1975
DOI: 10.1021/ic50144a031
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New complexes of pentaamminechromium(III) with oxalate, glycinate, sulfate, and iodate as ligands. Loss of ammonia from chromium(III)-ammine complexes

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Cited by 31 publications
(13 citation statements)
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“…Ion-exchange separation of reactant solutions (for details see ref 6), over periods in which there was up to 50% consumption of Cr-(NH3)5H203+, indicated two products, Cr(NH3)5(02CCH2NH3)3+ and Cr(NH3)4(H20)(C>2CCH2NI43)3+, which have previously been characterized. 6 The kinetics were monitored at the 506-nm isosbestic point for the two products (t 39.8 M-1 cm-1). Concentration ranges Ka + [H+] (…”
Section: Methodsmentioning
confidence: 99%
“…Ion-exchange separation of reactant solutions (for details see ref 6), over periods in which there was up to 50% consumption of Cr-(NH3)5H203+, indicated two products, Cr(NH3)5(02CCH2NH3)3+ and Cr(NH3)4(H20)(C>2CCH2NI43)3+, which have previously been characterized. 6 The kinetics were monitored at the 506-nm isosbestic point for the two products (t 39.8 M-1 cm-1). Concentration ranges Ka + [H+] (…”
Section: Methodsmentioning
confidence: 99%
“…Homogeneous hydroxylation of metal ions and formation of metal ammine complex [8] from metal hydroxides are given by addition of urea caused by thermal decomposition of urea to ammonia. In addition, alcoholamines chelate metal ions [7,9].…”
Section: Chemical State and Viscosity Of Precursor Solsmentioning
confidence: 99%
“…Chromium (III) complexes are generally inert to the ligand substitution reactions 10 but reactions can be rapid under certain circumstances. Increased liability due to the presence of OH reported for Chromium (III) 11,12 . Lower enthalpy of activation for complexation reaction (92KJ mol -1 ) and large negative value of ∆S(-175JK -1 mol -1 ) suggest the more pronounced participation of incoming ligand in the transition state and confirm the transformation of the outer sphere complex into inner sphere complex 9 .…”
Section: Introductionmentioning
confidence: 99%