A large dinuclear Fe(ii) triple helicate demonstrating a two-step spin crossover

2020 ◽  
Vol 56 (62) ◽  
pp. 8838-8841
Author(s):  
Kyle J. Howard-Smith ◽  
Alexander R. Craze ◽  
Hikaru Zenno ◽  
Junya Yagyu ◽  
Shinya Hayami ◽  
...  

The largest reported dinuclear Fe(ii) triple helicate system to exhibit spin crossover is presented, with exploration of the two-step spin-transition.

Crystals ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 376 ◽  
Author(s):  
Alexander Craze ◽  
Mohan Bhadbhade ◽  
Cameron Kepert ◽  
Leonard Lindoy ◽  
Christopher Marjo ◽  
...  

This work explores the effect of lattice solvent on the observed solid-state spin-transition of a previously reported dinuclear Fe(II) triple helicate series 1–3 of the general form [FeII2L3](BF4)4(CH3CN)n, where L is the Schiff base condensation product of imidazole-4-carbaldehyde with 4,4-diaminodiphenylmethane (L1), 4,4′-diaminodiphenyl sulfide (L2) and 4,4′-diaminodiphenyl ether (L3) respectively, and 1 is the complex when L = L1, 2 when L = L2 and 3 when L = L3 (Craze, A.R.; Sciortino, N.F.; Bhadbhade, M.M.; Kepert, C.J.; Marjo, C.E.; Li, F. Investigation of the Spin Crossover Properties of Three Dinuclear Fe(II) Triple Helicates by Variation of the Steric Nature of the Ligand Type. Inorganics. 2017, 5 (4), 62). Desolvation of 1 and 2 during measurement resulted not only in a decrease in T1/2 and completeness of spin-crossover (SCO) but also a change in the number of steps in the spin-profile. Compounds 1 and 2 were observed to change from a two-step 70% complete transition when fully solvated, to a single-step half complete transition upon desolvation. The average T1/2 value of the two-steps in the solvated materials was equivalent to the single T1/2 of the desolvated sample. Upon solvent loss, the magnetic profile of 3 experienced a transformation from a gradual SCO or weak antiferromagnetic interaction to a single half-complete spin-transition. Variable temperature single-crystal structures are presented and the effects of solvent molecules are also explored crystallographically and via a Hirshfeld surface analysis. The spin-transition profiles of 1–3 may provide further insight into previous discrepancies in dinuclear triple helicate SCO research reported by the laboratories of Hannon and Gütlich on analogous systems (Tuna, F.; Lees, M. R.; Clarkson, G. J.; Hannon, M. J. Readily Prepared Metallo-Supramolecular Triple Helicates Designed to Exhibit Spin-Crossover Behaviour. Chem. Eur. J. 2004, 10, 5737–5750 and Garcia, Y.; Grunert, C. M.; Reiman, S.; van Campenhoudt, O.; Gütlich, P. The Two-Step Spin Conversion in a Supramolecular Triple Helicate Dinuclear Iron(II) Complex Studied by Mössbauer Spectroscopy. Eur. J. Inorg. Chem. 2006, 3333–3339).


2019 ◽  
Vol 48 (41) ◽  
pp. 15515-15520 ◽  
Author(s):  
Sharon E. Lazaro ◽  
Adil Alkaş ◽  
Seok J. Lee ◽  
Shane G. Telfer ◽  
Keith S. Murray ◽  
...  

Two iron(iii) complexes, [Fe(qsal-X)2]OTs·nH2O, are found to exhibit abrupt spin crossover with the spin transition temperature substituent dependent, and X⋯O halogen bonds linking the spin centres.


Author(s):  
Alexander R. Craze ◽  
Hikaru Zenno ◽  
Michael C. Pfrunder ◽  
John C. McMurtrie ◽  
Shinya Hayami ◽  
...  

Author(s):  
Nikita Konstantinov ◽  
Arthur Tauzin ◽  
Ulrich Nguetchuissi Noumbé ◽  
Diana Dragoe ◽  
Bohdan Kundys ◽  
...  

An opto-electronic switching device made from an evaporated spin crossover thin film over a graphene sensor is presented. The electrical transduction of both temperature and light-induced reversible spin transitions are demonstrated.


2013 ◽  
Vol 42 (28) ◽  
pp. 10144 ◽  
Author(s):  
Guo-Ping Shen ◽  
Li Qi ◽  
Lei Wang ◽  
Yan Xu ◽  
Jing-Jing Jiang ◽  
...  

2016 ◽  
Vol 45 (28) ◽  
pp. 11267-11271 ◽  
Author(s):  
F. Pointillart ◽  
X. Liu ◽  
M. Kepenekian ◽  
B. Le Guennic ◽  
S. Golhen ◽  
...  

A thermal and photo-induced spin transition in a tetrathiafulvalene-based Fe(ii) complex.


2015 ◽  
Vol 54 (11) ◽  
pp. 5145-5147 ◽  
Author(s):  
Jie Luan ◽  
Jian Zhou ◽  
Zhan Liu ◽  
Bowen Zhu ◽  
Huisi Wang ◽  
...  

2019 ◽  
Author(s):  
Tim Stauch ◽  
Romit Chakraborty ◽  
Martin Head-Gordon

Spin state switching on external stimuli is a phenomenon with wide applicability ranging from molecular electronics to gas activation in nanoporous frameworks. Here we model spin crossover as a function of hydrostatic pressure in octahedrally coordinated transition metal centers by applying a field of effective nuclear forces that compress the molecule towards its centroid. For spin crossover in first-row transition metals coordinated by hydrogen, nitrogen, and carbon monoxide, we find the pressure required for spin transition to be a function of ligand position in the spectrochemical sequence. While pressures on the order of 1 GPa are required to flip spins in homogeneously ligated octahedral sites, we demonstrate a five-fold decrease in spin transition pressure for the archetypal strong field ligand carbon monoxide in octahedrally coordinated Fe<sup>2+</sup> in [Fe(II)(NH<sub>3</sub>)<sub>5</sub>CO]<sup>2+</sup>.


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