The effect of oxidation state and tert-butyl substituents on the thermal behavior and thin-film morphology of cobalt-complexes (FK 102 and FK 209)

• Type: Article in International Scientific Journal
• Date: 2022

Authors

Costa, JCS (Author) FCUP; Carvalho, RM (Author) Other; Silva, RMA (Author) Other; Ana I M C L Lobo Ferreira (Author) FCUP; Luis M N B F Santos (Author) FCUP

Journal

Title: Journal of Chemical Thermodynamics

Vol. 174

ISSN: 0021-9614

Publisher: Elsevier

Indexing

Scopus - 1 Citation

Other information

Authenticus ID: P-00W-V1G

DOI: 10.1016/j.jct.2022.106856

Abstract (EN): This work reports the thermodynamic and morphological study and characterization of four salts consisting of a divalent/trivalent cobalt complex with pyrazole-pyridine ligands (FK 102 and FK 209 samples) and bis(trifluoromethylsulfonyl)imide (TFSI) moieties as counter anions. The oxidation state of the central metal (Co(II) or Co(III)) and the presence of tert-butyl (t-Bu) groups in the ligand structure were found to have a strong impact on the thermal behavior, phase stability, heat capacities, and thin-film morphology of each salt. The Co(II) complexes exhibited good thermal stability up to 600 K. Lower thermal stability was observed for the Co(III) congeners. The FK 209 Co(III) displayed a higher melting temperature but a partial decomposition during or above melting was detected. The higher melting temperatures observed for the Co(III) complexes were found to be entropically driven. However, the addition of t-Bu in the ligand (FK 209) leads to an increase in the melting temperature, which is driven by the enthalpy of fusion. The four compounds studied evidenced a large glass-forming ability. Moreover, the thermal stability of the glassy state was clearly increased when the ligands comprised t-Bu groups. The contribution of the t-Bu group for the molar heat capacity in the solid phase, at T = 298.15 K, was found to be (110 ± 3) J·K¿1·mol¿1 and (98 ± 4) J·K¿1·mol¿1 for the Co(II) and Co(III) complexes, respectively. These results are in good agreement with the contribution of the t-Bu group observed for both solid and liquid phases in other materials, indicating that the t-Bu groups are relatively unhindered in the crystalline phase of the salts. The morphological behavior of the thin films of FK 102 samples was found to be quite similar to the observed for typical ionic liquids, with the formation of micro- and nanodroplets onto different substrates. The introduction of t-Bu substituents in the ligand structure was found to have a strong impact on the formation of homogeneous and compact nanofilms for the FK 209 salts. © 2022 Elsevier Ltd

Language: English

Type (Professor's evaluation): Scientific