Understanding M-ligand bonding and mer-/fac-isomerism in tris(8-hydroxyquinolinate) metallic complexes

• Type: Article in International Scientific Journal
• Date: 2016

Authors

Carlos F. R. A. C. Lima (Author) Other; Ricardo J. S. Taveira (Author) Other; José C. S. Costa (Author) FEUP; Ana M. Fernandes (Author) Other; André Melo (Author) Other; Artur M. S. Silva (Author) Other; Luís M. N. B. F. Santos (Author) Other

Journal

Title: Physical Chemistry Chemical Physics

Vol. 18 No. 24

Pages: 16555-16565

ISSN: 1463-9076

Publisher: Royal Society of Chemistry

Indexing

ISI Web of Knowledge - 21 Citations

Scopus - 23 Citations

INSPEC

Associated Projects

LEPABE - Laboratório de Engenharia de Processos, Ambiente, Biotecnologia e Energia

Other information

Authenticus ID: P-00K-JT7

DOI: 10.1039/C6CP02608G

Abstract (EN): Tris(8-hydroxyquinolinate) metallic complexes, Mq3, are one of the most important classes of organic semiconductor materials. Herein, the nature of the chemical bond in Mq3 complexes and its implications on their molecular properties were investigated by a combined experimental and computational approach. Various Mq3 complexes, resulting from the alteration of the metal and substitution of the 8-hydroxyquinoline ligand in different positions, were prepared. The mer-/fac-isomerism in Mq3 was explored by FTIR and NMR spectroscopy, evidencing that, irrespective of the substituent, mer- and fac-are the most stable molecular configurations of Al(III) and In(III) complexes, respectively. The relative M–ligand bond dissociation energies were evaluated experimentally by electrospray ionization tandem mass spectrometry (ESI-MS-MS), showing a non-monotonous variation along the group (Al 4 In 4 Ga). The results reveal a strong covalent character in M–ligand bonding, which allows for through-ligand electron delocalization, and explain the preferred molecular structures of Mq3 complexes as resulting from the interplay between bonding and steric factors. The mer-isomer reduces intraligand repulsions, being preferred for smaller metals, while the fac-isomer is favoured for larger metals where stronger covalent M–ligand bonds can be formed due to more extensive through-ligand conjugation mediated by metal ‘‘d’’ orbitals.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 11