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Large‐Amplitude Thermal Vibration‐Coupled Valence Tautomeric Transition Observed in a Conductive One‐Dimensional Rhodium–Dioxolene Complex
Author(s) -
Mitsumi Minoru,
Komatsu Yuuki,
Hashimoto Masahiro,
Toriumi Koshiro,
Kitagawa Yasutaka,
Miyazaki Yuji,
Akutsu Hiroki,
Akashi Haruo
Publication year - 2021
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.202004217
Subject(s) - rhodium , valence (chemistry) , tautomer , x ray photoelectron spectroscopy , amplitude , chemistry , chemical physics , phase transition , vibration , crystallography , molecular physics , materials science , computational chemistry , condensed matter physics , stereochemistry , nuclear magnetic resonance , physics , catalysis , organic chemistry , quantum mechanics
The exploration of dynamic molecular crystals is a fascinating theme for materials scientists owing to their fundamental science and potential application to molecular devices. Herein, a one‐dimensional (1D) rhodium‐dioxolene complex is reported that exhibits drastic changes in properties with the phase transition. X‐ray photoelectron spectroscopy (XPS) revealed that the room‐temperature (RT) phase is in a mixed‐valence state, and therefore, the drastic changes originate from the mixed‐valence state appearing in the RT phase. Another notable feature is that the mean square displacements of the rhodium atoms along the 1D chain dramatically increased in the RT phase, indicating a large‐amplitude vibration of the Rh−Rh bonds. From these results, a possible mechanism for the appearance of the mixed‐valence state in the RT phase was proposed based on the thermal electron transfer from the 1D d‐band to the semiquinonato π* orbital coupled with the large‐amplitude vibration of the Rh−Rh bonds.