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Hydrogen ionization potential

Heats of Hydrogenation, Ionization Potential, Net Charge, and Dipole Moment 313... [Pg.299]

The period 1996-2006 did not appear to have papers concerned with heats of hydrogenation, ionization potential, or net charge of thiiranes or thiirenes. [Pg.313]

Use MNDO, AMI, and PM3 (MOPAC, ccl.net) to determine the ionization potential of the hydrogen atom... [Pg.281]

Ultraviolet photoelectron spectroscopy allows the determination of ionization potentials. For thiazole the first experimental measurement using this technique was preformed by Salmona et al. (189) who later studied various alkyl and functional derivatives in the 2-position (190,191). Substitution of an hydrogen atom by an alkyl group destabilizes the first ionization potential, the perturbation being constant for tso-propyl and heavier substituents. Introduction in the 2-position of an amino group strongly destabilizes the first band and only slightly the second. [Pg.51]

Elemental boron has a diverse and complex chemistry, primarily influenced by three circumstances. Eirst, boron has a high ionization energy, 8.296 eV, 23.98 eV, and 37.75 eV for first, second, and third ionization potentials, respectively. Second, boron has a small size. Third, the electronegativities of boron (2.0), carbon (2.5), and hydrogen (2.1) are all very similar resulting in extensive and unusual covalent chemistry. [Pg.183]

The PE spectra of simple diaziridines exhibit two bands at lower ionization potentials these are assumed to arise from removal of an electron from one or other of the lone pair MOs. An E arrangement of the two N-bound hydrogens in 3,3-dimethyldiaziridine (37a) is assumed, since the difference of the ionization potentials (0.51 eV) is much smaller than in the fused diaziridine (42) (1.40 eV) which necessarily has the Z configuration (73HCA1614). [Pg.202]

Platinum-cobalt alloy, enthalpy of formation, 144 Polarizability, of carbon, 75 of hydrogen molecule, 65, 75 and ionization potential data, 70 Polyamide, 181 Poly butadiene, 170, 181 Polydispersed systems, 183 Polyfunctional polymer, 178 Polymerization, of butadiene, 163 of solid acetaldehyde, 163 of vinyl monomers, 154 Polymers, star-shaped, 183 Polymethyl methacrylate, 180 Polystyrene, 172 Polystyril carbanions, 154 Potential barriers of internal rotation, 368, 374... [Pg.410]

The properties of the hydrogen molecule and molecule-ion which are the most accurately determined and which have also been the subject of theoretical investigation are ionization potentials, heats of dissociation, frequencies of nuclear oscillation, and moments of inertia. The experimental values of all of these quantities are usually obtained from spectroscopic data substantiation is in some cases provided by other experiments, such as thermochemical measurements, specific heats, etc. A review of the experimental values and comparison with some theoretical... [Pg.24]

IH, the ionization potential of hydrogen, accordingly is equal to 13.54 volts. [Pg.32]

As for Erep, Ect is derived from an early simplified perturbation theory due to Murrel [46], Its formulation [47,48] also takes into account the Lrj lone pairs of the electron donor molecule (denoted molecule A). Indeed, they are the most exposed in this case of interaction (see Section 6.2.3) and have, with the n orbital, the lowest ionization potentials. The acceptor molecule is represented by bond involving an hydrogen (denoted BH) mimicking the set, denoted < > bh, of virtual bond orbitals involved in the interaction. [Pg.157]

Activation Energies for Hydrogenation, and First Ionization Potentials, for some Aromatic Hydrocarbons... [Pg.150]

Unlike hydrogen these reactions do not appear to be activated. In addition the products distributions observed indicate comparable rates for multiple adduct formation. The mass complexity, relatively high ionization potentials, and the known prevalent dissociative ionization of the fully saturated carbonyls(42) has possibly caused the failure of some initial saturation experi ments(43). The ability to synthesize the stable carbonyl complexes will help this field significantly due to the vast amount of information available, especially their structures. [Pg.58]


See other pages where Hydrogen ionization potential is mentioned: [Pg.7]    [Pg.7]    [Pg.27]    [Pg.383]    [Pg.100]    [Pg.95]    [Pg.375]    [Pg.525]    [Pg.873]    [Pg.394]    [Pg.324]    [Pg.116]    [Pg.198]    [Pg.240]    [Pg.45]    [Pg.26]    [Pg.17]    [Pg.344]    [Pg.238]    [Pg.171]    [Pg.99]    [Pg.3]    [Pg.5]    [Pg.6]    [Pg.7]    [Pg.189]    [Pg.20]    [Pg.329]    [Pg.120]    [Pg.142]    [Pg.149]    [Pg.649]   
See also in sourсe #XX -- [ Pg.179 ]

See also in sourсe #XX -- [ Pg.177 ]

See also in sourсe #XX -- [ Pg.67 , Pg.93 ]

See also in sourсe #XX -- [ Pg.165 ]




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