Journal
DALTON TRANSACTIONS
Volume 47, Issue 2, Pages 491-506Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7dt02320k
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Funding
- DAAD
- Fonds der Chemischen Industrie
- Deutsche Forschungsgemeinschaft DFG [PE1513/4-1]
- Deutsche Forschungsgemeinschaft [SFB 658]
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A series of Fe2+ SCO complexes of substituted 2-(pyridin-2-yl)-1,10-phenanthrolines 2 was prepared and the SCO (spincrossover) properties were characterized in the solid state (X-ray crystallography, SQUID magnetometry) and in solution (VT-H-1 NMR spectroscopy), augmented by theoretical modelling. Bismeridional coordination of the tridendate 2a-c and tetradentate 2d ligands gives octahedral and distorted trigonal-dodecahedral complexes [Fe(2)(2)](2+), respectively, which were identified as SCO complexes with the transition temperature T-1/2 below room temperature. SCO in the solid state is limited to bromo-substituted [Fe(2a)(2)](2+) (Dalton Trans., 2017, 46, 6218-6229) and [Fe(2b)(2)](2+) with a pyridine-appended phenyl group, whereas solution state NMR studies reveal SCO behaviour for all complexes, which is in agreement with DFT derived results. As anticipated from its N6(+2) coordination in the HS state, DFT structure modelling of [Fe(2d)(2)](2+) identified deviation from a structure-conserving SCO reaction coordinate; that is, Fe-N breathing is accompanied by a change in the coordination number. Accordingly, a remarkably slow SCO is observed in [Fe(2d)(2)](2+), owing to an extended coordinate. De-novo defined characteristic temperatures T(tHSLS) are introduced as structure-dependent parameters deemed to define the onset of phenomenological slow SCO. The rich phenomenology of the NMR spectra of [Fe(2)(2)](2+) is identified to be largely controlled by the dynamics of spin-state exchange and a qualitative illustration of the NMR-reporters of SCO is suggested.
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