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Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes

The three isomorphous [3.3.1] metallacryptate complexes bis­(pyridinium) di­aqua­dipyridine­hexa­kis­[μ(3)-salicyl­hydroximato(3−)]bis­[μ(2)-salicyl­hydroxim­ato(1−)]hexa­aluminiumgadolinium–pyridine–water (1/7.396/1), (C(5)H(6)N)(2)[GdAl(6)(C(7)H(6)NO(3))(2)(C(7)H(4)NO(3))(7)(C(5)H(5)N)(1.855)(H(2)...

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Autores principales: Rheam, Rachel E., Zeller, Matthias, Zaleski, Curtis M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472759/
https://www.ncbi.nlm.nih.gov/pubmed/32939300
http://dx.doi.org/10.1107/S2056989020010725
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author Rheam, Rachel E.
Zeller, Matthias
Zaleski, Curtis M.
author_facet Rheam, Rachel E.
Zeller, Matthias
Zaleski, Curtis M.
author_sort Rheam, Rachel E.
collection PubMed
description The three isomorphous [3.3.1] metallacryptate complexes bis­(pyridinium) di­aqua­dipyridine­hexa­kis­[μ(3)-salicyl­hydroximato(3−)]bis­[μ(2)-salicyl­hydroxim­ato(1−)]hexa­aluminiumgadolinium–pyridine–water (1/7.396/1), (C(5)H(6)N)(2)[GdAl(6)(C(7)H(6)NO(3))(2)(C(7)H(4)NO(3))(7)(C(5)H(5)N)(1.855)(H(2)O)(2)]·7.396C(5)H(5)N·H(2)O or [Hpy](2)[GdAl(6)(H(2)shi)(2)(shi)(7)(py)(1.855)(H(2)O)(2)]·7.396py·H(2)O, 1, bis­(pyridinium) di­aqua­dipyridine­hexa­kis­[μ(3)-salicyl­hydroximato(3−)]bis­[μ(2)-salicyl­hydroxim­ato(1−)]hexa­aluminiumdysprosium–pyridine–water (1/7.429/1), (C(5)H(6)N)(2)[DyAl(6)(C(7)H(6)NO(3))(2)(C(7)H(4)NO(3))(7)(C(5)H(5)N)(1.855)(H(2)O)(2)]·7.429C(5)H(5)N·H(2)O or [Hpy](2)[DyAl(6)(H(2)shi)(2)(shi)(7)(py)(1.891)(H(2)O)(2)]·7.429py·H(2)O, 2, and bis­(pyrid­in­ium) di­aqua­dipyridine­hexa­kis­[μ(3)-salicyl­hydroximato(3−)]bis­[μ(2)-salicyl­hydrox­imato(1−)]hexa­aluminiumytterbium–pyridine–water (1/7.386/1), (C(5)H(6)N)(2)[YbAl(6)(C(7)H(6)NO(3))(2)(C(7)H(4)NO(3))(7)(C(5)H(5)N)(1.855)(H(2)O)(2)]·7.429C(5)H(5)N·H(2)O or [Hpy](2)[YbAl(6)(H(2)shi)(2)(shi)(7)(py)(1.818)(H(2)O)(2)]·7.386py·H(2)O, 3, where Hpy(+) is pyridinium, shi(3−) is salicyl­hydroximate, and py is pyridine, consist of an aluminium-based metallacryptand that captures an Ln (III) ion in the central cavity. The metallacryptand portions are comprised of an Al—N—O repeat unit; thus, they can be considered three-dimensional metallacrowns. The encapsulated Ln (III) ions are nine-coordinate with a spherical capped-square-anti­prism geometry, while the six Al(III) ions are all octa­hedral. Four of the Al(III) ions are chiral centers with 2 Δ and 2 Λ stereoconfigurations. The remaining two Al(III) ions have trans chelate rings from two different shi(3−) ligands. For 1–3, a section of the main mol­ecule is disordered induced by the presence or absence of a pyridine ligand coordinated to one of the Al(III) ions. In the absence of the pyridine moiety, an H(2)shi(−) ligand moves into the space otherwise occupied by the pyridine and the phenol oxygen atom coordinates to the Al(III) ion. The movement of the H(2)shi(−) ligand induces movement for the Ln (III) ion, for another Al(III) ion that also binds the same H(2)shi(−) ligand, and for one of the shi(3−) ligands coordinated to the latter Al(III) ion. For 1–3 the occupancy ratio of the metallacryptand portions refined to 0.8550 (13):0.1450 (13), to 0.8909 (13):0.1091 (13), and to 0.8181 (14):0.1819 (14), respectively.
