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Linnett

There are a number of three- to five-parameter potential functions in the literature, of which the Morse potential is the most popular a typical five-parameter potential is the Linnett function (Linnett, 1940, 1942) ... [Pg.37]

Linnett and Rosenberg have discussed the electronic structure of a number of nitroso and potential nitroso systems, including benzo-furoxans, using the non pairing approach. ... [Pg.6]

Fig. 6. Side-arm tube of the apparatus for the determination of the coefficients of the heterogeneous recombination, y, of atomic gases previously dissociated in the rf discharge zone. The heterogeneous recombination proceeds on the inner glass walls of the horizontal side-arm tube and on a catalytically active cylindric sample of the metal investigated (Smith-Linnett method). Fig. 6. Side-arm tube of the apparatus for the determination of the coefficients of the heterogeneous recombination, y, of atomic gases previously dissociated in the rf discharge zone. The heterogeneous recombination proceeds on the inner glass walls of the horizontal side-arm tube and on a catalytically active cylindric sample of the metal investigated (Smith-Linnett method).
The kinetic equation obtained experimentally is of the first order, in the case of the Smith-Linnett method, thus serving for confirmation of the mechanism proposed. [Pg.260]

Hardy and Linnett (59) studied the heterogeneous recombination of atomic hydrogen at room temperature on nickel and nickel alloy foils. They did not find any similarity to the behavior of palladium and its alloys with gold studied earlier (35). There was no evidence that, as a result of exposure to atomic hydrogen, hydride was formed in any metal catalyst investigated with a resulting change in the activity of the initial parent metal catalysts. [Pg.273]

Thus nickel and nickel-copper alloy films evaporated in vacuo onto the inner walls of the reaction vessel have been chosen for further investigations. The films were deposited onto the inner wall of a glass tube kept at 450°C their thickness amounted to approximately 2000 A. After annealing at the same temperature in vacuo they were transferred into the side-arm of the Smith-Linnett apparatus in order for the recombination coefficients to be determined. The bulk homogeneity of alloy films prepared in this way was confirmed by X-ray diffraction (65, 65a, 66). [Pg.279]

This conclusion was additionally confirmed by Palczewska and Janko (67) in separate experiments, where under the same conditions nickel-copper alloy films rich in nickel (and nickel films as well) were transformed into their respective hydride phases, which were proved by X-ray diffraction. The additional argument in favor of the transformation of the metal film into hydride in the side-arm of the Smith-Linnett apparatus consists of the observed increase of the roughness factor ( 70%) of the film and the decrease of its crystallite size ( 30%) after coming back from low to high temperatures for desorbing hydrogen. The effect is quite similar to that observed by Scholten and Konvalinka (9) for their palladium catalyst samples undergoing the (a — j8) -phase transformation. [Pg.280]

There are other methods. For a discussion of the free-electron method, see Streitwieser Jr., A. Molecular Orbital Theory for Organic Chemists Wiley NY, 1961, p. 27. For the nonpairing method, in which benzene is represented as having three electrons between adjacent carbons, see Hirst, D.M. Linnett, J.W. J. Chem. Soc., 1962,1035 Firestone, R.A. J. Org. Chem., 1969, 34, 2621. [Pg.78]

J. W. Linnett. There were 11 papers with theoretical inputs but with more emphasis given to new developments in experimental methods including structural (LEED and electron microscopy) and surface spectroscopies. LEED provided crucial evidence for the role of surface steps at platinum single crystals in the dissociation of various diatomic molecules, while electron microscopy revealed the role of dislocations as sites of high reactivity of... [Pg.7]

Linnett used the concept that an octet of valence shell electrons consists of two sets of four opposite-spin electrons to show that in diatomic and other linear molecules the two tetrahedra are not in general formed into four pairs as we have discussed for F2 and the CC triple bond in C2H2. This idea is the basis of the double-quartet model, which Linnett applied to describe the bonding in a variety of molecules. It is particularly useful for the description of the bonding in radicals, including in particular the oxygen molecule, which has two unpaired electrons and is therefore paramagnetic This unusual property is not explained by the Lewis structure... [Pg.102]

Linnett, J. W. The Electronic Structure of Molecules A New Approach Methuen London, 1964. [Pg.279]

Linnett, J. W. (1964). The electronic structure of molecules. London Methuen. [Pg.298]


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See also in sourсe #XX -- [ Pg.87 , Pg.102 , Pg.171 ]

See also in sourсe #XX -- [ Pg.141 ]

See also in sourсe #XX -- [ Pg.87 , Pg.102 , Pg.171 ]

See also in sourсe #XX -- [ Pg.9 ]




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