posted on 2018-12-04, 12:54authored byIain Wright, Claire Wilson, Simon J. Coles, Peter J. Skabara
A series of three homoleptic, monoanionic gold dithiolene complexes of oligothiophene ligands which coordinate via a central thiophene-3,4-dithiolate chelate are presented. The oligomer chains are three, five and seven thiophenes long and the complexes display hybrid optoelectronic properties featuring characteristics of both the oligothiophene chains and the delocalised metal dithiolene centre. The properties of the complexes have been characterised using a variety of spectroscopic and electrochemical methods complemented by computational studies. Solid state spectroelectrochemistry has revealed that upon oxidation these complexes display intense and broad absorption across the visible spectrum. In attempting to produce nickel analogues of these materials a single crystal of a photo-oxidised nickel dithiolene complex has also been isolated.
Funding
PJS and IAW acknowledge the EPSRC for funding. IAW acknowledges Loughborough University and the Royal Society of Chemistry Research Fund (Grant No. RF18-5353) for funding.
History
School
Science
Department
Chemistry
Published in
Dalton Transactions
Citation
WRIGHT, I.A. ... et al, 2018. Broadband near-IR absorbing Au-dithiolene complexes bearing redox-active oligothiophene ligands. Dalton Transactions, 48, pp. 107-116.
This work is made available according to the conditions of the Creative Commons Attribution 3.0 Unported (CC BY 3.0) licence. Full details of this licence are available at: http://creativecommons.org/licenses/by/3.0/
Acceptance date
2018-11-15
Publication date
2018-11-16
Notes
This is an Open Access Article. It is published by The Royal Society of Chemistry under the Creative Commons Attribution 3.0 Unported Licence (CC BY 3.0). Full details of this licence are available at: https://creativecommons.org/licenses/by/3.0/