Hydroxy Oxime in - American Chemical Society

(22) Tetsuo Miyazatki and Takeshi Hirayama, J. Phys. Chem., 79, 566. (10) T. J. Klingen and M. A. Mathur, J. Inorg. Nucl. Chem., 39, 1477. (1 1) D. G...
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(16) R. S. Porter, E . M. Barrel1 11, and J. F. Johnson, Acc. Chem. Res., 2, 53 (1969). (17) J. E. Willard, Org. Solid State Chem., (1969). (18) S. 0. Lias and P. Ausloos, "Ion-Molecule Reactions, Their Role In Radiation Chemistry", Amerlcan Chemical Society, Washington, D.C., 1975. (19) R. Srinivasan, J . Am. Chem. SOC.,83, 2590 (1961). (20) R. Srinlvasan, J . Am. Chem. Soc., 81, 1546 (1959). (21) R. Srlnivasan, J. Am. Chem. SOC.,81, 2604 (1959). (22) Tetsuo Miyazatki and Takeshi Hirayama, J . Phys. Chem., 79, 566 (1975).

(10) T. J. Klingen and M. A. Mathur, J . Inorg. Nucl. Chem., 39, 1477 (1977). (11) D. G. McCormick, L. R. Sherman, and T. J. Klingen, Radlat. Phys. Chem., 15, 677 (1980). (12) 6.Tadros and K. Leupin, Pharm. Actat Helv., 40, 407 (1965). (13) J. Gloux, M. Guglielmix, and H. Lemaire, Mol. phys., 19, 833 (1970). (14) C. J. Hochanadel and J. A. Ghormley, J. Chem. Phys., 21, 880 (1953). (15) J. 0. Aston in "Physics and Chemistry of the Organic Solid State", Vol. I, D. IFOX,M. hh. Labes, and A. Weissberger, Eds., Intersclence, New York, 1963, p 549.

Kinetics and Mechanism of the Complex Formation Reactions between Cu(I1) and Fe(II1) Aqueous Speclies ernd a @-HydroxyOxime in Toluene P. R. Danesl,*f R. Chiarlzla,' and 0. F. Vandegrlftf Cheniistty Division, Argonne National Laboratory, Argonne, Illinois 60439, and Laboratorlo Chimlca Flsica, RIT-MAT, Caseccla, C.N.E.N., Romn, Italy (Received: Mvch 25, 1960; In Final Form: August 6, 1980)

The kinetics of the complex formation reaction between Cu(I1) and Fe(II1) aqueous species, present in a 2 M C1- nnedium, and a P-hydroxy oxime (2-hydroxy-5-tert-octylacetophenone oxime) dissolved in toluene has been studied by using a highly stirred apparatus which allows the contribution of interfacial film diffusion processes to the measured rate t,o be assumed equal to zero. The results obtained have indicated that the reactions take place -- at the interface. The following rate laws have been measured: -d[Cu(II)],,/dt - = k~