Synthesis and Characterisation of New Arsonium Salts and Crystal Structures of Trimethylarsonium Undecafluorodiarsenate (CH3)3AsH+As2F11− and Trimethylarsonium Hexafluoroantimonate (CH3)3AsH+SbF6−
✍ Scribed by Rolf Minkwitz; Claudia Hirsch; Thorsten Berends
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 291 KB
- Volume
- 1999
- Category
- Article
- ISSN
- 1434-1948
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✦ Synopsis
The reaction of trimethylarsane in the superacidic systems As 2 F 11 -crystallizes in the monoclinic space group P2 1 /n with four formula units per unit cell with the dimensions a = hydrogen/fluoride antimony pentafluoride and hydrogen fluoride/arsenic pentafluoride leads to trimethylarsonium 7.362(1), b = 12.589(1), c = 13.598(1) A ˚and β = 95.37(1)°.
(CH 3 ) 3 AsH + SbF 6 -crystallizes in the monoclinic space group fluorometallates. These salts are stable up to 60 °C and 5 °C, respectively. Structures were successfully elucidated in the P2 1 /m with four formula units per unit cell with the dimensions a = 8.313(1), b = 8.855(1), c = 13.285(1) A ˚and cases of trimethylarsonium undecafluorodiarsenate and trimethylarsonium hexafluoroantimonate.
(CH 3
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## Abstract The preparation of a family of dinuclear monocyclopentadienyl imidoniobium and ‐tantalum complexes was achieved by two different synthetic routes. The diimido complexes [{M(Cp′)Cl~2~}~2~(μ‐1,__i__‐NC~6~H~4~N)] [Cp′ = η^5^‐C~5~H~4~SiMe~3~, M = Nb, __i__ = 4 (1); Cp′ = η^5^‐C~5~H~4~SiMe~3