An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
A highly efficient fluorosensor based on ultrathin graphitic carbon nitride (g-C₃N₄) nanosheets for Cu(2+) was developed. In the absence of metal ions, the nanosheets exhibit high fluorescence; the strong coordination of the Lewis basic sites on them to metal ions, however, causes fluorescence quenching via photoinduced electron transfer leading to the qualitative and semiquantitative detection of metal ions. This fluorosensor exhibits high selectivity toward Cu(2+). The whole detection process can be completed within 10 min with a detection limit as low as 0.5 nM. The use of test paper enables the naked-eye detection of Cu(2+) with a detection limit of 0.1 nmol. The practical use of this sensor for Cu(2+) determination in real water samples was also demonstrated.
The title compound, C18H22N2O5S, is largely planar, with an r.m.s. deviation of 0.0546 (1) Å of atoms from the mean plane through all non-H atoms except for the methyl groups. The benzene and pyrimidine-dione rings are inclined to one another at a dihedral angle of 1.41 (7)°. In the crystal, weak C-H⋯O inter-actions connect the mol-ecules into chains propagating along the b-axis direction.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
Hydrogen is considered as the "holy grail" for the energy community. One of the most promising strategies to produce hydrogen is to split water using renewable energy such as solar radiation. The abundance of water and solar energy enables the potential of scaling-up of this new technology, if suitable electrocatalysts and solar cells are developed. In this work, a series of materials made of earth-abundant elements was investigated for hydrogen evolution or oxygen evolution reaction. Among the developed catalysts, MoS<sub>2</sub> and NiFe showed the best activities for proton reduction and water oxidation, respectively. These catalysts were further integrated into an alkaline electrolyzer, which delivered a current density of 10 mA cm<sup>-2</sup> at a cell voltage of 1.9 V for water splitting. Using two in-series-connected perovskite solar cells (PSCs) as a power source, a remarkable solar-to-hydrogen conversion efficiency of 12.67 % was achieved in an alkaline electrolyzer with a partial current density of 10.3 mA cm<sup>-2</sup> for hydrogen production. The usage of earth-abundant catalysts in this study, together with the employment of low-cost perovskite light absorber, shows the potential of scaling up this type of photovoltaic electrolyzer for sustainable hydrogen production.
In the title compound, C(11)H(8)N(2)O(2)S, there is a twist in the mol-ecule, with the dihedral angle between the five- and six-membered rings being 31.77 (9)°. The nitro group is slightly twisted out of the plane of the benzene ring to which it is attached [O-N-C-C torsion angle = 9.0 (3)°]. The S and N atoms are syn. In the crystal, supra-molecular layers parallel to (-204) are formed by C-H⋯O and C-H⋯N inter-actions. These layers are connected into a three-dimensional architecture by π-π inter-actions occurring between centrosymmetrically related benzene rings [centroid-centroid distance = 3.6020 (11) Å].
Integrating interdisciplinary healthcare delivery models is essential to improving patient outcomes, enhancing communication among healthcare providers, and optimizing the use of resources. These models emphasize collaboration among healthcare professionals, such as physicians, nurses, social workers, pharmacists, and therapists, to deliver comprehensive care. Communication in these teams is critical, impacting decision-making, care coordination, and patient satisfaction. This review critically analyzes interdisciplinary healthcare delivery models, the challenges related to communication, and the subsequent impact on patient outcomes. The findings suggest that effective communication and team-based care positively influence clinical outcomes, but challenges in coordination and healthcare systems remain barriers to success.
Abstract Compared to homogeneous catalysis, heterogeneous catalysis can achieve product selectivity due to spatial constraints and differences in molecular dimensions of substrates and products by performing the reaction in a confined space. Shape selectivity for substrates, products or transition states is a well‐established phenomenon observed in porous inorganic solids like zeolites with considerable impact in petrochemistry. More recently, metal organic frameworks (MOFs) have emerged as heterogeneous solid catalysts for a broad range of organic reactions due to their unique properties of large surface area, tuneable pore volume and high density of sites. The present mini‐review aims to describe the current evidences showing MOFs as shape‐selective catalysts. After a brief introduction on the concept, types and examples of shape‐selectivity, the available data on MOFs as shape‐selective catalysts have been organized according the nature of active sites promoting the reaction, starting from metal nodes as Lewis acid sites and commenting examples of encapsulated metal nanoparticles (NPs) and molecular guests as centers in various reactions such as addition to carbonyl compounds, hydrogenations, oxidations and oxidative dehydrogenations. The final section provides our view on the current achievements and prospective for future developments in the field.
The title compound, C(14)H(12)N(2)O(2), is almost planar with an r.m.s. deviation for all non-H atoms of 0.038 Å. The observed planarity is rationalized in terms of a close intra-molecular C-H⋯O inter-action. Supra-molecular layers, two mol-ecules thick and with a step topology, are formed in the crystal packing via C-H⋯O contacts involving the carbonyl O atom, which accepts two such bonds, and π-π inter-actions between the components of the fused ring system and the phenyl ring of inversion-related mol-ecules [centroid-centroid distances = 3.6819 (13) and 3.6759 (12) Å].
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
