Air and moisture stable covalently-bonded tin() coordination polymers
Four covalently-bonded tin( ii ) coordination polymers, (1)-(4) , were hydrothermally prepared in aqueous alkaline media by the reactions of SnSO 4 with 1,2,4,5-benzenetetracarboxylic acid (1) , 1,3,5-benzenetricarboxylic acid (2) , 4-hydroxypyridine-2,6-dicarboxylic acid (3) , and 1,3,5-cyclohexane...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2018, Vol.47 (24), p.813-822 |
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creator | de Lima, G. M Walton, R. I Clarkson, G. J Bitzer, R. S Ardisson, J. D |
description | Four covalently-bonded tin(
ii
) coordination polymers,
(1)-(4)
, were hydrothermally prepared in aqueous alkaline media by the reactions of SnSO
4
with 1,2,4,5-benzenetetracarboxylic acid
(1)
, 1,3,5-benzenetricarboxylic acid
(2)
, 4-hydroxypyridine-2,6-dicarboxylic acid
(3)
, and 1,3,5-cyclohexanetricarboxylic acid
(4)
. All products were structurally authenticated by single-crystal X-ray diffraction, and the number of different tin centres and their oxidation states were confirmed by
119
Sn Mössbauer spectroscopy. In addition, the comparison between experimental and simulated X-ray powder diffraction patterns confirmed the authenticity of the samples. Our crystallographic results for
(1)-(4)
show that the Sn(
ii
) centres are tetracoordinated and exhibit distorted disphenoidal geometries, corroborating the presence of one stereochemically active lone electron pair at each metal site. Products
(1)
and
(2)
display bi-dimensional polymeric structures,
(3)
exhibits a one-dimensional architecture, whereas
(4)
shows a remarkable three-dimensional coordination network. Hirshfeld surface and supramolecular analyses for the repeating units of
(1)-(4)
were also performed in order to identify structurally important non-covalent interactions.
Compounds
(1)-(4)
display 1D, 2D or 3D coordination networks, in which the Sn(
ii
) cations exhibit distorted disphenoidal geometries due to the stereochemically active electron lone pairs. |
doi_str_mv | 10.1039/c8dt01370e |
format | Article |
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ii
) coordination polymers,
(1)-(4)
, were hydrothermally prepared in aqueous alkaline media by the reactions of SnSO
4
with 1,2,4,5-benzenetetracarboxylic acid
(1)
, 1,3,5-benzenetricarboxylic acid
(2)
, 4-hydroxypyridine-2,6-dicarboxylic acid
(3)
, and 1,3,5-cyclohexanetricarboxylic acid
(4)
. All products were structurally authenticated by single-crystal X-ray diffraction, and the number of different tin centres and their oxidation states were confirmed by
119
Sn Mössbauer spectroscopy. In addition, the comparison between experimental and simulated X-ray powder diffraction patterns confirmed the authenticity of the samples. Our crystallographic results for
(1)-(4)
show that the Sn(
ii
) centres are tetracoordinated and exhibit distorted disphenoidal geometries, corroborating the presence of one stereochemically active lone electron pair at each metal site. Products
(1)
and
(2)
display bi-dimensional polymeric structures,
(3)
exhibits a one-dimensional architecture, whereas
(4)
shows a remarkable three-dimensional coordination network. Hirshfeld surface and supramolecular analyses for the repeating units of
(1)-(4)
were also performed in order to identify structurally important non-covalent interactions.
