TY - JOUR
T1 - Ferroelectric low-voltage ON/OFF switching of chiral benzene-1,3,5-tricarboxamide derivative
AU - Wu, Jianyun
AU - Takeda, Takashi
AU - Hoshino, Norihisa
AU - Akutagawa, Tomoyuki
N1 - Funding Information:
This work was supported by a Grant-in-Aid for Scientific Research on KAKENHI Kibankenkyu (A) (JP19H00886), KAKENHI (JP20H04655), JST CREST Grant Number JPMJCR18I4, and ‘‘Dynamic Alliance for Open Innovation Bridging Human, Environment and Materials’’ from MEXT.
Publisher Copyright:
© 2020 The Royal Society of Chemistry.
PY - 2020/8/14
Y1 - 2020/8/14
N2 - The phase transition behaviour, molecular assemblies, and dielectric responses of an N,N′,N′′-trialkylbenzene-1,3,5-tricarboxamide derivative bearing chiral (S)-3,7-dimethyloctyl chains (S-3BC) were compared with those of an N,N′,N′′-trioctadecylbenzene-1,3,5-tricarboxamide derivative (3BC) bearing achiral -CONHC14H29 chains. Chiral S-3BC showed a similar phase transition behaviour to achiral 3BC, and ferroelectric polarization-electric field (P-E) hysteresis curves were observed in the discotic hexagonal columnar (Colh) liquid crystal phase. Interestingly, the magnitudes of Pr and Et values of S-3BC were 5.5-times larger and 13-times smaller than those of 3BC because of the introduction of the chiral alkyl chains, indicating a useful method to obtain low voltage ON/OFF ratios for the switching device. Much stronger N-H⋯O hydrogen-bonding interactions were observed in S-3BC than in 3BC because of much shorter π-stacking distance and blue-shift of the intermolecular asymmetrical N-H vibrational band in the former, which effectively decreased the potential energy barrier for the dipole inversion between N-H⋯O and O⋯H-N orientations and the Et value.
AB - The phase transition behaviour, molecular assemblies, and dielectric responses of an N,N′,N′′-trialkylbenzene-1,3,5-tricarboxamide derivative bearing chiral (S)-3,7-dimethyloctyl chains (S-3BC) were compared with those of an N,N′,N′′-trioctadecylbenzene-1,3,5-tricarboxamide derivative (3BC) bearing achiral -CONHC14H29 chains. Chiral S-3BC showed a similar phase transition behaviour to achiral 3BC, and ferroelectric polarization-electric field (P-E) hysteresis curves were observed in the discotic hexagonal columnar (Colh) liquid crystal phase. Interestingly, the magnitudes of Pr and Et values of S-3BC were 5.5-times larger and 13-times smaller than those of 3BC because of the introduction of the chiral alkyl chains, indicating a useful method to obtain low voltage ON/OFF ratios for the switching device. Much stronger N-H⋯O hydrogen-bonding interactions were observed in S-3BC than in 3BC because of much shorter π-stacking distance and blue-shift of the intermolecular asymmetrical N-H vibrational band in the former, which effectively decreased the potential energy barrier for the dipole inversion between N-H⋯O and O⋯H-N orientations and the Et value.
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U2 - 10.1039/d0tc02414g
DO - 10.1039/d0tc02414g
M3 - Article
AN - SCOPUS:85089307056
SN - 2050-7526
VL - 8
SP - 10283
EP - 10289
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 30
ER -