A review on recent advances in hierarchically porous metal and metal oxide nanostructures as electrode materials for supercapacitors and non-enzymatic glucose sensors

The remarkable significance of electrode materials in industrial processes, energy, sustainability and diabetes monitoring has captivated scientists to develop advance nanomaterials for the benefit of life across the globe. Here in, the recent developments in nanostructured porous metal and metal oxide composite materials for supercapacitor applications and non-enzymatic glucose sensors (NEGS) has been extensively discussed. The essential and active electrode materials from the research and application perspective has been emphasized in detail. We have also evaluated the worthiness, taxonomical classification, efficiency, specific capacitance and sensitivity of these materials for the aforementioned potential applications. Eventually, we concluded the review by providing the aspect ratio, surface morphology, particle size and specific surface area of these materials that plays an indispensable role for their promising potential applications.     

Iron(II) promoted direct synthesis of dibenzo[b,e]oxepin-11(6H)-one derivatives with biological activity. A short synthesis of doxepin

A novel and efficient synthesis of dibenzo[b,e]oxepin-11(6H)-ones by direct intramolecular ortho-acylation from readily available 2-(phenoxymethyl)benzoic acids was developed. The method takes advantage of a newly developed cooperative system consisting of sustainable FeCl₂ and Cl₂CHOCH₃ as the key components. This methodology is compatible with a wide variety of functional groups in good to excellent yields and high regioselectivity. The synthetic application of new protocol was extended to the synthesis of known tricyclic drug doxepin as well as a small library of oxepin based derivatives. For the first time, the obtained dibenzo[b,e]oxepinone derivatives were evaluated for their biological activities on the free-living nematode Caenorhabditis elegans as an effective and cost-efficient model system for anthelmintic discovery.     

Stereospecific Synthesis of Steroidal 20,16-γ-Carbolactones

Two strategies have been explored for the synthesis of steroidal 20,16-γ-carbolactones from the corresponding 17-ketoandrostane. A highly efficient, stereospecific protocol has been developed for the β-oriented cis-γ-lactone, based on a Michael addition of cyanide to a conjugated ketone. A different approach, involving prior attachment of a 3-carbon side chain on C-17 of a 17-oxo-16β-acetoxy-androstane led to the epimeric, α-oriented lactone.     

Electroinitiated Polymerization of 3,3-BIS(N-Carbazolylmethyl)Oxetane

Abstract

3,3-Bis(N-carbazolylmethyl)oxetane, a cyclic compound with carbazolyl substituents closely linked to the oxetane ring, was polymerized by electrochemical initiation in aprotic polar solvents using a quaternary ammonium salt as electrolyte. Colored polymers were obtained as thin films deposited on the anode and were characterized by IR, ¹H NMR, and thermogravimetry. The data obtained refute the classical cationic polymerization of oxetanes.     

Recent developments and comparison of transformation strategies for organic halides to aldehydes and ketones

Molecular Diversity - Aldehydes and ketones are parts of millions of compounds and are important classes of chemicals which serve as important precursors for the synthesis of library of compounds....     

Synthesis of cinnoline 1-oxides by the reaction of ortho-fluoronitrobenzenes with enediamines

Reaction of α-carbonylacetamidines existing in the enediamine tautomeric form with the substituted ortho-fluoronitrobenzene afforded products of the replacement of the fluorine by the α-C atom of amidine. The latter underwent cyclization into cinnoline 1-oxides on treatment with sodium hydride.     

Co-solubilization of the Hydrophobic Drugs Carbamazepine and Nifedipine in Aqueous Nonionic Surfactant Media

Co-solubilization of the hydrophobic drugs Carbamezipine (CBZ) and Nifedipine (NFD) by micellar solutions at 25 °C, using two series of polyoxyethylene based nonionic surfactants, was measured and compared. The first series is composed of surfactants with a 12 carbon (C₁₂) hydrophobic chain while the second series had 16 carbon (C₁₆) hydrophobic chains. Experimental results were obtained for solubilization and co-solubilization of CBZ and NFD within the micelles at saturation and quantification was done in terms of the molar solubilization ratio and the micelle–water partition coefficient employing spectrophotometric and tensiometric techniques. The extent of micellar solubilization of CBZ is much greater than NFD. The C₁₂ series of surfactants exhibit higher solubilization capacities for CBZ than the C₁₆ series while the reverse is the case for NFD. Co-solubilization results showed competitive solubilization of the drugs. A synergistic effect on the solubilization of NFD was observed in the presence of CBZ in Brij30 and Brij56 surfactant systems while, in the remaining surfactants, the solubility of NFD was slightly reduced. Since the surfactants used in the present study are either nontoxic or have minimal toxicity, it is expected that they can be employed as drug delivery vehicles for co-administration of the two drugs in vivo. Both from industrial and research points of view, this paper reports a comprehensive study for co-solubilization of differently structured drugs in micellar media.     

Co‐ and Counterion Effect on the Micellization Characteristics of Dodecylpyridinium Chloride

Micellization parameters, critical micelle concentration (cmc), degree of counterion dissociation (α), aggregation number (n), critical packing parameter, and hydrophobic core volume of Dodecylpyridinium chloride (DPC) micelles were determined in presence of varying concentrations of sodium chloride (NaCl), sodium acetate (SAc), sodium propionate (SPr), ethylammonium chloride (EACl), diethylammonium chloride (DEACl), tetraethylammonium chloride (TEACl), and propylammonium chloride (PACl) through conductometric investigations at 298.15 K. The resulting data suggests that both counter and coions affect the cmc values‐cmc depressing tendency of the salts varies in order PACl≈NaCl>EACl>DEACl>TEACl>SPr>SAc, while the degree of counterion dissociation is dependent on the nature and concentration range of the added salt. Increasing salt concentration increases the relative hydrophobic volume of the micelles and coion has not much effect on aggregation number.     

Fast inputs in the problem of control synthesis under uncertainty

We present a class of bounded control inputs that permits one to solve target control synthesis problems for linear systems with geometric (“instantaneous”) constraints on the perturbations by reduction to simpler programmed control problems.