Temperature dependence of spherical electron transfer in a nanosized [Fe<sub>14</sub>] complex.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31796745.
- Also identified by DOI 10.1038/s41467-019-13279-y and PMC identifier 6890645.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The study of transition metal clusters exhibiting fast electron hopping or delocalization remains challenging, because intermetallic communications mediated through bridging ligands are normally weak. Herein, we report the synthesis of a nanosized complex, [Fe(Tp)(CN)<sub>3</sub>]<sub>8</sub>[Fe(H<sub>2</sub>O)(DMSO)]<sub>6</sub> (abbreviated as [Fe<sub>14</sub>], Tp<sup>-</sup>, hydrotris(pyrazolyl)borate; DMSO, dimethyl sulfoxide), which has a fluctuating valence due to two mobile d-electrons in its atomic layer shell. The rate of electron transfer of [Fe<sub>14</sub>] complex demonstrates the Arrhenius-type temperature dependence in the nanosized spheric surface, wherein high-spin centers are ferromagnetically coupled, producing an S = 14 ground state. The electron-hopping rate at room temperature is faster than the time scale of Mössbauer measurements (<~10<sup>-8</sup> s). Partial reduction of N-terminal high spin Fe<sup>III</sup> sites and electron mediation ability of CN ligands lead to the observation of both an extensive electron transfer and magnetic coupling properties in a precisely atomic layered shell structure of a nanosized [Fe<sub>14</sub>] complex.