Synthesis of 2-arylbenzimidazoles and 2-arylbenzothiazoles in both room temperature and microwave condition catalyzed by hexamethylenetetramine-bromine complex

One-pot condensation of 2-aminothiophenol or 1,2-phenylenediamine with different aldehydes has been catalyzed by hexamethylenetetramine-bromine(HMTA-Bromine) as new,available and effective catalyst.2-Arylbenzo thiazoles and 2-aryl benzimidazoles have been achieved in excellent yield and good purity.     

Regioselective bromination and iodination of aromatic substrates promoted by trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane

Selective and efficient bromination and iodination of aromatic compounds by ammonium bromide and ammonium iodide, respectively, under promotion of trans-3,5-dihydroperoxy-3,5-dimethyl-1,2-dioxolane have been explored. Mild reaction conditions, high selectivity and yield, and high reaction rate are some of the major advantages of this synthetic method.     

Application of copper nanoparticles containing natural compounds in the treatment of bacterial and fungal diseases

The development of nanotechnology has generated different nanoscale-sized materials, with metal-based nanomaterials being some of the most interesting and promising. Thousands of articles in various specialized journals all over the world are dedicated to different metallic nanomaterials. Metallic nanomaterials are being widely researched, with gold-, silver-, iron-, and copper-based materials showing potential in medicine. Studies have demonstrated the effect of copper nanoparticles in medicinal herbs on the prevention, control, and treatment of microbial diseases. Experiments have examined the chemical characterization and assessment of the antioxidant, cytotoxicity, antibacterial, and antifungal activities of copper nanoparticles (Cu NPs) using the aqueous extract of Stachys lavandulifolia Vahl flower. These nanoparticles were characterized by UV–visible spectroscopy, field emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectroscopy, transmission electron microscopy (TEM), Fourier-transform infrared spectroscopy (FT-IR), and X-ray diffraction analysis. TEM and FE-SEM images exhibited a uniform spherical morphology and diameters of 10–25 nm for the biosynthesized nanoparticles. FT-IR results suggested polysaccharides and protein in S. lavandulifolia acted as reducing agents, reducing copper ions to Cu NPs. In vitro biological experiments indicated that Cu NPs have excellent antioxidant potential against 2,2-diphenyl-1-picrylhydrazyl, antifungal effects against Candida krusei, Candida parapsilosis, Candida guilliermondii, Candida glabrata, and Candida albicans, and antibacterial activities against Staphylococcus aureus, Enterococcus faecalis, Staphylococcus saprophyticus, Bacillus subtilis, Streptococcus pneumonia, Escherichia coli O157:H7, Salmonella typhimurium, Listeria monocytogenes, Proteus mirabilis, and Pseudomonas aeruginosa. These nanoparticles did not have cytotoxicity properties against human umbilical vein endothelial cells. These results indicate that the inclusion of S. lavandulifolia extract ameliorates the solubility of Cu NPs, which leads to a remarkable enhancement in fungicidal and bactericidal effects under in vitro conditions.     

Shape Memory Hydrogel based on a Hydrophobically‐Modified Polyacrylamide (HMPAM)/α‐CD Mixture via a Host‐Guest Approach

A novel thermally sensitive shape memory (SM) hydrogel is prepared by block copoly­merization of a cationic surfactant monomer, dimethylhexadecyl[2‐(dimethylamino)ethylmethacrylate]ammoniumbromide (C₁₆DMAEMA), and acrylamide (AM) in the presence of α‐cyclodextrin (α‐CD) using N,N’‐methylenebisacrylamide (MBA) as a crosslinker. XRD, solid state ¹³C NMR, and DSC measurements show that the crystalline domains, induced by the hydrogen bonds between α‐CDs threaded on the hydrophobic units of the polymer chains through the host‐guest approach, can reversibly melt and crystallize at different temperatures. Rheological measurements show that both the elastic modulus G’ and viscous modulus G’’ drastically change due to the formation and dissolution of the crystalline domains. These thermo‐sensitive crystalline domains serve as reversible physical crosslinks, endowing the hydrogel with excellent SM properties. Cyclic experiments show that the hydrogel can recover to almost 100% of the deformation in each cycle and can be reused several times.

     

Efficient Synthesis of Urea Derivatives via a Sequential One-Pot Nucleophilic Addition/Ugi Five-Component Reaction Under Solvent-Free Conditions

Urea polyfunctional derivatives were successfully synthesized via a one-pot, five-component nucleophilic addition/Ugi reaction sequence. Simplicity, solvent-free conditions, and good yields of products are advantages of this method.     

Synthesis of gem-Dihydroperoxides from Ketones and Aldehydes Using Silica Sulfuric Acid as Heterogeneous Reusable Catalyst

Silica sulfuric acid (SSA) was found to efficiently catalyze the conversion of aldehydes and ketones directly into the corresponding gem-dihydroperoxides (DHPs) on treatment with aqueous 30% H₂O₂ at room temperature. Mild reaction conditions, good to excellent yields, short reaction times, low environmental impact, and recyclability of the catalyst are the main advantages of this synthetic method.     

Acyl Migration versus Epoxidation in Gold Catalysis: Facile,Switchable, and Atom‐Economic Synthesis of Acylindoles and Quinoline Derivatives

We report a switchable synthesis of acylindoles and quinoline derivatives via gold‐catalyzed annulations of anthranils and ynamides. α‐Imino gold carbenes, generated in situ from anthranils and an N,O‐coordinated gold(III) catalyst, undergo electrophilic attack to the aryl π‐bond, followed by unexpected and highly selective 1,4‐ or 1,3‐acyl migrations to form 6‐acylindoles or 5‐acylindoles. With the (2‐biphenyl)di‐tert‐butylphosphine (JohnPhos) ligand, gold(I) carbenes experienced carbene/carbonyl additions to deliver quinoline oxides. Some of these epoxides are valuable substrates for the preparation of 3‐hydroxylquinolines, quinolin‐3(4H)‐ones, and polycyclic compounds via facile in situ rearrangements. The reaction can be efficiently conducted on a gram scale and the obtained products are valuable substrates for preparing other potentially useful compounds. A computational study explained the unexpected selectivities and the dependency of the reaction pathway on the oxidation state and ligands of gold. With gold(III) the barrier for the formation of the strained oxirane ring is too high; whereas with gold(I) this transition state becomes accessible. Furthermore, energetic barriers to migration of the substituents on the intermediate sigma‐complexes support the observed substitution pattern in the final product.     

Optimum location and influence of tilt angle on performance of solar PV panels

Journal of Thermal Analysis and Calorimetry - With the growing demand of economically feasible, clean, and renewable energy, the use of solar photovoltaic (PV) systems is increasing. The PV panel...