Galli

Galli C, Wynne K, LeCours S, Therien M J and Hochstrasser R M 1993 Direct measurement of electronic dephasing using anisotropy Chem. Phys. Lett. 206 493-9... 

Wynne K, Galli C and Hochstrasser R M 1994 Ultrafast charge transfer in an electron donor-acceptor complex J. Cham. Phys. 100 4796-810... 

Ghristian, G. D. Gallis, J. B. eds. Trace Analysis and Spectroscopic Methods for Molecules. Wiley-lnterscience New York, 1986. 

Gallie, R.R. and Hewitt, P.V., Eighteen years of operating and development experience with Windseale AGR, Nucl. Energy, 1982, 21,21 28. 

G. Galli, A. Pasquarello. In M. P. Allen, D. J. Tildesley, eds. Computer Simulation in Chemical Physics. Dordrecht NATO-ASI series 597, Kluwer Academic, 1993, p. 261. 

One should perhaps mention some other closures that are discussed in the literature. One possibility is to combine the PY approximation for the hard core part of the potential and then use the HNC approximation to compute the corrections due to the attractive forces. Such an approach is called the reference hypernetted chain or RHNC approximation [48,49]. Recently, some new closures for a mixture of hard spheres have been proposed. These include one by Rogers and Young [50] (RY) and the Martynov-Sarkisov [51] (MS) closure as modified by Ballone, Pastore, Galli and Gazzillo [52] (BPGG). The RY and MS/BPGG closure relations take the forms... 

E. Meinjohanns, M. Meldal, T. Jensen, O. Werdelin, L. Galli-Stampino,... 

G. Gottard and E. Galli, Natural Zeolites, Springer-Verlag, Berlin, 1985, 400 pp. P. A. Jacobs and... 

JHC327 G. Sorba, G. Ermondi, R. Eruttero, U. Galli, and A. Gasco, J. Heterocycl. 

Galli-. gallic (relating to trivalent gallium), -chlorid, n. gallic chloride, gallium (III) chloride. 

R Bellissent, G. Galli, T. Hyeon, S. Magazu, D. Majolino, P. Migliardo, and K. S. Suslick, Structural properties of amorphous bulk Fe, Co and Fe-Co binary alloys, Physica Scripta, T57 79(1995). 

Chiellini, E., Solaro, R., Galli,G. and Ledwith, A. Optically Active Synthetic Polymers Containing Pendant Carbazolyl Groups. Vol. 62, pp. 143 — 170. 

Fig. 8-7. Dependence of the yield in chloro-de-diazoniations on the redox potential of electron transfer reagents (from Galli, 1988 Fc = ferrocene).

Gilbert et al. (1992, see also Galli, 1988) showed that a dual substituent parameter treatment (DSP, see Sec. 7.2) gave the best fit to the influence of substituents as measured by Doyle et al. (1987 a) with Fe(CN)6, as well as for reactions with the ferro complex of ethenediaminetetraacetic acid (Fen-EDTA). 

More recently Broxton and McLeish (1983 b) postulated that the aryldiazene is formed by direct hydride transfer from the methoxide ion to the diazonium ion (Scheme 8-53). In the opinion of Galli (1988, p. 775), and also of the present author, this and the following reactions can hardly compete with the chain reaction discussed above. 

Table 10-1. Yield of chlorobenzene in chloro-de-diazoniation of benzenediazonium sulfate as a function of electron transfer reagent and ligand transfer reagent. Experiments 1-5 from Galli, 1981a), experiment 6 from Daasbjerg and Lund, 1992b).

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