4.8 Article

A Redox-Active Bridging Ligand to Promote Spin Delocalization, High-Spin Complexes, and Magnetic Multi-Switchability

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 57, 期 26, 页码 7841-7845

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201803842

关键词

molecular magnetism; multiswitchability; non-innocent ligands; radicals; spin delocalization

资金

  1. ANR [ANR-16-CE29-0001-01]
  2. University of Bordeaux
  3. Region Nouvelle Aquitaine
  4. CNRS
  5. MOLSPIN COST action [CA15128]
  6. CSC
  7. EPSRC [EP/N006895/1]
  8. University of Southampton
  9. RSC
  10. IRIDIS High Performance Computing Facility

向作者/读者索取更多资源

A dinuclear Co-II complex, [Co-2(tphz)(tpy)(2)](n+) (n = 4, 3 or 2; tphz: tetrapyridophenazine; tpy: terpyridine), has been assembled using the redox-active and strongly complexing tphz bridging ligand. The magnetic properties of this complex can be tuned from spin-crossover with T-1/2 approximate to 470 K for the pristine compound (n = 4) to single-molecule magnet with an S-T= 5/2 spin ground state when once reduced (n = 3) to finally a diamagnetic species when twice reduced (n = 2). The two successive and reversible reductions are concomitant with an increase of the spin delocalization within the complex, promoting remarkably large magnetic exchange couplings and high-spin species even at room temperature.

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