TY - JOUR
T1 - Directional Electron Transfer in Crystals of [CrCo] Dinuclear Complexes Achieved by Chirality-Assisted Preparative Method
AU - Kanegawa, Shinji
AU - Shiota, Yoshihito
AU - Kang, Soonchul
AU - Takahashi, Kazuyuki
AU - Okajima, Hajime
AU - Sakamoto, Akira
AU - Iwata, Tatsuya
AU - Kandori, Hideki
AU - Yoshizawa, Kazunari
AU - Sato, Osamu
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/11/2
Y1 - 2016/11/2
N2 - The polarization switching mechanism is used in various devices such as pyroelectric sensors and memory devices. The change in polarization mostly occurs by ion displacement. The development of materials whose polarization switches via electron transfer in order to enhance operation speed is a challenge. We devised a synthetic and crystal engineering strategy that enables the selective synthesis of a [CrCo] heterometallic dinuclear complex with a polar crystal structure, wherein polarization changes stem from intramolecular charge transfer between Co and the ligand. Polarization can be modulated both by visible-light irradiation and temperature change. The introduction of chiral ligands was paramount to the successful polarization switching in the valence tautomeric compound. Mixing Cr and Co complexes with enantiopure chiral ligands resulted in the selective formation of only pseudosymmetric [CrCo] heterometallic complexes. Furthermore, the left-handed chiral ligands preferentially interacted with their right-handed counterparts, enabling molecules to form a polar crystal structure.
AB - The polarization switching mechanism is used in various devices such as pyroelectric sensors and memory devices. The change in polarization mostly occurs by ion displacement. The development of materials whose polarization switches via electron transfer in order to enhance operation speed is a challenge. We devised a synthetic and crystal engineering strategy that enables the selective synthesis of a [CrCo] heterometallic dinuclear complex with a polar crystal structure, wherein polarization changes stem from intramolecular charge transfer between Co and the ligand. Polarization can be modulated both by visible-light irradiation and temperature change. The introduction of chiral ligands was paramount to the successful polarization switching in the valence tautomeric compound. Mixing Cr and Co complexes with enantiopure chiral ligands resulted in the selective formation of only pseudosymmetric [CrCo] heterometallic complexes. Furthermore, the left-handed chiral ligands preferentially interacted with their right-handed counterparts, enabling molecules to form a polar crystal structure.
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U2 - 10.1021/jacs.6b05089
DO - 10.1021/jacs.6b05089
M3 - Article
AN - SCOPUS:84994259536
SN - 0002-7863
VL - 138
SP - 14170
EP - 14173
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 43
ER -