Crystal design of monometallic single-molecule magnets consisting of cobalt-aminoxyl heterospins

Shinji Kanegawa, Satoru Karasawa, Masataka Maeyama, Motohiro Nakano, Noboru Koga

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91 Citations (Scopus)


Five N-aryl-N-pyridylaminoxyls, which have no substituent (PhNOpy), one substituent (MeOPh-NOpy and tert-BuPhNOpy) at the 4-position, and three substituents (TPPNOpy and TBPNOpy) at the 2, 4, and 6-positions of the phenyl ring, were prepared as new ligands for cobalt-aminoxyl heterospin systems. The 1:4 complexes, [Co(NCS)2(PhNOpy)4] (1), [Co(NCS) 2(MeOPhNOpy)4] (2), [Co(NCS)2(tertBuPhNOpy) 4] (3), [Co(NCS)2(TPPNOpy)4] (4), [Co(NCS) 2(TBPNOpy)4] (5a), and [Co(NCO)2(TBPNOpy) 4] (5b), were obtained as single crystals. The molecular geometry revealed by X-ray crystallography for all complexes except 4 is a compressed octahedron. In the crystal structure of 1, 2, and 3, the organic spin centers have various short contacts within 4 Å with the neighboring molecules to form 3D and 2D spin networks. On the other hand, complexes 5a and 5b have no significant short intermolecular contacts, indicating that they are magnetically isolated. 1 and 2 behaved as a 3D antiferromagnet with a Neel temperature, TN, of 22 K and as a weak 3D antiferromagnet with a TN of 2.9 K and a spin-flop field at 1.9 K, Hsp(1.9), of 0.7 kOe, respectively. 3 was a canted 2D antiferromagnet (a weak ferromagnet) with T N = 4.8 K and showed a hysteresis loop with a coercive force, H c, of 1.3 kOe at 1.9 K. On the other hand, the trisubstituted complexes 4, 5a, and 5b functioned as single-molecule magnets (SMMs). 5b had an effective activation barrier, Ueff, value of 28 K in a microcrystalline state and 48 K in a frozen solution.

Original languageEnglish
Pages (from-to)3079-3094
Number of pages16
JournalJournal of the American Chemical Society
Issue number10
Publication statusPublished - Mar 12 2008

All Science Journal Classification (ASJC) codes

  • Catalysis
  • General Chemistry
  • Biochemistry
  • Colloid and Surface Chemistry


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