1990
DOI: 10.1002/chin.199005034
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ChemInform Abstract: Synthesis and Crystal Structure of Nitrosofluorotetrammines of Osmium and Ruthenium.

Abstract: Starting from (MNO(NH3)4OH) (NO2)2 (M: Ru, Os) or from (MNOF5) (NO2)2, whose cations are converted to (MNO(NH3)4F)2+ on treatment with NH4HF2 at 200 °C, the hitherto unknown title compounds (I)‐(IV) are prepared.

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“…The co‐crystallized (HF 2 ) – anion shows resonances at 1278 and 1215 cm –1 [ν 2 (E)] and 655 cm –1 [ν 1 (A 1 g)], the assignment of which was done with respect to the spectrum of NaHF 2 16. Hydrogen bonds of the type F ··· H–N between ammine ligands and the [TcF 6 ] 2– counterion can be assigned with reference to the IR spectra of [M(NO)(NH 3 ) 4 F][SiF 6 ] 17. The Tc–NO vibration gives a band at 602 cm –1 .…”
Section: Resultsmentioning
confidence: 99%
“…The co‐crystallized (HF 2 ) – anion shows resonances at 1278 and 1215 cm –1 [ν 2 (E)] and 655 cm –1 [ν 1 (A 1 g)], the assignment of which was done with respect to the spectrum of NaHF 2 16. Hydrogen bonds of the type F ··· H–N between ammine ligands and the [TcF 6 ] 2– counterion can be assigned with reference to the IR spectra of [M(NO)(NH 3 ) 4 F][SiF 6 ] 17. The Tc–NO vibration gives a band at 602 cm –1 .…”
Section: Resultsmentioning
confidence: 99%
“…In the next step, the resulting yellow crystalline powder with presumed formula trans-[RuNO(NH 3 ) 4 F](H n F n+1 ) 2 was dissolved in water in a glass tube, leading to the formation of trans-[RuNO(NH 3 ) 4 F]SiF 6 single crystals. In an earlier report on the synthesis of trans-[RuNO(NH 3 ) 4 F] 2+ (Sinitsyn et al, 1989), the precursor complexes trans-[RuNO(NH 3 ) 4 OH]-(NO 2 ) 2 or K 2 [RuNOF 5 ]ÁH 2 O were heated with molten NH 4 HF 2 at 473 K for $1 h in a platinum melting pot. The treatment of the precursor in these aggressive conditions indicates the high thermal stability of the trans-[RuNO(NH 3 ) 4 F] 2+ cation.…”
Section: Synthesis and Structural Descriptionmentioning
confidence: 99%