Insights into electronic and structural properties of novel Pd(II) salen-type complexes

Autor: Cristina Freire, J. R. Fonseca, Alexandre L. Magalhães, M. Teresa Duarte, Javier Martinez, Luís Cunha-Silva
Rok vydání: 2010
Předmět:
Zdroj: Inorganica Chimica Acta. 363:4096-4107
ISSN: 0020-1693
DOI: 10.1016/j.ica.2010.08.023
Popis: Novel palladium(II) complexes with salen-type ligands based on 3-methylsalicyladehyde and a set of aliphatic diamines (C1 to C4) have been synthesised and characterized by spectroscopic techniques (UV-Vis and FTIR), Density Functional Theory (DFT) calculations and single-crystal X-ray diffraction for C1 and C4. X-ray diffraction analysis of these complexes was focused on coordination sphere and supramolecular arrangements. In the two compounds, the molecules form dimers, being the most relevant intermolecular interactions the hydrogen bonds of the type C-H···O, C-H···π and π···π stacking interactions between the six-membered metallocycles. Electronic spectra of all Pd(II) complexes are dominated by charge transfer and intraligand bands at λ < 400 nm. DFT calculations showed that the HOMO is ligand-dominated, with the metal contribution being ~18% for all complexes. This suggests that the structural/electronic differences between the ligands do not influence significantly the participation of metal orbitals in HOMO. All the complexes exhibit dipole moments with the same direction, from the aldehyde moiety towards the imine bridge with C2 and C3 showing quite similar values, μ C2 = 5.49 and μ C3 = 5.54 D, whereas complexes C1 and C4 show slightly higher values: μ C1 = 5.79 and μ C4 = 6.17 D. The magnitude of bond lengths and angles predicted by DFT calculations are comparable to those determined by X-ray crystallography. The experimental vibrational frequencies of the Pd(II) complexes were correlated with the values estimated by DFT calculations. The good agreement between the experimental and theoretical vibrational data allowed the assignment of relevant IR bands to molecular vibration modes.
Databáze: OpenAIRE
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