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Dicyanometallates as Model Extended Frameworks

[Image: see text] We report the structures of eight new dicyanometallate frameworks containing molecular extra-framework cations. These systems include a number of hybrid inorganic–organic analogues of conventional ceramics, such as Ruddlesden–Popper phases and perovskites. The structure types adopt...

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Autores principales: Hill, Joshua A., Thompson, Amber L., Goodwin, Andrew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2016
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894656/
https://www.ncbi.nlm.nih.gov/pubmed/27057759
http://dx.doi.org/10.1021/jacs.5b13446
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author Hill, Joshua A.
Thompson, Amber L.
Goodwin, Andrew L.
author_facet Hill, Joshua A.
Thompson, Amber L.
Goodwin, Andrew L.
author_sort Hill, Joshua A.
collection PubMed
description [Image: see text] We report the structures of eight new dicyanometallate frameworks containing molecular extra-framework cations. These systems include a number of hybrid inorganic–organic analogues of conventional ceramics, such as Ruddlesden–Popper phases and perovskites. The structure types adopted are rationalized in the broader context of all known dicyanometallate framework structures. We show that the structural diversity of this family can be understood in terms of (i) the charge and coordination preferences of the particular metal cation acting as framework node, and (ii) the size, shape, and extent of incorporation of extra-framework cations. In this way, we suggest that dicyanometallates form a particularly attractive model family of extended frameworks in which to explore the interplay between molecular degrees of freedom, framework topology, and supramolecular interactions.
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spelling pubmed-48946562016-06-07 Dicyanometallates as Model Extended Frameworks Hill, Joshua A. Thompson, Amber L. Goodwin, Andrew L. J Am Chem Soc [Image: see text] We report the structures of eight new dicyanometallate frameworks containing molecular extra-framework cations. These systems include a number of hybrid inorganic–organic analogues of conventional ceramics, such as Ruddlesden–Popper phases and perovskites. The structure types adopted are rationalized in the broader context of all known dicyanometallate framework structures. We show that the structural diversity of this family can be understood in terms of (i) the charge and coordination preferences of the particular metal cation acting as framework node, and (ii) the size, shape, and extent of incorporation of extra-framework cations. In this way, we suggest that dicyanometallates form a particularly attractive model family of extended frameworks in which to explore the interplay between molecular degrees of freedom, framework topology, and supramolecular interactions. American Chemical Society 2016-04-08 2016-05-11 /pmc/articles/PMC4894656/ /pubmed/27057759 http://dx.doi.org/10.1021/jacs.5b13446 Text en Copyright © 2016 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Hill, Joshua A.
Thompson, Amber L.
Goodwin, Andrew L.
Dicyanometallates as Model Extended Frameworks
title Dicyanometallates as Model Extended Frameworks
title_full Dicyanometallates as Model Extended Frameworks
title_fullStr Dicyanometallates as Model Extended Frameworks
title_full_unstemmed Dicyanometallates as Model Extended Frameworks
title_short Dicyanometallates as Model Extended Frameworks
title_sort dicyanometallates as model extended frameworks
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4894656/
https://www.ncbi.nlm.nih.gov/pubmed/27057759
http://dx.doi.org/10.1021/jacs.5b13446
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