Ligand-Engineered Structural and Physiochemical Properties of 1D Molybdenum-MOFs: A Seldom Explored System for Photocatalytic Applications.

As one of the seldom explored systems, molybdenum-based metal-organic frameworks (Mo-MOFs) with different ligands such as terephthalic acid (Mo-TA), 2-aminoterephthalic acid (Mo-ATA), benzenetricarboxylic acid (Mo-BTC), 2-methylimidazole (Mo-2MI), 2-bipyridine (Mo-2bpy), and 4-bipyridine (Mo-4bpy) were developed in this study. X-ray diffraction (XRD), Raman, and attenuated total reflectance-infrared (ATR-IR) analyses confirmed the ligand-dependent crystal structure of the Mo-MOFs along with the characteristic functional groups present in the respective systems. Interestingly, the morphology of all of these the developed Mo-MOFs was found to be a one-dimensional rod-like structure, which was attributed to the binding nature of the ligands onto the growing Mo-frameworks. Optical analysis indicated that all these Mo-MOFs exhibit ultraviolet (UV) light absorption properties with band gap energy in the range of 3.47-3.03 eV. Among the various Mo-MOFs developed, Mo-4bpy MOF degraded a maximum of ∼76 and 62% of malachite green and Congo red dyes, respectively, under sunlight irradiation. The observed improved photocatalytic efficiency of Mo-4bpy MOF was attributed to its appropriate band edge potential, confirmed by Mott-Schottky analysis, improved carrier lifetime (∼34.6 ns) estimated using the time-resolved photoluminescence (TRPL) spectrum, presence of elements with stable oxidation states in the system confirmed by X-ray photoelectron spectroscopy (XPS), improved charge transfer characteristics, and decreased recombination resistance, as confirmed by impedance and PL analyses, respectively. The degradation of Mo-4bpy MOFs mediated by superoxide (•O2-) and hydroxyl radicals (OH•) was further confirmed by scavenger studies. Cyclic studies performed for up to 5 cycles suggested that the degradation efficiency of the Mo-4bpy MOF was stable, attributed to its excellent structural, optical, and morphological features confirmed via postcharacterization of the recycled photocatalyst.

Anti-bacterial and anti-biofilm properties of green synthesized copper nanoparticles from Cardiospermum halicacabum leaf extract.

In the present study, a copper nanoparticle (Cu NPs) was synthesized by a green synthesis method with Cardiospermum halicacabum leaf extract. The surface area of Cu NPs was measured with dynamic light scattering (DLS). UV-Vis spectrum clearly illustrates the typical absorption peak of Cu NPs. The crystalline property of Cu NPs was confirmed from the XRD pattern. TEM analysis clearly indicates the average particle size of synthesized Cu NPs was in the range of 30-40 nm with hexagonal shape. Energy-dispersive spectroscopy confirms the major strong peaks of Cu NPs. FTIR analysis confirms the existence of various functional biomolecules over the metal nanoparticles and they are playing an important role in the formation of Cu NPs. The antibacterial and anti-biofilm analyses were carried out to confirm their aptitude for biomedical applications. Interestingly, Cu NPs control the development of biofilm by attaching over the cell wall and disturb their growth and development.

Facile one pot synthesis of 2-substituted benzimidazole derivatives under mild conditions by using engineered MgO@DFNS as heterogeneous catalyst.

Benzimidazole derivatives are considered as important heterocyclic motifs that show a wide range of pharmaceutical applications. In view of their wide-ranging bioactivities, it is imperative to direct research on the sustainable catalytic synthesis of benzimidazole. Therefore, herein, we report a novel approach for the synthesis of benzimidazole and its derivatives with engineered MgO supported on dendritic fibrous nano silica (MgO@DFNS) as a sustainable heterogeneous catalyst. The catalyst MgO@DFNS was thoroughly characterized to understand its physio-chemical properties using XRD, FE-SEM, XPS, FT-IR, zeta potential, HR-TEM, TGA, TPR and TPD. The obtained results suggested that the catalyst MgO@DFNS prepared well and have the desired characteristics in it. After the successful characterisation of the prepared catalyst MgO@DFNS, it was applied in the synthesis of benzimidazole derivatives via condensation of o-phenylenediamine, and various aromatic and aliphatic aldehydes under ambient temperature. The catalyst produced a clean reaction profile with excellent yields in a shorter time under the umbrella of green chemistry. The effect of reaction parameters such as the effect of time, catalyst dosage, loading of MgO, effect of solvents and effect of different homo and heterogeneous catalyst were also tested. Furthermore, to understand the scope of the catalyst different substituted diamines and substituted aldehydes were reacted and obtained desired products in good to efficient yield. In addition, a recyclability study was also conducted and it was observed that the catalyst could be recycled for up to six cycles without noticeable changes in the morphology and activity. We believe that the present methodology gave several advantages such as an eco-friendly method, easy work-up, good selectivity, high yields and quick recovery of catalyst. MgO@DFNS is highly stable for several cycles without significant loss of its activity, which possibly demonstrates its applicability at the industrial scale.