Compounds
(1)-(4)
display 1D, 2D or 3D coordination networks, in which the Sn(
ii
) cations exhibit distorted disphenoidal geometries due to the stereochemically active electron lone pairs.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c8dt01370e</identifier><identifier>PMID: 29869660</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Acids ; Coordination polymers ; Covalence ; Crystal structure ; Crystallography ; Diffraction ; Diffraction patterns ; Mossbauer spectroscopy ; Oxidation ; Polymers ; Single crystals ; Tin ; X ray powder diffraction ; X-ray diffraction</subject><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2018, Vol.47 (24), p.813-822</ispartof><rights>Copyright Royal Society of Chemistry 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-3147750486cef0271eb0a46353812688b23e6d019b6b0e171cf3e5ff66abef693</citedby><cites>FETCH-LOGICAL-c403t-3147750486cef0271eb0a46353812688b23e6d019b6b0e171cf3e5ff66abef693</cites><orcidid>0000-0002-6940-3110 ; 0000-0001-9706-2774 ; 0000-0002-3816-0320</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29869660$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Lima, G. M</creatorcontrib><creatorcontrib>Walton, R. I</creatorcontrib><creatorcontrib>Clarkson, G. J</creatorcontrib><creatorcontrib>Bitzer, R. S</creatorcontrib><creatorcontrib>Ardisson, J. D</creatorcontrib><title>Air and moisture stable covalently-bonded tin() coordination polymers</title><title>Dalton transactions : an international journal of inorganic chemistry</title><addtitle>Dalton Trans</addtitle><description>Four covalently-bonded tin(
ii
) coordination polymers,
(1)-(4)
, were hydrothermally prepared in aqueous alkaline media by the reactions of SnSO
4
with 1,2,4,5-benzenetetracarboxylic acid
(1)
, 1,3,5-benzenetricarboxylic acid
(2)
, 4-hydroxypyridine-2,6-dicarboxylic acid
(3)
, and 1,3,5-cyclohexanetricarboxylic acid
(4)
. All products were structurally authenticated by single-crystal X-ray diffraction, and the number of different tin centres and their oxidation states were confirmed by
119
Sn Mössbauer spectroscopy. In addition, the comparison between experimental and simulated X-ray powder diffraction patterns confirmed the authenticity of the samples. Our crystallographic results for
(1)-(4)
show that the Sn(
ii
) centres are tetracoordinated and exhibit distorted disphenoidal geometries, corroborating the presence of one stereochemically active lone electron pair at each metal site. Products
(1)
and
(2)
display bi-dimensional polymeric structures,
(3)
exhibits a one-dimensional architecture, whereas
(4)
shows a remarkable three-dimensional coordination network. Hirshfeld surface and supramolecular analyses for the repeating units of
(1)-(4)
were also performed in order to identify structurally important non-covalent interactions.
Compounds
(1)-(4)
display 1D, 2D or 3D coordination networks, in which the Sn(
ii
) cations exhibit distorted disphenoidal geometries due to the stereochemically active electron lone pairs.</description><subject>Acids</subject><subject>Coordination polymers</subject><subject>Covalence</subject><subject>Crystal structure</subject><subject>Crystallography</subject><subject>Diffraction</subject><subject>Diffraction patterns</subject><subject>Mossbauer spectroscopy</subject><subject>Oxidation</subject><subject>Polymers</subject><subject>Single crystals</subject><subject>Tin</subject><subject>X ray powder diffraction</subject><subject>X-ray diffraction</subject><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpd0c1LwzAYBvAgipvTi3el4GUK1Xy0aXocc37AwMs8lyR9Cx1tMpN0sP_e1s0JnhKSHw9vniB0TfAjwSx_0qIMmLAMwwkakyTL4pyy5PS4p3yELrxfY0wpTuk5GtFc8JxzPEaLWe0iacqotbUPnYPIB6kaiLTdygZMaHaxsqaEMgq1md7359aVtZGhtiba2GbXgvOX6KySjYerwzpBny-L1fwtXn68vs9ny1gnmIWYDQOlOBFcQ4VpRkBhmXCWMkEoF0JRBrzEJFdcYSAZ0RWDtKo4lwoqnrMJmu5zN85-deBD0dZeQ9NIA7bzRf-8IZ3ztKd3_-jads700w2KZ4zkmejVw15pZ713UBUbV7fS7QqCi6HcYi6eVz_lLnp8e4jsVAvlkf622YObPXBeH2__fod9A7jFfLc</recordid><startdate>2018</startdate><enddate>2018</enddate><creator>de