## Abstract ^1^H, ^13^C, ^195^Pt and ^15^N NMR studies of platinide(II) (M = Pd, Pt) chloride complexes with such alkyl and aryl derivatives of 2,2′‐bipyridine and 1,10‐phenanthroline as LL = 6,6′‐dimethyl‐bpy, 5,5′‐dimethyl‐bpy, 4,4′‐di‐__tert__‐butyl‐bpy, 2,9‐dimethyl‐phen, 2,9‐dimethyl‐4,7‐diphe
Luminescent metal complexes. 4—13C NMR spectra of the tris chelates of substituted 2,2′-bipyridyls and 1,10-phenanthrolines with ruthenium(II) and osmium(II)
✍ Scribed by Michael J. Cook; Anthony P. Lewis; Glenn S. G. McAuliffe
- Publisher
- John Wiley and Sons
- Year
- 1984
- Tongue
- English
- Weight
- 598 KB
- Volume
- 22
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
C Chemical shifts are reported for the ruthenium(II) tris complexes of thirteen 2,Z-bipyridyls and three 1,lO-phenanthrolines and for the osmium(]") bris complexes of five 2,2'-bpyridyls. Chelation induced shifts -&3 are discussed in terms of models for n back-bonding. -C NMR is shown to be a convenient tool for the direct observation of the geometrical isomerism of complexes formed from monosubstituted 13
📜 SIMILAR VOLUMES
## Abstract ^1^H, ^13^C and ^15^N NMR studies of platinide(II) (M = Pd, Pt) chloride complexes with methyl and phenyl derivatives of 2,2′‐bipyridine and 1,10‐phenanthroline [LL = 4,4′‐dimethyl‐2,2′‐bipyridine (dmbpy); 4,4′‐diphenyl‐2,2′‐bipyridine (dpbpy); 4,7‐dimethyl‐1,10‐phenanthroline (dmphen);
Chiral synthons containing either 13Cor 15N-labelled glycine were prepared. The 13C and 15N NMR spectra of the Ni(II) complex of the Schi † base of (S)-2-(N-benzylprolyl)aminobenzophenone and 13C-1-, 13C-2or 15N-labelled glycine were measured and assigned. The observed splitting of the carbon signal