An addition to the oxoacid family: H2B12(OH)12

The acid H(2)B(12)(OH)(12) can be isolated as a crystalline solid by protonation of the hydroxylated borane anion, B(12)(OH)(12)(2)(-). This acidic compound has low solubility in water, conducts protons in the solid state, and has thermal stability to a temperature of 400 degrees C. The conductivity mechanism is a Grotthuss mechanism with a low activation enthalpy (9-13 kcal/mol). This new acid represents an addition to the class of oxoacids, of which sulfuric and phosphoric acid are the most prominent examples.     

Coordination complexes of acetylenic phosphines and diphosphines

The reactions of π-cyclopentadienylnickel carbonyl dimer with 3,3,3-trimethylpropynyldiphenylphosphine and phenylethynyldiphenylphosphine are described. The products have been characterized by elemental and mass spectral analysis, infrared and NMR spectroscopy. An acetylene bridged complex (π-C₅H₅Ni)₂Ph₂PC₂-t-Bu, containing an uncoordinated phosphorus atom, has been prepared. The complex can be oxidized to the phosphine oxide derivative (π-C₅H₅Ni)₂Ph₂P(O)C₂-t-Bu and converted to the phosphonium salts with methyl iodide or ethyl bromide. These are the first reported π-complexes of phosphonium salts. The complex (π-C₅H₅Ni)₂Ph₂PC₂-t-Bu forms the novel mixed metal derivative [PdCl₂][(π-C₅H₅Ni)₂Ph₂PC₂-t-Bu]₂ from bis(benzonitrile)-palladium dichloride. The dicarbonyl complexes Ni(CO)₂(Ph₂PC₂R)₂ (R  t-Bu, Ph), the phosphine oxide complex (π-C₅H₅Ni)₂(Ph₂P(O)C₂Ph) and the trinuclear nickel carbonyl derivative Ni(CO)₃[(π-C₅H₅Ni)₂Ph₂PC₂Ph] are described.     

Experimental measurement and prediction of hydrate forming conditions in the nitrogen-propane-water system

Experimental data on initial hydrate formation conditions have been obtained for the nitrogen-propane-water system in the L₁HG, L₁L₂H, and L₁L₂HG regions, where L₁ is the water rich liquid phase, L₂ is the hydrocarbon rich liquid phase, H is the hydrate and the G is the vapor phase. The measurements covered a range of temperatures from about 275 to 293 K and pressures from about 0.3 to 17.0 MPa. The concentrations covered for the L₁HG region extended from 0.94 to 75.0 mole percent propane in the gas phase, and for the L₁L₂H region they extended from 83.1 to 99.0 mole percent in the condensed liquid phase. Four-phase measurements were made at concentrations of propane from 18.1 to 71.1 mole percent in the gas phase.The experimental data were used to find a fitted binary interaction parameter for predicting hydrate formation in systems containing nitrogen and propane.