Lima, G. M</creator><creator>Walton, R. I</creator><creator>Clarkson, G. J</creator><creator>Bitzer, R. S</creator><creator>Ardisson, J. D</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6940-3110</orcidid><orcidid>https://orcid.org/0000-0001-9706-2774</orcidid><orcidid>https://orcid.org/0000-0002-3816-0320</orcidid></search><sort><creationdate>2018</creationdate><title>Air and moisture stable covalently-bonded tin() coordination polymers</title><author>de Lima, G. M ; Walton, R. I ; Clarkson, G. J ; Bitzer, R. S ; Ardisson, J. D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-3147750486cef0271eb0a46353812688b23e6d019b6b0e171cf3e5ff66abef693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Acids</topic><topic>Coordination polymers</topic><topic>Covalence</topic><topic>Crystal structure</topic><topic>Crystallography</topic><topic>Diffraction</topic><topic>Diffraction patterns</topic><topic>Mossbauer spectroscopy</topic><topic>Oxidation</topic><topic>Polymers</topic><topic>Single crystals</topic><topic>Tin</topic><topic>X ray powder diffraction</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Lima, G. M</creatorcontrib><creatorcontrib>Walton, R. I</creatorcontrib><creatorcontrib>Clarkson, G. J</creatorcontrib><creatorcontrib>Bitzer, R. S</creatorcontrib><creatorcontrib>Ardisson, J. D</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Lima, G. M</au><au>Walton, R. I</au><au>Clarkson, G. J</au><au>Bitzer, R. S</au><au>Ardisson, J. D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Air and moisture stable covalently-bonded tin() coordination polymers</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><addtitle>Dalton Trans</addtitle><date>2018</date><risdate>2018</risdate><volume>47</volume><issue>24</issue><spage>813</spage><epage>822</epage><pages>813-822</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>Four covalently-bonded tin(
ii
) coordination polymers,
(1)-(4)
, were hydrothermally prepared in aqueous alkaline media by the reactions of SnSO
4
with 1,2,4,5-benzenetetracarboxylic acid
(1)
, 1,3,5-benzenetricarboxylic acid
(2)
, 4-hydroxypyridine-2,6-dicarboxylic acid
(3)
, and 1,3,5-cyclohexanetricarboxylic acid
(4)
. All products were structurally authenticated by single-crystal X-ray diffraction, and the number of different tin centres and their oxidation states were confirmed by
119
Sn Mössbauer spectroscopy. In addition, the comparison between experimental and simulated X-ray powder diffraction patterns confirmed the authenticity of the samples. Our crystallographic results for
(1)-(4)
show that the Sn(
ii
) centres are tetracoordinated and exhibit distorted disphenoidal geometries, corroborating the presence of one stereochemically active lone electron pair at each metal site. Products
(1)
and
(2)
display bi-dimensional polymeric structures,
(3)
exhibits a one-dimensional architecture, whereas
(4)
shows a remarkable three-dimensional coordination network. Hirshfeld surface and supramolecular analyses for the repeating units of
(1)-(4)
were also performed in order to identify structurally important non-covalent interactions.
Compounds
(1)-(4)
display 1D, 2D or 3D coordination networks, in which the Sn(
ii
) cations exhibit distorted disphenoidal geometries due to the stereochemically active electron lone pairs.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>29869660</pmid><doi>10.1039/c8dt01370e</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-6940-3110</orcidid><orcidid>https://orcid.org/0000-0001-9706-2774</orcidid><orcidid>https://orcid.org/0000-0002-3816-0320</orcidid></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Acids Coordination polymers Covalence Crystal structure Crystallography Diffraction Diffraction patterns Mossbauer spectroscopy Oxidation Polymers Single crystals Tin X ray powder diffraction X-ray diffraction |
title | Air and moisture stable covalently-bonded tin() coordination polymers |
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