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Heteroleptic iron(II) spin-crossover complexes based on a 2,6-Bis(pyrazol-1-yl)pyridine-type ligand functionalized with a carboxylic acid
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Two new heteroleptic complexes [Fe(1bppCOOH)(3bpp-bph)](ClO4)2·solv (1·solv, solv = various solvents; 1bppCOOH = 2,6-bis(1H-pyrazol-1-yl)isonicotinic acid; 3bpp-bph = 2,6-bis(5-([1,1′-biphenyl]-4-yl)-1H-pyrazol-3-yl)pyridine) and [Fe(1bppCOOH)(1bppCOOEt)](ClO4)2·0.5Me2CO (2·0.5Me2CO, 1bppCOOEt = ethyl 2,6-bis(1H-pyrazol-1-yl)isonicotinate) were designed and prepared. The heteroleptic compound 1·solv was obtained by the combination of stoichiometric amounts of Fe(ClO4)2, 1bppCOOH, and 3bpp-bph, and it was designed to fine-tune the spin crossover (SCO) properties with respect to the previously reported homoleptic compound [Fe(1bppCOOH)2](ClO4)2. Indeed, the introduction of a new substituted 3bpp ligand induces a weaker ligand field in addition to promoting the formation of π···π and C-H···π intermolecular interactions through the biphenyl groups. For the desolvated counterpart 1, this results in a shift of the SCO curve toward room temperature and the observation of a 13 K hysteresis width. Besides, compound 2·0.5Me2CO, which represents the first example of a heteroleptic complex containing two 1bpp tridentate ligands, stabilizes the LS state at room temperature confirming the same trend observed for the corresponding homoleptic compounds. Interestingly, both 1 and 2·0.5Me2CO heteroleptic complexes exhibit photoswitchable properties when irradiating with a 523 nm laser at 10 K. Preliminary characterization of the deposited complexes on native SiO2 by X-ray absorption measurements suggests oxidation and decomposition of the complexes.
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GARCÍA-LÓPEZ, Victor, PALACIOS-CORELLA, Mario, GIRONÉS-PÉREZ, Verónica, BARTUAL-MURGUI, Carlos, REAL, José antonio, PELLEGRIN, Eric, HERRERO-MARTIN, Javier, AROMÍ BEDMAR, Guillem, CLEMENTE-LEON, Miguel, CORONADO, Eugenio. Heteroleptic iron(II) spin-crossover complexes based on a 2,6-Bis(pyrazol-1-yl)pyridine-type ligand functionalized with a carboxylic acid. _Inorganic Chemistry_. 2019. Vol. 58, núm. 18, pàgs. 12199-12208. [consulta: 28 de gener de 2026]. ISSN: 0020-1669. [Disponible a: https://hdl.handle.net/2445/154177]