1968
DOI: 10.1021/ja01021a072
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The relative fluoride ion donor abilities of XeF2, XeF4, and XeF6 and a chemical purification of XeF4

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Cited by 46 publications
(31 citation statements)
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“…[5] The first coordination compound with a noble-gas fluoride acting as a ligand to a metal ion was [Ag(XeF 2 ) 2 ]AsF 6 . [6] A series of such coordination compounds has since been prepared, [7] but coordination compounds with XeF 4 , (a poorer Lewis base or less thermally stable than XeF 2 [8] ) as a metal ion ligand, were not known.…”
Section: In Memory Of Neil Bartlettmentioning
confidence: 99%
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“…[5] The first coordination compound with a noble-gas fluoride acting as a ligand to a metal ion was [Ag(XeF 2 ) 2 ]AsF 6 . [6] A series of such coordination compounds has since been prepared, [7] but coordination compounds with XeF 4 , (a poorer Lewis base or less thermally stable than XeF 2 [8] ) as a metal ion ligand, were not known.…”
Section: In Memory Of Neil Bartlettmentioning
confidence: 99%
“…At the molar ratio XeF 2 :Mg = 2:1 or higher the only product was [Mg(XeF 2 ) 2 ]-(AsF 6 ) 2 , which is in accord with the lower Lewis basicity of XeF 4 . [8] The magnesium ion is surrounded by six fluorine atoms, four from [AsF 6 ] À units, one from XeF 2 , and one from XeF 4 ( Figure 1 À unit is trans bridging, whereas the [As2F 6 ] À unit is a cis bridging in the complex. In both cases, the bridging As À F distances are elongated.…”
Section: In Memory Of Neil Bartlettmentioning
confidence: 99%
“…Yellow arsenic, obtained by sudden cooling of arsenic vapour, is assumed to consist of AS4 molecules. It can be recrystallized from carbon disulphide (solubility: 11 g in 100 ml at 46°C; 4 g at 0°C; 0.8 g at -80°C) but is rapidly converted to grey arsenic in light, and very easily oxidized 5 . Above 300°C, arsenic vapour condenses as grey arsenic, but, at 100-200°C, glassy modifications result.…”
Section: Fig 1 Plan Of a Sheet Of Atoms In Rhombohedral Arsenic Atmentioning
confidence: 99%
“…The compounds AS2H4, AS2H5 and Sb 2 H 4 have been made only in very low yields, and so information about them is limited 5 <>. The catenated compounds are isolated as byproducts in the preparation of the trihydrides from metal arsenides or antimonides or from borohydride reductions.…”
Section: Lower Hydridesmentioning
confidence: 99%
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