Synthesis, mixed-spin-state structure and Langmuir-Blodgett deposition of amphiphilic Fe(iii) quinolylsalicylaldiminate complexes.

Designing and integrating Fe(iii)-based spin crossover (SCO) complexes onto substrates remains a challenging goal with only a handful of examples reported. In this work, we successfully synthesized and characterized three [Fe(qsal-OR)2]NO3 (qsal-OR = 5-alkoxy-2-[(8-quinolylimino)methyl]phenolate) complexes, in which R = C12H251, C16H332, and C22H453 to explore the impact of alkyl chain on the modulation of SCO activity and potential for self-assembly on a glass surface. The SCO is found to be gradual and incomplete in all cases, with the LS state more stabilised as the alkyl group shortens. We also demonstrate that all complexes form stable Langmuir films and achieve good transfer ratios to the glass surface, with 2 being the best in terms of stability. This paves the way for the SCO modulation of complexes in this class and the development of SCO devices.

The First Observation of Hidden Hysteresis in an Iron(III) Spin-Crossover Complex.

Molecular magnetic switches are expected to form the functional components of future nanodevices. Herein we combine detailed (photo-) crystallography and magnetic studies to reveal the unusual switching properties of an iron(III) complex, between low (LS) and high (HS) spin states. On cooling, it exhibits a partial thermal conversion associated with a reconstructive phase transition from a [HS-HS] to a [LS-HS] phase with a hysteresis of 25 K. Photoexcitation at low temperature allows access to a [LS-LS] phase, never observed at thermal equilibrium. As well as reporting the first iron(III) spin crossover complex to exhibit reverse-LIESST (light-induced excited spin state trapping), we also reveal a hidden hysteresis of 30 K between the hidden [LS-LS] and [HS-LS] phases. Moreover, we demonstrate that FeIII spin-crossover (SCO) complexes can be just as effective as FeII systems, and with the advantage of being air-stable, they are ideally suited for use in molecular electronics.

Solvatomorphism and anion effects in predominantly low spin iron(iii) Schiff base complexes.

A series of iron(iii) complexes [Fe(naphEen)2]X·sol (naphEen = 1-{[2-(ethylamino)-ethylimino]methyl}-2-naphtholate; X = F, sol = 0.5CH2Cl2·H2O 1; sol = H2O, X = Cl, 2 and X = Br 3) and [Fe(naphEen)2]I 4 has been prepared. The UV-Vis spectra reveal clear differences for 1 which DFT/TDDFT calculations suggest are due to an equilibrium between [Fe(naphEen)2]F and [Fe(naphEen)2F], the latter having a coordinated F ligand. The X-ray crystal structures of 2-4 show LS Fe(iii) centres in all cases and extensive aryl interactions that link the Fe centres into supramolecular squares. In 3 at room temperature the compound loses half an equivalent of water resulting in a change in space group from Monoclinic P21/n to C2/c. Magnetic studies indicate that 1 is trapped in a mixed spin state being ca. 40% HS while 2-4 are effectively low spin up to 350 K. In contrast, Mössbauer spectroscopic studies of 1 indicate a gradual but incomplete spin crossover. The magnetic properties of 2-4 contrast with the related [Fe(salEen-X)2]anion derivatives which are often spin crossover active.