Effect of Some Macrocyclic Ligands on the Rate of Reduction of Perchlorate Ion by Titanium(III)
Giulio A. Amadei
; Department of Chemistry, Georgetoivn University, Washington DC 20057, USA
Joseph E. Earley, Sr.
; Department of Chemistry, Georgetoivn University, Washington DC 20057, USA
APA 6th Edition Amadei, G.A. i Earley, Sr., J.E. (2001). Effect of Some Macrocyclic Ligands on the Rate of Reduction of Perchlorate Ion by Titanium(III). Croatica Chemica Acta, 74 (3), 601-606. Preuzeto s https://hrcak.srce.hr/131869
MLA 8th Edition Amadei, Giulio A. i Joseph E. Earley, Sr.. "Effect of Some Macrocyclic Ligands on the Rate of Reduction of Perchlorate Ion by Titanium(III)." Croatica Chemica Acta, vol. 74, br. 3, 2001, str. 601-606. https://hrcak.srce.hr/131869. Citirano 06.03.2021.
Chicago 17th Edition Amadei, Giulio A. i Joseph E. Earley, Sr.. "Effect of Some Macrocyclic Ligands on the Rate of Reduction of Perchlorate Ion by Titanium(III)." Croatica Chemica Acta 74, br. 3 (2001): 601-606. https://hrcak.srce.hr/131869
Harvard Amadei, G.A., i Earley, Sr., J.E. (2001). 'Effect of Some Macrocyclic Ligands on the Rate of Reduction of Perchlorate Ion by Titanium(III)', Croatica Chemica Acta, 74(3), str. 601-606. Preuzeto s: https://hrcak.srce.hr/131869 (Datum pristupa: 06.03.2021.)
Vancouver Amadei GA, Earley, Sr. JE. Effect of Some Macrocyclic Ligands on the Rate of Reduction of Perchlorate Ion by Titanium(III). Croatica Chemica Acta [Internet]. 2001 [pristupljeno 06.03.2021.];74(3):601-606. Dostupno na: https://hrcak.srce.hr/131869
IEEE G.A. Amadei i J.E. Earley, Sr., "Effect of Some Macrocyclic Ligands on the Rate of Reduction of Perchlorate Ion by Titanium(III)", Croatica Chemica Acta, vol.74, br. 3, str. 601-606, 2001. [Online]. Dostupno na: https://hrcak.srce.hr/131869. [Citirano: 06.03.2021.]
Sažetak Complexation with cyclam increases the rate of reduction of perchlorate ion by TiIII (in acidic, aqueous, 4 mol dm-3 LiCl Solutions at 25 °C) relative to the rate of the corresponding reduction of Ti3+. A modified cyclam with pendant amine and p-aminobenzyl functional groups is more effective in this regard than is cyclam itself. Both redox reactions are acid catalyzed. The data is consistent with involvement of an intermediate containing two TiIII centers.