T. Ishikawa

TL;DR: Double-decker phthalocyanine complexes with Tb3+ or Dy3+ showed slow magnetization relaxation as a single-molecular property and a significant temperature rise results from a mechanism in the relaxation process different from that in the transition-metal-cluster SMMs.

TL;DR: In this article, an alternating current (ac) magnetic susceptibility and magnetization hysteresis loop measurements have been carried out for anionic bis(phthalocyaninato)terbium and bis (phthalocyclichenato)dysprosium and it has been found that the magnetization relaxation in the Tb complex is dominated by the two-phonon Orbach process in the temperature range 25−40 K and direct or Raman process below 25 K.

TL;DR: The observed photo-induced spectroscopic change shows that this photoinduced phase transition process is caused by the cooperative melting of charge ordering assisted by coherent phonon generation.

TL;DR: The ac susceptibility measurements on the complex with octa(dodecoxy)-substituted Pc ligand proved that the significant rise of the temperatures occurs as an intrinsic single-molecular property of the complex possessing both J = 6 and S = (1)/(2) systems, and is not due to long-range magnetic order or interactions between adjacent unpaired pi-electrons.

TL;DR: The ultrafast photoresponse of the molecular crystal Me4P[Pt(dmit)2]2 is reported, which exhibits a photoinduced charge transfer similar to transitions between thermally accessible states, and how femtosecond electron diffraction can be applied to directly observe the associated molecular motions.