1969
DOI: 10.1007/bf00906372
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Chloride complexes of rhodium (III) in aqueous solutions

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Cited by 5 publications
(2 citation statements)
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“…The photoabsorption in the range around 450 nm originated from d−d transition of Rh, 1 A 1g → 2 T 2g . 11,34 The photoabsorption in the range from visible to UV light regions probably originated from the charge transfer from Rh 3+ to the conduction band of semiconductors, which depends on the semiconductor oxide.…”
Section: Electrochemical Measurements Under Irradiation Of Visiblementioning
confidence: 99%
“…The photoabsorption in the range around 450 nm originated from d−d transition of Rh, 1 A 1g → 2 T 2g . 11,34 The photoabsorption in the range from visible to UV light regions probably originated from the charge transfer from Rh 3+ to the conduction band of semiconductors, which depends on the semiconductor oxide.…”
Section: Electrochemical Measurements Under Irradiation Of Visiblementioning
confidence: 99%
“…This method was extensively studied for the recovery of noble metals, mainly gold [29,30] and platinum [31][32][33]. Bromide anions were selected as the complexing agent because the stability of the complex ion is lower when compared to the chloride one [34,35]. This offers, at least theoretically, the possibility of adsorption and subsequent reduction of Rh(III) to the metallic form as it was observed in the case of Au(III) chloride complex ions [36][37][38][39].…”
Section: Introductionmentioning
confidence: 99%