TY - JOUR
T1 - Rational Construction of Molecular Electron-Conducting Nanowires Encapsulated in a Proton-Conducting Matrix in a Charge Transfer Salt
AU - Donoshita, Masaki
AU - Yoshida, Yukihiro
AU - Maesato, Mitsuhiko
AU - Kitagawa, Hiroshi
N1 - Publisher Copyright:
© 2022 American Chemical Society.
PY - 2022/9/21
Y1 - 2022/9/21
N2 - Insulated molecular wires have gained significant attention owing to their potential contribution in the fields of nanoelectronics and low-dimensional chemistry/physics. Based on molecular charge transfer salts, we demonstrate, for the first time, the rational construction of molecular electron-conducting wires encapsulated in a proton-conducting matrix, which possibly paves the way to ionoelectronics. As expected from the molecular structure of the newly designed complex anion (i.e., propeller-shaped structure with hydrogen-bonding sites at four edges), a three-dimensional hydrogen-bonded framework was constructed within the crystal, which contains a one-dimensional array of an electron donor, tetrathiafulvalene (TTF). From the single-crystal crystallographic and spectroscopic studies, it was clarified that the nonstoichiometric deprotonation of anions and partial oxidation of TTFs occur, whereas the anion is electronically inert. Moderate conductivities of electron and proton were confirmed by dc and ac conductivity measurements. In addition, the electronic isolation of TTF wires was confirmed by the magnetic susceptibility data.
AB - Insulated molecular wires have gained significant attention owing to their potential contribution in the fields of nanoelectronics and low-dimensional chemistry/physics. Based on molecular charge transfer salts, we demonstrate, for the first time, the rational construction of molecular electron-conducting wires encapsulated in a proton-conducting matrix, which possibly paves the way to ionoelectronics. As expected from the molecular structure of the newly designed complex anion (i.e., propeller-shaped structure with hydrogen-bonding sites at four edges), a three-dimensional hydrogen-bonded framework was constructed within the crystal, which contains a one-dimensional array of an electron donor, tetrathiafulvalene (TTF). From the single-crystal crystallographic and spectroscopic studies, it was clarified that the nonstoichiometric deprotonation of anions and partial oxidation of TTFs occur, whereas the anion is electronically inert. Moderate conductivities of electron and proton were confirmed by dc and ac conductivity measurements. In addition, the electronic isolation of TTF wires was confirmed by the magnetic susceptibility data.
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U2 - 10.1021/jacs.2c07258
DO - 10.1021/jacs.2c07258
M3 - Article
C2 - 36074928
AN - SCOPUS:85137914509
SN - 0002-7863
VL - 144
SP - 17149
EP - 17155
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 37
ER -