP-202-NO. The ion exchange properties of MIP-202-NO were preliminarily investigated to evaluate its potential as a platform for controlled release of nitrate, finding that it readily releases nitrate in aqueous solution.

5th Metatarsal Jones Fracture - To Treat Conservatively, or Surgically Using Headless Double-Threaded Herbert Screw?

PURPOSE OF THE STUDY Fifth metatarsal fractures, in particular so-called Jones fractures, are relatively common injuries both in the general population and athletes. Although discussions about whether the surgical or conservative solution should be preferred are ongoing for decades, there is no clear consensus. Here, we aimed to prospectively compare the results of osteosynthesis using the Herbert screw with the conservative solution in patients from our department.

Exploring the Isoreticular Continuum between Phosphonate- and Phosphinate-Based Metal-Organic Frameworks.

The rational design of metal-organic frameworks (MOFs) is one of the driving forces behind the great success that this class of materials is experiencing. The so-called isoreticular approach is a key design tool, very often used to tune the size, steric properties, and additional functional groups of the linker used. In this work, we go one step further and show that even linkers with two different coordinating groups, namely, phosphonate and phosphinate, can form isoreticular MOFs.

Review of ankle rehabilitation devices for treatment of equinus contracture.

Introduction: Equinus contracture is a serious disability and attention should be paid to proper and effective treatment. Most attention is given to neurologically impaired patients, but the incidence of equinus contracture is much higher, for example, in post-traumatic patients. In addition to conventional physical therapy, robotic rehabilitation treatment is one of the promising procedures to precede severe contraction cases and the need for surgery.

"Activated Borane" - A Porous Borane Cluster Network as an Effective Adsorbent for Removing Organic Pollutants.

The unprecedented co-thermolysis of decaborane(14) (nido-B H ) and toluene results in a novel porous material (that we have named "activated borane") containing micropores between 1.0 and 1.5 nm in diameter and a specific surface area of 774 m  g (Ar, 87 K) that is thermally stable up to 1000 °C.

Phosphinate MOFs Formed from Tetratopic Ligands as Proton-Conductive Materials.

Metal-organic frameworks (MOFs) are attracting attention as potential proton conductors. There are two main advantages of MOFs in this application: the possibility of rational design and tuning of the properties and clear conduction pathways given by their crystalline structure. We hereby present two new MOF structures, ICR-10 and ICR-11, based on tetratopic phosphinate ligands.

Tension Hemothorax in Aortic Rupture: A Case Report.

The standard ATLS protocol calls for chest drain insertion in patients with hemothorax before performing further diagnostic steps. However, if trauma-induced thoracic aortic rupture is the underlying cause, such drainage can lead to massive bleeding and death of the patient. This report describes a case of a polytrauma patient (car accident), aged 21, with symmetrical chest and decreased breath sounds dorsally on the left.

Robust Aluminum and Iron Phosphinate Metal-Organic Frameworks for Efficient Removal of Bisphenol A.

Porous metal-organic frameworks (MOFs) have excellent characteristics for the adsorptive removal of environmental pollutants. Herein, we introduce a new series of highly stable MOFs constructed using Fe and Al metal ions and bisphosphinate linkers. The isoreticular design leads to ICR-2, ICR-6, and ICR-7 MOFs with a honeycomb arrangement of linear pores, surface areas up to 1360 m g, and high solvothermal stabilities.

Phosphinate Apical Ligands: A Route to a Water-Stable Octahedral Molybdenum Cluster Complex.

Recent studies have unraveled the potential of octahedral molybdenum cluster complexes (Mo) as relevant red phosphors and photosensitizers of singlet oxygen, O(Δ), for photobiological applications. However, these complexes tend to hydrolyze in an aqueous environment, which deteriorates their properties and limits their applications. To address this issue, we show that phenylphosphinates are extraordinary apical ligands for the construction of Mo complexes.

The nanoscaled metal-organic framework ICR-2 as a carrier of porphyrins for photodynamic therapy.

Nanosized porphyrin-containing metal-organic frameworks (MOFs) attract considerable attention as solid-state photosensitizers for biological applications. In this study, we have for the first time synthesised and characterised phosphinate-based MOF nanoparticles, nanoICR-2 (Inorganic Chemistry Rez). We demonstrate that nanoICR-2 can be decorated with anionic 5,10,15,20-tetrakis(4-R-phosphinatophenyl)porphyrins (R = methyl, isopropyl, phenyl) by utilizing unsaturated metal sites on the nanoparticle surface.

