posted on 2020-06-22, 19:34authored bySheng-Qun Su, Shu-Qi Wu, Michael L. Baker, Peter Bencok, Nobuaki Azuma, Yuji Miyazaki, Motohiro Nakano, Soonchul Kang, Yoshihito Shiota, Kazunari Yoshizawa, Shinji Kanegawa, Osamu Sato
Orbital angular momentum
plays a vital role in various applications,
especially magnetic and spintronic properties. Therefore, controlling
orbital angular momentum is of paramount importance to both fundamental
science and new technological applications. Many attempts have been
made to modulate the ligand-field-induced quenching effects of orbital
angular momentum to manipulate magnetic properties. However, to date,
reported changes in the magnitude of orbital angular momentum are
small in both molecular and solid-state magnetic materials. Moreover,
no effective methods currently exist to modulate orbital angular momentum.
Here we report a dynamic bond approach to realize a large change in
orbital angular momentum. We have developed a Co(II) complex that
exhibits coordination number switching between six and seven. This
cooperative dynamic bond switching induces considerable modulation
of the ligand field, thereby leading to substantial quenching and
restoration of the orbital angular momentum. This switching mechanism
is entirely different from those of spin-crossover and valence tautomeric
compounds, which exhibit switching in spin multiplicity.