2009
DOI: 10.1016/j.inoche.2009.08.016
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A new synthetic route towards a Ru(III) substituted heteropolytungstate anion

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Cited by 24 publications
(24 citation statements)
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“…[ is S-bonded to ruthenium, as confirmed by 31 P NMR [24] and EPR spectroscopy [32] (for X = P), as well as single-crystal Xray diffraction (for X = Si; Figure 6 a) [33] and by DFT calculations. [34] A detailed electrochemical investigation [24] [*] We note that for L-structure complexes involving large secondary heteroatoms (lanthanides and actinides) the number of free coordination sites increases up to four.…”
mentioning
confidence: 69%
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“…[ is S-bonded to ruthenium, as confirmed by 31 P NMR [24] and EPR spectroscopy [32] (for X = P), as well as single-crystal Xray diffraction (for X = Si; Figure 6 a) [33] and by DFT calculations. [34] A detailed electrochemical investigation [24] [*] We note that for L-structure complexes involving large secondary heteroatoms (lanthanides and actinides) the number of free coordination sites increases up to four.…”
mentioning
confidence: 69%
“…[56] Salts of these complexes were characterized by elemental analysis, 31 confirmed by analytical ultracentrifugation and X-ray structure analysis of the potassium salt (Figure 6 d) 5À and dibenzyl under prolonged (5 h) photolysis at ambient temperature. [56] No benzylrhodium species were detected as products in the photolysis, but rhodium-carbon bond formation occurred in hydrothermal reactions of aqueous solutions of lacunary heteropolytungstates with RhCl 3 in 0.…”
Section: Rhodiummentioning
confidence: 86%
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