The reactions of [N 3 P 3 (dobp) 2 Cl 2 ] and [N 3 P 3 (dobp)Cl 4 ] with revealed that the complexation of the N atom of one 4oxypyridine ligand by the W(CO) 5 fragment has a a mixture of HOC 5 H 4 N-4 and K 2 CO 3 in acetone give the cyclotriphosphazenes [N 3 P 3 (dobp) 2 (OC 5 H 4 N-4) 2 ] and [N
Multinuclear 195Pt and 15N magnetic resonance spectroscopic studies of the reaction of K[PtCl3(NH3)] with KI and amines
✍ Scribed by Y. Qu; N. Farrell; M. Valsecchi; L. de Greco; S. Spinelli
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 452 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
Reaction of the platinum complex K[PtCl~3~(NH~3~)] with NH~3~ or NH~2~(CH~2~)~n~NH~2~ in the presence of I^−^ gives the mixed chloroiodoamine complexes cis‐[PtCl~3~(NH~3~)~2~] and [{cis‐Pt(Cl)~3~(I)(NH~3~)~2~}~2~μNH~2~(CH~2~)~n~NH~2~], respectively. These findings prompted an examination of the nature of the reaction of K[PtCl~3~(NH~3~)] with I^−^ in detail. Rapid displacement of two chlorides to give the trans‐[Pt(I)~2~Cl(NH~3~)]^−^ anion is observed with a subsequent slow displacement of the third chloride to give the [PtI~3~(NH~3~)]^−^ anion. Concomitant with the formation of the triiodo anion, dimerization occurs, giving the iodo‐bridged compound [PtI~2~(NH~3~)]~2~. Correlation of δ(^195^Pt) and δ(^15^N) chemical shifts and ^1^J(^195^Pt,^15^N) coupling constants was made with literature values, allowing a complete set of data for the series [PtX~n~(NH~3~)~4 − n~]^(2 − n)+^ with systematic variation of X (Cl,I) to be presented.
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