Pressure induced enhancement of the magnetic ordering temperature in rhenium(IV) monomers

Christopher H. Woodall, Gavin A. Craig, Alessandro Prescimone, Martin Misek, Joan Cano, Juan Faus, Michael R. Probert, Simon Parsons, Stephen Moggach, José Martínez-lillo, Mark Murrie, Konstantin V. Kamenev, Euan K. Brechin

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Materials that demonstrate long-range magnetic order are synonymous with information storage and the electronics industry, with the phenomenon commonly associated with metals, metal alloys or metal oxides and sulfides. A lesser known family of magnetically ordered complexes are the monometallic compounds of highly anisotropic d-block transition metals; the ‘transformation’ from isolated zero-dimensional molecule to ordered, spin-canted, three-dimensional lattice being the result of through-space interactions arising from the combination of large magnetic anisotropy and spin-delocalization from metal to ligand which induces important intermolecular contacts. Here we report the effect of pressure on two such mononuclear rhenium(IV) compounds that exhibit long-range magnetic order under ambient conditions via a spin canting mechanism, with Tc controlled by the strength of the intermolecular interactions. As these are determined by intermolecular distance, ‘squeezing’ the molecules closer together generates remarkable enhancements in ordering temperatures, with a linear dependence of Tc with pressure.
Original languageEnglish
Article number13870
Number of pages7
JournalNature Communications
Early online date21 Dec 2016
Publication statusPublished - 21 Dec 2016


Dive into the research topics of 'Pressure induced enhancement of the magnetic ordering temperature in rhenium(IV) monomers'. Together they form a unique fingerprint.

Cite this