Skip to main content
Article
Localizing Perturbations of the Racemic Equilibria Involving Dipicolinate-Derived Lanthanide(III) Complexes
Chirality (2016)
  • Brian T. Nguyen, San Jose State University
  • Andrew J. Ingram, Stanford University
  • Gilles Muller, San Jose State University
Abstract
Helical D3 tris(4-amino-2,6-pyridine-dicarboxylate)terbium(III) and europium(III) complexes, which form a racemic equilibrium in aqueous solution, were prepared to study their secondary coordination sphere interactions with chiral amino acids. These interactions were probed using a combination of circularly polarized luminescence (CPL) and 13C NMR spectroscopy. The results indicate that, regardless of the interaction between the chiral molecule and the complex, without an accessible hydrogen-bond donor on the associating molecule, perturbation of the racemic equilibrium cannot occur. A generalized conclusion is established that indicates that the mechanism of chiral recognition by tris(dipicolinate)lanthanide(III) complexes is similar across a variety of analogous ligands. Chirality 28:325–331, 2016. © 2016 Wiley Periodicals, Inc.
Disciplines
Publication Date
2016
DOI
10.1002/chir.22584
Citation Information
Brian T. Nguyen, Andrew J. Ingram and Gilles Muller. "Localizing Perturbations of the Racemic Equilibria Involving Dipicolinate-Derived Lanthanide(III) Complexes" Chirality Vol. 28 Iss. 4 (2016) p. 325 - 331
Available at: http://works.bepress.com/gilles_muller/62/