A Raman Spectroscopic Study of Aqueous La(CH<sub class="a-plus-plus">3sub>CO<sub class="a-plus-plus">2sub>)<sub class="a-plus-plus">3sub> Solutions and La(CH<sub class="a-plus-plus">3sub>CO<sub class="a-plus-plus">2sub>)<sub class="a-plus-plus">3sub>·1.5 H<sub class="a-plus-plus">2sub>O(cr)

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• 作者：Wolfram W. Rudolph ; Gert Irmer
• 关键词：Raman spectroscopy ; Density functional theory ; La(CH3CO2)3(aq) ; La(CH3CO2)3·1.5H2O(cr) ; Bidentate La3+ acetato complex species ; Equilibrium constant K1
• 刊名：Journal of Solution Chemistry
• 出版年：2017
• 出版时间：January 2017
• 年：2017
• 卷：46
• 期：1
• 页码：190-214
• 全文大小：
• 刊物类别：Chemistry and Materials Science
• 刊物主题：Physical Chemistry; Industrial Chemistry/Chemical Engineering; Geochemistry; Oceanography; Inorganic Chemistry; Condensed Matter Physics;
• 出版者：Springer US
• ISSN：1572-8927
• 卷排序：46

文摘

Aqueous solutions of La(CH<sub>3sub>CO<sub>2sub>)<sub>3sub>, NaCH<sub>3sub>CO<sub>2sub> and La(ClO<sub>4sub>)<sub>3sub> were studied using Raman spectroscopy. In dilute NaCH<sub>3sub>CO<sub>2sub> solution, acetate is fully hydrated and forms only minor amounts of ion pairs. The characteristic Raman bands are discussed and assigned. In fairly dilute La(ClO<sub>4sub>)<sub>3sub> solutions, the La3+(aq) ion occurs as the nonahydrate. The separation of the carboxylate bands, ν<sub>assub> – ν<sub>ssub> (Δ-value), in NaCH<sub>3sub>CO<sub>2sub>(cr) compared to La(CH<sub>3sub>CO<sub>2sub>)<sub>3sub>·1.5H<sub>2sub>O(cr) correlates with the bonding type of acetate which is “ionic” in the former but bidentate chelating/tridentate chelating in the latter. Other acetate bands such as the deformation mode of the CO<sub>2sub> moiety, δ CO<sub>2sub>, and the two rocking vibrations (ρ), as well as the C–C stretch show marked differences in their band positions in NaCH<sub>3sub>CO<sub>2sub>(cr) compared to the ones in La(CH<sub>3sub>CO<sub>2sub>)<sub>3sub>·1.5H<sub>2sub>O(aq). In a ternary solution of La(CH<sub>3sub>CO<sub>2sub>)<sub>3sub>/LaCl<sub>3sub> with a molar ratio La3+(aq): \( {\text{CH}}_{3} {\text{CO}}_{2}^{ - } \)(aq) = 3.87: 1.00), the bands of the bound acetate on La3+ were characterized and compared to those of fully hydrated acetate, \( {\text{CH}}_{3} {\text{CO}}_{2}^{ - } \left( {\text{aq}} \right) \). In this solution, almost all acetate is ligated to La3+ in a bidentate fashion and two complex species could be identified (molar ratios La3+: \( {\text{CH}}_{3} {\text{CO}}_{2}^{ - } \)  = 1:1 and 1:2, respectively). In La(CH<sub>3sub>CO<sub>2sub>)<sub>3sub> solutions in H<sub>2sub>O and D<sub>2sub>O strong acetato complexes are formed and the bands of the bound acetate were characterized and compared with the ones of the fully hydrated acetate modes. A dilution series down to 0.0037 mol·L−1 in La(CH<sub>3sub>CO<sub>2sub>)<sub>3sub>(aq) and to 0.0150 mol·L−1 in La(CH<sub>3sub>CO<sub>2sub>)<sub>3sub>(D<sub>2sub>O) showed that two acetate complexes are formed in these solutions. Again, it was shown that in these solutions the bound acetates on La3+ exist as bidentate ligands. DFT frequencies of the acetate on clusters {La(OH<sub>2sub>)<sub>7sub>O<sub>2sub>CCH<sub>3sub>)}2+ and {La(OH<sub>2sub>)<sub>5sub>(O<sub>2sub>CCH<sub>3sub>)<sub>2sub>}+ compared well with the measured values. By determining the ligation number, \( \bar{n} \), it can be established that in dilute solutions, below 0.04 mol·L−1, a complex with a 1:1 stoichiometry (La3+: \( {\text{CH}}_{3} {\text{CO}}_{2}^{ - } \)) exists in equilibrium with “free” acetate while in more concentrated solutions a 1:2 complex also forms. La3+(aq) hydrolysis is slight and very small equilibrium concentrations of CH<sub>3sub>COOH were detected (C–C stretch at 893 cm−1). From quantitative Raman measurements, K<sub>1sub> was determined to be 160 ± 10 at 22 °C.