SSZ-53 and SSZ-59: two novel extra-large pore zeolites

The syntheses, structure solutions, and physicochemical and catalytic characterizations of the novel zeolites SSZ-53 and SSZ-59 are described. SSZ-53 and SSZ-59 were synthesized under hydrothermal conditions with the [1-(4-fluorophenyl)cyclopentylmethyl]trimethyl ammonium cation and 1-[1-(4-chlorophenyl)cyclopentylmethyl]-1-methyl azocanium cation, respectively, as structure-directing agents. The framework topology of SSZ-53 was solved with the FOCUS method, and the structure of SSZ-59 was determined by model building. Rietveld refinement of synchrotron X-ray powder diffraction data confirms each proposed model. SSZ-53 and SSZ-59 each possess a one-dimensional channel system delimited by 14-membered rings. Results from transmission electron microscopy, electron diffraction, catalytic experiments (spaciousness index and constraint index tests), and argon and hydrocarbon adsorption experiments are consistent with the proposed structures.     

Transport processes in the sorption of colored ions by peat particles

A three-step model has been proposed for the adsorption of Astrazone Blue dye (Basic Blue 69) on peat. The initial rate of uptake of dye ions due to physical adsorption and chemisorption (ion exchange) has been correlated using a surface mass transfer coefficient. These coefficients have been determined and expressed in the dimensionless mass transfer form, Sh/Sc^0.33, as a function of agitation, initial dye concentration, peat particle size range, dye solution temperature, and mass of peat.     

Arene transition metal chemistry : III. Arene exchange phenomena

Arene exchange between free arene and an arene—transition metal complex is reviewed with respect to structure, thermodynamics, kinetics and reaction mechanism. Catalysis of such arene exchange is also examined. Experimental results are presented for arene exchange between arene and the arene—metal complexes: η⁶-arene-1,5-cyclooctadieneruthenium, the cationic η⁶-arene-1,5-cyclooctadieneiridium and η⁶-arenetricarbonylmolybdenum. Mechanistic features of these exchange reactions are discussed.     

Liquid chromatographic determination of diminazene diaceturate (Berenil) in raw bovine milk

A simple liquid chromatographic (LC) method is presented for the determination of diminazene (DZ) in raw bovine milk. DZ is extracted from raw milk by chilled aqueous centrifugation and is isolated from milk components on a cyano solid-phase extraction column. DZ is eluted by using a methanol-ion pairing reagent. A Phenomenex LUNA CN column and an acetonitrile-buffered mobile phase with a counter ion are used for gradient LC. The LC effluent is monitored at a detection wavelength of 372 nm by using a deuterium lamp. Under the parameters described, the retention time of DZ is 8-10 min with a peak area response of 6.5 mAU/ng. The method demonstrated excellent precision over all levels tested (25-400 ppb) with an overall average recovery of 90.4 +/- 14.5%. The method is applicable to the monitoring of milk for DZ residues at the 25 ppb level with a limit of quantitation of 10 ppb.     

Individually addressable submicron scale light-emitting devices based on electroluminescence of solid Ru(bpy)3(ClO4)2 films

A submicron light-emitting device (LED) was fabricated from lithographically fabricated parallel indium-tin oxide (ITO) finger electrodes (0.9 mum wide) separated by a 1.1 mum gap. A single layer of an amorphous (a) Ru(bpy)3(ClO4)2 film ( approximately 100 nm thick) was spin-coated on the electrode array. Ga:In or carbon paste was employed as a liftable upper contact electrode. Films ( approximately 1.5 mum thick) of single-crystal Ru(bpy)3(ClO4)2 (xyl) between two ITO electrodes in a sandwich cell were also prepared and produce electroluminescence. As with larger cells of this type, the high-resolution electroluminescence produced showed a high external efficiency ( approximately 3.4%), a low turn-on voltage (2.3 V), and reasonable stability. The single-crystal cells also behaved as photovoltaic devices and a short-circuit photocurrent was observed when they were irradiated without a bias voltage.     

Synthesis of the carbocyclic analogs of uracil nucleosides

Treatment of the required hydroxyl derivatives of cis-3-aminocyclopentanemethanol with 3-ethoxyacryloyl isocyanate gave N-(3-ethoxyacryloyl)-N′-[hydroxy- or dihydroxy(hydroxy-methyl)cyclopentyl]ureas. Cyclization of the ureas in dilute sulfuric acid afforded high yields of the carbocyclic analogs of uridine, 2′-deoxyuridine, and 3′-deoxyuridine. The uridine and 3′-deoxyuridine analogs were also obtained in good yields by cyclizing the ureas in concentrated aqueous ammonia. None of the three analogs showed activity in tests versus KB cells in culture or L1210 leukemia in vivo.