The template efficacy of solid lipid nanoparticles for generating porous silica materials with the amalgamation of Cu‐functionalized cetylpyridinium chloride (CPC; as a co‐emulsifier and as a metal source for generation of CuO oxide nanoparticles) has been explored. Impregnation of CuO nanoparticles (∼10–12 nm) onto the silica matrix proffers to be a propitious route for the fabrication of twin sized porous, highly active catalytic materials. The surface morphology and structural characterization of the synthesized CuO@meso‐macroporous silica framework was elucidated by TEM, field ‐emission (FE)‐SEM, energy‐dispersive X‐ray (EDX), wavelength dispersive (WD)‐XRF, X‐ray photoelectron spectroscopy (XPS), small‐angle X‐ray scattering (SAXS), XRD, and N2 adsorption/desorption studies. All the results have shown that there exists a structural network interconnecting the mesopores with macropores. The catalytic performance of the synthesized framework (ascribed catalyst) was checked for two model reactions. For the reduction of p‐nitrophenol to p‐aminophenol, only 0.25 % (w/v) catalyst was sufficient to accomplish the reaction in 6 min, giving 99.9 % yield. On the other hand, the redox reaction of potassium hexacyanoferrate(III) and sodium thiosulfate utilized 5 % (w/v) catalyst and completed the reaction in 40 min, yielding 98.43 %. Therefore, CuO@meso‐macroporous silica materials could hold great importance in the world of nanocatalysis owing to the present promising results.

For the first time, drying pattern of a sessile droplet of genomic DNA, in the presence of hematite nanoparticles was sighted by polarizing optical microscopy (POM) in this research article. POM results indicated that only at an appreciably high concentration of hematite nanoparticles dried pattern of deoxyribonucleic acid from calf thymus (CT-DNA) was altered. Iron hybridized cetylpyridinium chloride was utilized for the preparation of iron oxide nanoparticles through hydrothermal method. Fourier transforms infrared spectroscopy (FTIR) and powder x-ray diffraction (PXRD) studies confirmed the formation of highly crystalline hematite i.e. α-Fe2O3 nanoparticles. Morphology of the synthesized nanoparticle was visualized by transmission electron microscope (TEM) and field emission scanning electron microscope (FESEM), which revealed that nanoparticles were rhombohedral in shape with a size of 45 ± 10 nm. Based upon all the findings, hydrothermal growth mechanism was also proposed having bilayer protection of surfactant around the nanoparticles. UV-Vis spectroscopy and fluorescence spectroscopy were explored to study the affinity of thus prepared nanoparticles towards calf thymus deoxyribonucleic acid (CT-DNA). The low value of binding constant calculated from the spectroscopy data confirmed the weak interaction between nanoparticles and the CT-DNA.

In the present report, a facile strategy for the synthesis of copper nanoparticles utilizing copper@cetylpyridinium chloride as the metal precursor in combination with vitamin C, was been developed. Synthesized nanoparticles (NPs) were well characterized through UV-Vis spectroscopy, dynamic light scattering (DLS), transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy, energy dispersive X-ray (EDX) spectroscopy, and powder X-ray diffraction (XRD). The as-obtained NPs were used for binding with deoxyribonucleic acid from calf thymus (CT-DNA). Binding potential of synthesized NPs towards DNA was checked by calculating apparent binding constant and various thermodynamic parameters, like ΔG, ΔH, ΔS and number of binding sites from UV-Vis, circular dichroism, and fluorescence spectroscopy. NPs lead to the change in conformation and mobility of the genomic DNA as notify by the circular dichroism and DNA gel electrophoresis. Synergistic effect of synthesized nanoparticles on DNA was also visualized by the tapping mode atomic force microscopy. Research findings of the present work are expected to have an impact on genomic activities.

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