期刊
COMPUTATIONAL AND THEORETICAL CHEMISTRY
卷 1204, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.comptc.2021.113423
关键词
Copper sensor; Vinyl-Ferrocenyl; DFT; Binding energy; Charge-transfer
资金
- Fondo Nacional de Ciencia y Tecnologia (FONDECYT-ANID, Chile) [1181582]
The selectivity of (FcL) ligand towards different cations was studied, showing strong charge transfer towards the copper cation. In most complexes, ligand to cation charge transfer was observed, with iron acting as the main electron donor. An exception was found where the organic moiety acted as the electron donor, allowing a bimetallic interaction.
The selectivity of (E)-2-[(3-(2-ferrocenyl)vinyl)-5,5-dimethylcyclohex-2-enylidenelmalononitrile (FcL) toward different cations was studied theoretically at the DFT level. Ten interaction sites were evaluated, and its energetic and electronic properties analyzed. Ligand to cation charge transfer was obtained in most of the studied complexes, iron acting as the main electron donor. An exception was observed, in which the organic moiety acted as electron donor and both, Fe and cation as acceptors, allowing a bimetallic interaction. The high selectivity of (FcL) ligand towards copper was stablished based on the number of formed complexes, the highest binding energy, and the strong charge transfer towards copper cation.
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