On Lattice Representations with Dcc Posets

Order - In this paper, we investigate the class of lattices representable with posets satisfying the DCC condition. We describe a way to decide whether a finite lattice is in this class. We also...     

Chemoselective Suzuki–Miyaura reactions of 4-trifluoromethylsulfonyloxy-6-bromocoumarin

Suzuki–Miyaura reactions of 4-trifluoromethylsulfonyloxy-6-bromocoumarin provide a convenient access to arylated coumarins. The reactions proceed with excellent chemoselectivity in favour of position 4.     

Cyclodextrin complexation improves aqueous solubility of the antiepileptic drug,rufinamide: solution and solid state characterization of compound-cyclodextrin binary systems

Rufinamide (RUF) was characterized in terms of cyclodextrin (CD) complexation in order to improve its aqueous solubility. Binary systems of RUF with three CDs—β-cyclodextrin (β-CD), randomly methylated-β-cyclodextrin (RAMEB) and sulfobutylether-β-cyclodextrin (SBE-β-CD)—were characterized with a wide variety of analytical techniques. Liquid state characterization was carried out by complementary techniques such as nuclear magnetic resonance spectroscopy (NMR), capillary electrophoresis (CE), mass spectrometry (MS) and phase solubility studies. The latter revealed that the stability of the complexes decreased in the order of RAMEB?>?β-CD?>?SBE-β-CD. A_L-type diagrams were obtained in all cases, characteristic of 1:1 stoichiometry, with a maximum of over 15-fold increase in RUF solubility, when complexed with RAMEB. NMR Job plot and MS studies confirmed phase solubility results, regarding the binding stoichiometry. ¹H NMR and 2D ROESY investigations revealed the inclusion of the triazole moiety of RUF, confirmed by molecular modeling. Solid state complexation in 1:1 molar ratio was carried out by kneading method and investigated by differential scanning calorimetry (DSC) and infrared spectroscopy (IR). Comparative dissolution studies indicated an over two-fold improvement in dissolution efficacy of the kneaded products, when compared to the pure drug. Results of the present study might pave the way for a drug formulation with improved bioavailability.     

Equilibrium and structural characterization of ofloxacin–cyclodextrin complexation

The enantiomer-specific characterization of ofloxacin–cyclodextrin complexes was carried out by a set of complementary analytical techniques. The apparent stability constants of the ofloxacin enantiomers with 20 different cyclodextrins at two different pH values were determined to achieve good resolution capillary electrophoresis enantioseparation either to establish enantioselective drug analysis assay, or to interpret and design improved host–guest interactions at the molecular level. The cyclodextrins studied differed in the nature of substituents, degree of substitution (DS), charge and purity, allowing a systematic test of these properties on the complexation. The seven-membered beta-cyclodextrin and its derivatives were found to be the most suitable hosts. Highest stability and best enantioseparation were observed for the carboxymethylated-beta-cyclodextrin (DS ~ 3.5). The effect of substitution pattern (SP) was investigated by molecular modeling, verifying that SP greatly affects the complex stability. Induced circular dichroism was observed and found especially significant on carboxymethylated-beta-cyclodextrin. The complex stoichiometry and the geometry of the inclusion complexes were determined by ¹H NMR spectroscopy, including 2D ROESY techniques. Irrespective of the kind of cyclodextrin, the complexation ratio was found to be 1:1. The alfa-cyclodextrin cavity can accommodate the oxazine ring only, whereas the whole tricyclic moiety can enter the beta- and gamma-cyclodextrin cavities. These equilibrium and structural information offer molecular basis for improved drug formulation.     

Photoinduced redox reactions between colloidal manganese dioxide and some organic compounds of environmental importance

Numerous organic compounds of environmental importance, i.e., phenol, citric, tartaric, and oxalic acids, proved to promote or accelerate reductive dissolution of colloidal manganese dioxide upon irradiation. This is accounted for the formation of surface-located charge-transfer complexes between the MnO₂ particulates and the organic electron donors. From the dependences of the rate of the photoassisted and thermal dissolution on the concentration of the organic compounds, the equilibrium constants for the formation of these complexes have been determined in the case of phenol, resorcinol, citrate, and tartaric acid. The quantum yields for these photoinduced reactions (at λ _ir = 365 nm), however, do not show any correlation with the values of the corresponding equilibrium constants, although adsorption is prerequisite for the efficient reductive dissolution of MnO₂. The changes in pH markedly affect the rate of this process, indicating that protonation of both the electron donors and the surface of the MnO₂ particulates may play significant roles in these systems. The results of experiments carried out in manganese dioxide excess suggest that total mineralization of organic electron donors is strongly hindered by the disadvantageous adsorption properties of the primary redox products. Dedicated to Professor Janos H. Fendler on the occasion of his 70th birthday.