Studies on the reactions of cyclic oxalyl compounds with hydrazines or hydrazones : Synthesis and reactions of 4‐benzoyl‐1‐(3‐nitrophenyl)‐5‐phenyl‐1H‐pyrazole‐3‐carboxylic acid

The 1H‐pyrazole‐3‐carboxylic acid 2 , obtained from the furan‐2,3‐dione 1 and N‐Benzylidene‐N'‐(3‐nitrophenyl) hydrazine, was converted via reactions of its acid chloride 3 with various alcohols or N‐nucleo‐philes into the corresponding ester or amide derivatives 4 or 5 , respectively. Nitrile 6 and anilino‐pyrazole acid 7 derivatives of 2 were also obtained by dehydration of 5a in a mixture of SOCl₂ with DMF and reduction of 2 with sodium polysulphide, respectively. While cyclocondensation reactions of 2 or 7 with phenyl hydrazine or hydrazine hydrate and 6 with only anhydrous hydrazine lead to derivatives of pyrazolo[3,4‐d]‐pyridazinone 8 and pyrazolo[3,4‐d]pyridazine amine 9 , respectivel. The reaction of 2 with 2‐hydrazinopyri‐dine provided hydrazono‐pyrazole acid derivative 10 , which was decarboxylated to give hydrazono‐pyra‐zole derivative 11 . Pyrazolo[4,3‐d]oxazinone 12 and 2‐quinolyl pyrazolo[3,4‐d]pyridazine 13 derivatives were also prepared by cyclocondensation reactions of 2 with hydroxylamine hydrochloride and 7 with acetaldehyde, respectively.     

Room-temperature phosphorescence of 3- and 5-substituted indoles

The room-temperature phosphorescence of indole and thirteen substituted indoles on Schleicher and Schüll 2040A filter paper is reported. Caesium and iodide ions are effective in increasing the emission intensity. In the presence of iodide, the excitation and emission wavelengths of indole are 279 and 440 nm respectively. The excitation and emission wavelengths of indoles with aliphatic groups in the 3-position are 288-289 and 443-449 nm respectively. Indoles with 3,5-substitution have excitation and emission wavelengths of 300-308 and 448-460 nm respectively. Indoxylsulphate and indoxyl-beta-d-glucoside were the only indoles surveyed for which variations in the excitation and emission wavelengths depended on the heavy-atom ion present. These compounds had excitation wavelengths ranging from 288 to 388 nm, depending on which heavy-atom perturber was used. Emission wavelengths were 460-500 nm. Log-log plots of intensity vs. concentration were linear between 0.05 and 700 microg/ml for all the compounds studied, with detection limits in the nanogram range.     

Complex Compounds of Azomethines with an MN2S2 Five-membered Coordination Unit: Metal Chelates of 2-{[4-(3,5-Diphenyl-4,5-dihydropyrazol-1-yl)benzylidene]amino}benzenethiol

Chelate complexes of 2-{[4-(3,5-diphenyl-4,5-dihydropyrazol-1-yl)benzylidene]amino}benzenethiol (LH) of the ML₂ composition and with an M₂N₂S₂ five-membered coordination unit were obtained. The syntheses were carried out by chemical (from LH and metal acetates) and electrochemical (from LH and zerovalent metals) methods in methanol. The chelate compounds were assigned cis-planar (M = Ni) and tetrahedral (M = Co, Zn, Cd) configurations.     

Synthesis and characterization of polymeric linseed oil grafted methyl methacrylate or styrene

Syntheses of wholly natural polymeric linseed oil (PLO) containing peroxide groups have been reported. Peroxidation, epoxidation and/or perepoxidation reactions of linseed oil, either under air or under oxygen flow at room temperature, resulted in polymeric peroxides, PLO-air and PLO-ofl, containing 1.3 and 3.5 wt.-% of peroxide, with molecular weights of 2 100 and 3 780 Da, respectively. PLO-air contained cross-linked film up to 46.1 wt.-% after a reaction time of 60 d, associated with a waxy, soluble part (PLO-air-s) that was isolated with chloroform extraction. PLO-ofl was obtained as a waxy, viscous liquid without any cross-linked part at the end of 24 d under visible irradiation and oxygen flow. Polymeric peroxides, PLO-air-s and PLO-ofl initiated the free radical polymerization of both methyl methacrylate (MMA) and styrene (S) to give PMMA-graft-PLO and PS-graft-PLO graft copolymers in high yields with Mw varying from 37 to 470 kDa. The polymers obtained were characterized by FT-IR, (1)H NMR, TGA, DSC and GPC techniques. Cross-linked polymers were also studied by means of swelling measurements. PMMA-graft-PLO graft copolymer film samples were also used in cell-culture studies. Fibroblast cells were well adhered and proliferated on the copolymer film surfaces, which is important in tissue engineering.     

A Model for Evaluating and Determining the Most Appropriate Polymer Matrix Type for Natural Fiber Composites

The process of determining the proper polymer matrix type, using a wide range of criteria, to form a natural fiber–reinforced polymer composite is still not established enough. This work introduces, for the first time, a model to select the proper polymer matrix type for natural fibers to enhance the sustainability of the automotive industry. The model was developed to rank different polymers and to determine their relative merits considering 20 different criteria simultaneously, including different physical, mechanical, chemical, environmental, and technical criteria. This work can support establishing a road map for proper selection of polymers in different engineering applications as well as increasing the reliability of the polymer selection process.     

An efficient microwave-assisted synthesis of novel quinolone–triazole and conazole–triazole hybrid derivatives as antimicrobial and anticancer agents

1,2,4-Triazole-fluoroquinolone and 1,2,4-triazole–conazole hybrids are designed, synthesized, and investigated in vitro against a variety of common diseases. The structure of the newly synthesized compounds are characterized from spectral data (IR, ¹H NMR, ¹³C NMR, and LC–MS). The antibacterial activity against both Gram-positive and Gram-negative bacteria is shown to be enhanced by many of the produced compounds. Also, some of the products are found to have strong antiproliferative effects aganist HeLa cervical cancer cells, whilst demonstrating cytotoxic effects toward normal cells.     

Maleic Anhydride Polyethylene Octene Elastomer Toughened Polyamide 6/Polypropylene Nanocomposites: Mechanical and Morphological Properties

A series of polyamide 6/polypropylene (PA6/PP) blends and nanocomposites containing 4 wt% of organophilic modified montmorillonite (MMT) were designed and prepared by melt compounding followed by injection molding. Maleic anhydride polyethylene octene elastomer (POEgMAH) was used as impact modifier as well as compatibilizer in the blend system. Three weight ratios of PA6/PP blends were prepared i.e. 80:20, 70:30, and 60:40. The mechanical properties of PA6/PP blends and nanocomposite were studied through flexural and impact properties. Scanning electron microscopy (SEM) was used to study the microstructure. The incorporation of 10 wt% POEgMAH into PA6/PP blends significantly increased the toughness with a corresponding reduction in strength and stiffness. However, on further addition of 4 wt% organoclay, the strength and modulus increased but with a sacrifice in impact strength. It was also found that the mechanical properties are a function of blend ratio with 70:30 PA6/PP having the highest impact strength, both for blends and nanocomposites. The morphological study revealed that within the blend ratio studied, the higher the PA6 content, the finer were the POEgMAH particles.