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Crystalline Germanium(I) and Tin(I) Centered Radical Anions

An isostructural series of heavy Group 14 E(I) radical anions (Ge, Sn, Pb), stabilized by a bulky xanthene‐based diamido ligand are reported. The radical anions were synthesised by the one‐electron reduction of their corresponding E(II) precursor complexes with sodium naphthalenide in THF, yielding...

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Autores principales: Lim, Li Feng, Judd, Martyna, Vasko, Petra, Gardiner, Michael G., Pantazis, Dimitrios A., Cox, Nicholas, Hicks, Jamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401049/
https://www.ncbi.nlm.nih.gov/pubmed/35266609
http://dx.doi.org/10.1002/anie.202201248
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author Lim, Li Feng
Judd, Martyna
Vasko, Petra
Gardiner, Michael G.
Pantazis, Dimitrios A.
Cox, Nicholas
Hicks, Jamie
author_facet Lim, Li Feng
Judd, Martyna
Vasko, Petra
Gardiner, Michael G.
Pantazis, Dimitrios A.
Cox, Nicholas
Hicks, Jamie
author_sort Lim, Li Feng
collection PubMed
description An isostructural series of heavy Group 14 E(I) radical anions (Ge, Sn, Pb), stabilized by a bulky xanthene‐based diamido ligand are reported. The radical anions were synthesised by the one‐electron reduction of their corresponding E(II) precursor complexes with sodium naphthalenide in THF, yielding the radical anions as charge‐separated sodium salts. The series of main group radicals have been comprehensively characterized by EPR spectroscopy, X‐ray crystallography and DFT analysis, which reveal that in all cases, the spin density of the unpaired electron almost exclusively resides in a p‐orbital of π symmetry located on the Group 14 center.
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spelling pubmed-94010492022-08-26 Crystalline Germanium(I) and Tin(I) Centered Radical Anions Lim, Li Feng Judd, Martyna Vasko, Petra Gardiner, Michael G. Pantazis, Dimitrios A. Cox, Nicholas Hicks, Jamie Angew Chem Int Ed Engl Communications An isostructural series of heavy Group 14 E(I) radical anions (Ge, Sn, Pb), stabilized by a bulky xanthene‐based diamido ligand are reported. The radical anions were synthesised by the one‐electron reduction of their corresponding E(II) precursor complexes with sodium naphthalenide in THF, yielding the radical anions as charge‐separated sodium salts. The series of main group radicals have been comprehensively characterized by EPR spectroscopy, X‐ray crystallography and DFT analysis, which reveal that in all cases, the spin density of the unpaired electron almost exclusively resides in a p‐orbital of π symmetry located on the Group 14 center. John Wiley and Sons Inc. 2022-03-23 2022-05-16 /pmc/articles/PMC9401049/ /pubmed/35266609 http://dx.doi.org/10.1002/anie.202201248 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Lim, Li Feng
Judd, Martyna
Vasko, Petra
Gardiner, Michael G.
Pantazis, Dimitrios A.
Cox, Nicholas
Hicks, Jamie
Crystalline Germanium(I) and Tin(I) Centered Radical Anions
title Crystalline Germanium(I) and Tin(I) Centered Radical Anions
title_full Crystalline Germanium(I) and Tin(I) Centered Radical Anions
title_fullStr Crystalline Germanium(I) and Tin(I) Centered Radical Anions
title_full_unstemmed Crystalline Germanium(I) and Tin(I) Centered Radical Anions
title_short Crystalline Germanium(I) and Tin(I) Centered Radical Anions
title_sort crystalline germanium(i) and tin(i) centered radical anions
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401049/
https://www.ncbi.nlm.nih.gov/pubmed/35266609
http://dx.doi.org/10.1002/anie.202201248
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