Abstract
To test the coordination symmetry effect on the magnetization-reversal barrier trend of ErIII-based single-ion magnets, the C2v-symmetric organolanthanide anion [Er(Cp)2(OtBu)2]- has been incorporated with different countercations, resulting in two structures, namely, the discrete [K2(Cp)(18-C-6)2][Er(Cp)2(OtBu)2] (1) and the polymeric [ErK2(Cp)3(OtBu)2(THF)2]n (2), where 18-C-6 = 18-crown-6 ether and Cp = cyclopentadienide. Surprisingly, the polymeric 2 exhibits much stronger field-induced magnetization relaxing behavior compared to the monomeric 1. Such disparate dynamic magnetism is attributable to the subtle coordination environmental perturbations of the central ErIII ions.
Original language | English (US) |
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Pages (from-to) | 4588-4590 |
Number of pages | 3 |
Journal | Inorganic Chemistry |
Volume | 54 |
Issue number | 10 |
DOIs | |
State | Published - May 18 2015 |
Externally published | Yes |
ASJC Scopus subject areas
- Physical and Theoretical Chemistry
- Inorganic Chemistry
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CCDC 1036789: Experimental Crystal Structure Determination
Han, T. (Creator), Ding, Y. (Creator), Leng, J. (Creator), Zheng, Z. (Creator) & Zheng, Y. (Creator), Cambridge Crystallographic Data Centre, 2015
DOI: 10.5517/cc13svtk, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc13svtk&sid=DataCite
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CCDC 1036788: Experimental Crystal Structure Determination
Han, T. (Creator), Ding, Y. (Creator), Leng, J. (Creator), Zheng, Z. (Creator) & Zheng, Y. (Creator), Cambridge Crystallographic Data Centre, 2015
DOI: 10.5517/cc13svsj, http://www.ccdc.cam.ac.uk/services/structure_request?id=doi:10.5517/cc13svsj&sid=DataCite
Dataset