Controlling the chirality of metal complexes or supramolecular assemblies continues to be a challenging and fascinating area of research. [1] The chirality of these systems may be related, for example, to the spatial disposition of chelating ligands around a metal ion, [1a] to the formation of doubl
Helicity Inversion in Lanthanide(III) Complexes with Chiral Nonaaza Macrocyclic Ligands
✍ Scribed by Janusz Gregoliński; Jerzy Lisowski
- Publisher
- John Wiley and Sons
- Year
- 2008
- Tongue
- English
- Weight
- 149 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
✦ Synopsis
In this communication, the temperature used in monitoring the conversion of the M diastereomer into the P diasteromer was incorrectly quoted. On page 6124, right column, lines 11-12 from the top, it should read "After heating at 318 K", similarly in the caption to Figure 3 on the same page it should read "after heating in water solution at 318 K".
📜 SIMILAR VOLUMES
## Abstract Lanthanide complexes of a hexaaza macrocyclic ligand containing a pyridine head unit (L) were synthesized (Ln = La–Lu, except Pm). The solid‐state structures of the corresponding La, Ce, Pr, Nd, and Lu complexes were determined by single‐crystal X‐ray crystallography, and they reveal th