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spelling pubmed-74727592020-09-15 Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes Rheam, Rachel E. Zeller, Matthias Zaleski, Curtis M. Acta Crystallogr E Crystallogr Commun Research Communications The three isomorphous [3.3.1] metallacryptate complexes bis­(pyridinium) di­aqua­dipyridine­hexa­kis­[μ(3)-salicyl­hydroximato(3−)]bis­[μ(2)-salicyl­hydroxim­ato(1−)]hexa­aluminiumgadolinium–pyridine–water (1/7.396/1), (C(5)H(6)N)(2)[GdAl(6)(C(7)H(6)NO(3))(2)(C(7)H(4)NO(3))(7)(C(5)H(5)N)(1.855)(H(2)O)(2)]·7.396C(5)H(5)N·H(2)O or [Hpy](2)[GdAl(6)(H(2)shi)(2)(shi)(7)(py)(1.855)(H(2)O)(2)]·7.396py·H(2)O, 1, bis­(pyridinium) di­aqua­dipyridine­hexa­kis­[μ(3)-salicyl­hydroximato(3−)]bis­[μ(2)-salicyl­hydroxim­ato(1−)]hexa­aluminiumdysprosium–pyridine–water (1/7.429/1), (C(5)H(6)N)(2)[DyAl(6)(C(7)H(6)NO(3))(2)(C(7)H(4)NO(3))(7)(C(5)H(5)N)(1.855)(H(2)O)(2)]·7.429C(5)H(5)N·H(2)O or [Hpy](2)[DyAl(6)(H(2)shi)(2)(shi)(7)(py)(1.891)(H(2)O)(2)]·7.429py·H(2)O, 2, and bis­(pyrid­in­ium) di­aqua­dipyridine­hexa­kis­[μ(3)-salicyl­hydroximato(3−)]bis­[μ(2)-salicyl­hydrox­imato(1−)]hexa­aluminiumytterbium–pyridine–water (1/7.386/1), (C(5)H(6)N)(2)[YbAl(6)(C(7)H(6)NO(3))(2)(C(7)H(4)NO(3))(7)(C(5)H(5)N)(1.855)(H(2)O)(2)]·7.429C(5)H(5)N·H(2)O or [Hpy](2)[YbAl(6)(H(2)shi)(2)(shi)(7)(py)(1.818)(H(2)O)(2)]·7.386py·H(2)O, 3, where Hpy(+) is pyridinium, shi(3−) is salicyl­hydroximate, and py is pyridine, consist of an aluminium-based metallacryptand that captures an Ln (III) ion in the central cavity. The metallacryptand portions are comprised of an Al—N—O repeat unit; thus, they can be considered three-dimensional metallacrowns. The encapsulated Ln (III) ions are nine-coordinate with a spherical capped-square-anti­prism geometry, while the six Al(III) ions are all octa­hedral. Four of the Al(III) ions are chiral centers with 2 Δ and 2 Λ stereoconfigurations. The remaining two Al(III) ions have trans chelate rings from two different shi(3−) ligands. For 1–3, a section of the main mol­ecule is disordered induced by the presence or absence of a pyridine ligand coordinated to one of the Al(III) ions. In the absence of the pyridine moiety, an H(2)shi(−) ligand moves into the space otherwise occupied by the pyridine and the phenol oxygen atom coordinates to the Al(III) ion. The movement of the H(2)shi(−) ligand induces movement for the Ln (III) ion, for another Al(III) ion that also binds the same H(2)shi(−) ligand, and for one of the shi(3−) ligands coordinated to the latter Al(III) ion. For 1–3 the occupancy ratio of the metallacryptand portions refined to 0.8550 (13):0.1450 (13), to 0.8909 (13):0.1091 (13), and to 0.8181 (14):0.1819 (14), respectively. International Union of Crystallography 2020-08-14 /pmc/articles/PMC7472759/ /pubmed/32939300 http://dx.doi.org/10.1107/S2056989020010725 Text en © Rheam et al. 2020 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/
spellingShingle Research Communications
Rheam, Rachel E.
Zeller, Matthias
Zaleski, Curtis M.
Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes
title Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes
title_full Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes
title_fullStr Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes
title_full_unstemmed Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes
title_short Crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes
title_sort crystal structures of three anionic lanthanide–aluminium [3.3.1] metallacryptate complexes
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472759/
https://www.ncbi.nlm.nih.gov/pubmed/32939300
http://dx.doi.org/10.1107/S2056989020010725
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