Zirconium Metal-Organic Framework UiO-66: Stability in an Aqueous Environment and Its Relevance for Organophosphate Degradation.

Zirconium-based metal-organic frameworks were recently investigated as catalysts for degradation of organophosphate toxic compounds, such as pesticides or chemical warfare agents. The most utilized UiO-66 is considered as a stable material for these applications in an aqueous environment. However, the presented results indicate that the properties of UiO-66 are changing considerably in aqueous media under common conditions used for organophosphate degradations, and therefore its catalytic activity is not related to the number of structural defects created during the material synthesis.

Phosphinatophenylporphyrins tailored for high photodynamic efficacy.

The development of effective photosensitizers is particularly attractive for photodynamic therapy of cancer. Three novel porphyrin photosensitizers functionalized with phosphinic groups were synthesized and their physicochemical, photophysical, and photobiological properties were collected. Phosphinic acid groups (R1R2POOH) attached to the porphyrin moiety (R1) contain different R2 substituents (methyl, isopropyl, phenyl in this study).

Designing Porphyrinic Covalent Organic Frameworks for the Photodynamic Inactivation of Bacteria.

Microbial colonization of biomedical devices is a recognized complication contributing to healthcare-associated infections. One of the possible approaches to prevent surfaces from the biofilm formation is antimicrobial photodynamic inactivation based on the cytotoxic effect of singlet oxygen, O(Δ), a short-lived, highly oxidative species, produced by energy transfer between excited photosensitizers and molecular oxygen. We synthesized porphyrin-based covalent organic frameworks (COFs) by Schiff-base chemistry.

Phosphinic Acid Based Linkers: Building Blocks in Metal-Organic Framework Chemistry.

Metal-organic frameworks (MOFs) are a chemically and topologically diverse family of materials composed of inorganic nodes and organic linkers bound together by coordination bonds. Presented here are two significant innovations in this field. The first is the use of a new coordination group, phenylene-1,4-bis(methylphosphinic acid) (PBPA), a phosphinic acid analogue of the commonly used terephtalic acid.

Postsynthetic modification of a zirconium metal-organic framework at the inorganic secondary building unit with diphenylphosphinic acid for increased photosensitizing properties and stability.

A zirconium metal-organic framework (MOF) PCN-222 was postsynthetically modified with diphenylphosphinic acid, resulting in an increased stability when activated from water and 4 times higher photosensitizing properties for singlet oxygen production. The phosphinic acid did not compromise the crystallinity of the MOF but made strong bonds with the zirconia secondary building units.

Nickel-cobalt hydroxide nanosheets: Synthesis, morphology and electrochemical properties.

This paper reports the synthesis, characterization, and electrochemical performance of nickel-cobalt hydroxide nanosheets. The hydroxide nanosheets of approximately 0.7nm thickness were prepared by delamination of layered nickel-cobalt hydroxide lactate in water and formed transparent colloids that were stable for months.

Nanoscaled porphyrinic metal-organic frameworks: photosensitizer delivery systems for photodynamic therapy.

The photocytotoxic activity of porphyrin-containing materials including metal-organic frameworks (MOFs) has attracted ever increasing interest. We have developed a simple synthesis of hexagonal PCN-222/MOF-545 nanoparticles, which are powerful in inducing reactive oxygen species-mediated apoptosis of cancer cells upon visible light irradiation. The extent of the cytotoxic effect well correlates with the nanoparticle size and structural instability.

Combined bone lesion analysis in 3D CT data of vertebrae.

Two novel statistically based methods for bone lesion detection and classification are presented. Together with the previously published MRF method [15], they form a triad of mutually complementary methods that promise, when fused, to enable higher reliability of bone lesion assessment.

Facile synthesis of CuO nanosheets via the controlled delamination of layered copper hydroxide acetate.

CuO nanosheets were prepared by the controlled delamination of layered copper hydroxide acetate followed by the in situ solvothermal transformation of hydroxide to oxide. The reaction was performed in 1-butanol in order to prevent recrystallization or nanoparticle aggregation. Analyses by small angle X-ray scattering, transmission electron microscopy, and atomic force microscopy revealed that the CuO nanosheets are approximately 1 nm thin, corresponding to three to four stacked CuO6 octahedral layers.