| Literature DB >> 32428358 |
Yoji Horii1, Marko Damjanović2,3, M R Ajayakumar4, Keiichi Katoh1, Yasutaka Kitagawa5, Liviu Chibotaru6, Liviu Ungur7, Marta Mas-Torrent4, Wolfgang Wernsdorfer3, Brian K Breedlove1, Markus Enders2, Jaume Veciana4, Masahiro Yamashita1,8,9.
Abstract
Presented here is a comprehensive study of highly oxidized multiple-decker complexes composed of TbIII and <span class="Chemical">CdII ions and two to five phthalocyaninato ligands, which are stabilized by electron-donating n-butoxy groups. From X-ray structural analyses, all the complexes become axially compressed upon ligand oxidation, resulting in bowl-shaped distortions of the ligands. In addition, unusual coexistence of square antiprism and square prism geometries around metal ions was observed in +4e charged species. From paramagnetic 1 H NMR studies on the resulting series of triple, quadruple and quintuple-decker complexes, ligand oxidation leads to a decrease in the magnetic anisotropy, as predicted from theoretical calculations. Unusual paramagnetic shifts were observed in the spectra of the +2e charged quadruple and quintuple-decker complexes, indicating that those two species are actually unexpected triplet biradicals. Magnetic measurements revealed that the series of complexes show single-molecule magnet properties, which are controlled by the multi-step redox induced structural changes.Entities:
Keywords: NMR; biradical; crystal engineering; magnetic anisotropy; redox
Year: 2020 PMID: 32428358 DOI: 10.1002/chem.202001365
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236