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Solid‐State and Solution Structure of Lanthanide(III) Complexes with a Flexible Py‐N 6 Macrocyclic Ligand
Author(s) -
Núñez Cristina,
MatoIglesias Marta,
Bastida Rufina,
Macías Alejandro,
PérezLourido Paulo,
PlatasIglesias Carlos,
Valencia Laura
Publication year - 2009
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200801088
Subject(s) - chemistry , lanthanide , denticity , crystallography , ligand (biochemistry) , crystal structure , metal , pyridine , density functional theory , ion , stereochemistry , computational chemistry , medicinal chemistry , organic chemistry , biochemistry , receptor
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 the presence of three different mononuclear complexes with three different conformations of the macrocycle and coordination environments around the metal ions. In all complexes the lanthanide ion is coordinated in an endomacrocyclic manner to the six nitrogen donor atoms of the ligand. In the La, Ce, and Pr complexes the metal ions show a 12‐coordinate mononuclear environment in which 3 nitrate anions coordinate in a bidentate fashion. However, in the Nd analogue the metal ion displays a 10‐coordinated environment with the coordination of 2 bidentate nitrate groups, whereas Lu shows a 9‐coordinate environment interacting with 2 nitrate ligands, one of them acting as bidentate and the second one coordinating in a monodentate fashion. The 1 H and 13 C NMR spectra of the complexes recorded in CD 3 CN suggest that the complexes adopt in solution a similar structure to that observed for the Nd complex in the solid state. The [Ln(L)(NO 3 ) 3 ] and [Ln(L)(NO 3 ) 2 ] + complexes were characterized by density functional theory (DFT) calculations (B3LYP model). The structures obtained from these calculations for La, Ce, Pr, and Nd are in good agreement with the experimental solid‐state structures. The relative stabilities of the [Ln(L)(NO 3 ) 2 ] + complexes with respect to the [Ln(L)(NO 3 ) 3 ] ones (Ln = La, Nd, Gd, Ho, or Lu) were studied both in vacuo and in acetonitrile solution (PCM model) at the same computational level. Our calculations indicate that in solution the [Ln(L)(NO 3 ) 2 ] + species is the most stable one along the whole lanthanide series, in agreement with the NMR spectroscopic data.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)