Higher-Temperature Dielectric Molecular Motor Induced by Unusual Chair-to-Rotator Motion.

Inorg Chem

Ordered Matter Science Research Center, Jiangsu Key Laboratory for Science and Applications of Molecular Ferroelectrics , Southeast University, Nanjing 211189 , P. R. China.

Published: April 2019

With regard to the artificial molecular motor that was recognized with the 2016 Nobel Prize, this success proves the great scientific significance of rotary motor-type motion at the molecular level, which has been expected to play an invaluable role in the development of electronic information molecular materials. However, designing electronic information-critical high-temperature molecular motors has always been a huge challenge. Since we discovered [(CH)NCHCl]MnCl, this cation rotation pattern with a motor-type motion structure has continued to attract our attention. Considering a strategy that combines molecular machines with dielectric theory, ( N, N-dimethylpiperidinium)CdCl, the new dielectric molecular motor material that exhibits superior physical properties, could be considered to be an excellent dielectric switch based on its electric field and temperature. Crystal structure analyses reveal that the reversible phase transition is mainly induced by the unusual chair-to-rotator motion of cations. Because of the unprecedented leaping structural transition from P6/ mmc to P2/ c and the rotating motor-type motion structure, the material exhibits remarkable anisotropy and outstanding dielectric switching characteristics. These findings open a new avenue for the design and assembly of novel molecular motor materials in the field of electronic information.

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.inorgchem.9b00161DOI Listing

Publication Analysis

Top Keywords

molecular motor
16
motor-type motion
12
molecular
8
dielectric molecular
8
induced unusual
8
unusual chair-to-rotator
8
chair-to-rotator motion
8
motion structure
8
material exhibits
8
motion
5

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!