2020
DOI: 10.1039/d0ra05339b
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Extraction of Pd(ii) and Pt(ii) from aqueous hydrochloric acid with 1,3-diaminocalix[4]arene: switching of the extraction selectivity by using different extraction modes

Abstract: 1,3-Diaminocalix[4]arene shows extraction ability toward Pd(ii) and Pt(ii), the selectivity of which can be switched by changing the concentrations of H+ and Cl− in the aqueous phase.

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Cited by 6 publications
(8 citation statements)
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“…Analysis of high-field 1 H and 13 C NMR spectra of the products demonstrate that sets of proton and carbon chemical shifts and proton-proton and carbon-proton spin-spin couplings for each compound are similar to those of the previously reported structurally relative bis(a-amine oximes). 41,42 The chemical purity of the compounds (96-99%) was assessed by 1 H NMR from the carbon-13 satellite signals.…”
Section: Synthesis and Characterizationsupporting
confidence: 74%
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“…Analysis of high-field 1 H and 13 C NMR spectra of the products demonstrate that sets of proton and carbon chemical shifts and proton-proton and carbon-proton spin-spin couplings for each compound are similar to those of the previously reported structurally relative bis(a-amine oximes). 41,42 The chemical purity of the compounds (96-99%) was assessed by 1 H NMR from the carbon-13 satellite signals.…”
Section: Synthesis and Characterizationsupporting
confidence: 74%
“…Nuclear magnetic resonance (NMR) spectra were recorded at 27-30 1C for solutions (c 10-40 mg mL À1 ) on a Bruker AV 300 and a Bruker DRX-500 spectrometer (300. 13 Signal assignment was made using J modulated 13 C NMR spectra (proton-noise-decoupling, the opposite phases for the signals of the atoms with the odd and even numbers of the attached protons, tuning to the constant J = 135 Hz). The signals of N-H and O-H groups were determined by polarization transfer upon saturation of the HDO signal of the water traces in the solvent used.…”
Section: Instruments and Methodsmentioning
confidence: 99%
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