Literature DB >> 32812653

A Reversible Hydrogen-Bond Isomerization Triggered by an Abrupt Spin Crossover near Room Temperature.

Verónica Jornet-Mollá1, Carlos Giménez-Saiz1, Dmitry S Yufit2, Judith A K Howard2, Francisco M Romero1.   

Abstract

The spin crossover salt [Fe(bpp)2 ](isonicNO)2 ⋅ 2.4 H2 O (1⋅2.4 H2 O) (bpp=2,6-bis(pyrazol-3-yl)pyridine; isonicNO=isonicotinate N-oxide anion) exhibits a very abrupt spin crossover at T1/2 =274.4 K. This triggers a supramolecular linkage (H-bond) isomerization that responds reversibly towards light irradiation or temperature change. Isotopic effects in the thermomagnetic behavior reveal the importance of hydrogen bonds in defining the magnetic state. Further, the title compound can be reversibly dehydrated to afford 1, a material that also exhibits spin crossover coupled to H-bond isomerization, leading to strong kinetic effects in the thermomagnetic properties.
© 2020 Wiley-VCH GmbH.

Entities:  

Keywords:  hydrogen bonds; iron(II) complexes; isomerization; solvent exchange; spin crossover

Year:  2020        PMID: 32812653     DOI: 10.1002/chem.202003654

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  1 in total

1.  Co-crystallisation as a modular approach to the discovery of spin-crossover materials.

Authors:  Lee T Birchall; Giada Truccolo; Lewis Jackson; Helena J Shepherd
Journal:  Chem Sci       Date:  2022-02-18       Impact factor: 9.825

  1 in total

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