## Abstract ^1^H, ^13^C and ^15^N NMR studies of iron(II), ruthenium(II) and osmium(II) bis‐chelated cationic complexes with 2,2′:6′,2″‐terpyridine ([M(terpy)~2~]^2+^; M = Fe, Ru, Os) were performed. Significant shielding of nitrogen‐adjacent H(6) and deshielding of H(3′), H(4′) protons were observ
1H NMR assignment corrections and 1H, 13C, 15N NMR coordination shifts structural correlations in Fe(II), Ru(II) and Os(II) cationic complexes with 2,2′-bipyridine and 1,10-phenanthroline
✍ Scribed by Leszek Pazderski; Tomasz Pawlak; Jerzy Sitkowski; Lech Kozerski; Edward Szłyk
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 190 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.2600
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✦ Synopsis
Abstract
^1^H, ^13^C and ^15^N NMR studies of iron(II), ruthenium(II) and osmium(II) tris‐chelated cationic complexes with 2,2′‐bipyridine and 1,10‐phenanthroline of the general formula [M(LL)~3~]^2+^ (M = Fe, Ru, Os; LL = bpy, phen) were performed. Inconsistent literature ^1^H signal assignments were corrected. Significant shielding of nitrogen‐adjacent protons [H(6) in bpy, H(2) in phen] and metal‐bonded nitrogens was observed, being enhanced in the series Ru(II) → Os(II) → Fe(II) for ^1^H, Fe(II) → Ru(II) → Os(II) for ^15^N and bpy → phen for both nuclei. The carbons are deshielded, the effect increasing in the order Ru(II) → Os(II) → Fe(II). Copyright © 2010 John Wiley & Sons, Ltd.
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## 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
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