Solid State Chemistry of Ten-Fold Coordinate Thorium(IV) Complexes with Oxalates in the Presence of Ammonium and Hydrazinium Ions

Double and triple thorium oxalates have been synthesized by successive evaporation of a solution of thorium nitrate, ammonium, or hydrazinium oxalate and hydrogen peroxide. Compounds M6Ca2Th2(C2O4)9­·nH2O (M = NH4 +, N2H5 +) (1) were first accidentally obtained due to the unexpected presence of calc...

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Veröffentlicht in:Crystal growth & design 2018-08, Vol.18 (8), p.4593-4601
Hauptverfasser: Blanchard, Florent, Rivenet, Murielle, Vigier, Nicolas, Hablot, Isabelle, Grandjean, Stéphane, Abraham, Francis
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container_end_page 4601
container_issue 8
container_start_page 4593
container_title Crystal growth & design
container_volume 18
creator Blanchard, Florent
Rivenet, Murielle
Vigier, Nicolas
Hablot, Isabelle
Grandjean, Stéphane
Abraham, Francis
description Double and triple thorium oxalates have been synthesized by successive evaporation of a solution of thorium nitrate, ammonium, or hydrazinium oxalate and hydrogen peroxide. Compounds M6Ca2Th2(C2O4)9­·nH2O (M = NH4 +, N2H5 +) (1) were first accidentally obtained due to the unexpected presence of calcium as impurities in the thorium nitrate used. Further evaporation led to the M2Th2(C2O4)5­·nH2O (M = NH4 +, N2H5 +) (2) precipitation. After an additional evaporation of 2 weeks, compounds (2) transform into M4Th­(C2O4)4­·nH2O (M = NH4 +, N2H5 +) (3). In the three compounds, thorium is coordinated by five bidentate oxalate ions. In (1) Th­(C2O4)5 entities share an oxalate ion to form dimeric units further connected by Ca­(C2O4)5 (M = NH4 +) or Ca­(C2O4)5­(H2O) (M = N2H5 +) entities to build three-dimensional (3D) frameworks. Compounds (2) exhibit a 3D honeycomb thorium oxalate framework. Compounds (3) contain chains of oxalate-shared Th­(C2O4)5 entities, whereas, in solution, the compound (NH4)2Th2­(C2O4)5­·1.5H2O (2) reacts with oxalate ions and turns into compound (NH4)4Th­(C2O4)4­·4H2O (3); in the solid state the chains of the compound (3) condense to form the 3D framework of the compound (2) and release solid ammonium oxalate.
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Compounds M6Ca2Th2(C2O4)9­·nH2O (M = NH4 +, N2H5 +) (1) were first accidentally obtained due to the unexpected presence of calcium as impurities in the thorium nitrate used. Further evaporation led to the M2Th2(C2O4)5­·nH2O (M = NH4 +, N2H5 +) (2) precipitation. After an additional evaporation of 2 weeks, compounds (2) transform into M4Th­(C2O4)4­·nH2O (M = NH4 +, N2H5 +) (3). In the three compounds, thorium is coordinated by five bidentate oxalate ions. In (1) Th­(C2O4)5 entities share an oxalate ion to form dimeric units further connected by Ca­(C2O4)5 (M = NH4 +) or Ca­(C2O4)5­(H2O) (M = N2H5 +) entities to build three-dimensional (3D) frameworks. Compounds (2) exhibit a 3D honeycomb thorium oxalate framework. Compounds (3) contain chains of oxalate-shared Th­(C2O4)5 entities, whereas, in solution, the compound (NH4)2Th2­(C2O4)5­·1.5H2O (2) reacts with oxalate ions and turns into compound (NH4)4Th­(C2O4)4­·4H2O (3); in the solid state the chains of the compound (3) condense to form the 3D framework of the compound (2) and release solid ammonium oxalate.</description><identifier>ISSN: 1528-7483</identifier><identifier>EISSN: 1528-7505</identifier><identifier>DOI: 10.1021/acs.cgd.8b00565</identifier><language>eng</language><publisher>American Chemical Society</publisher><subject>Chemical Sciences ; Material chemistry</subject><ispartof>Crystal growth &amp; design, 2018-08, Vol.18 (8), p.4593-4601</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a311t-6fb9c8cab005a51bfb7d326aac36db7b4c274a510c2dc9d2ba55e3058757e1143</citedby><cites>FETCH-LOGICAL-a311t-6fb9c8cab005a51bfb7d326aac36db7b4c274a510c2dc9d2ba55e3058757e1143</cites><orcidid>0000-0002-1362-0976 ; 0000-0002-1591-2075 ; 0000-0002-1183-7629 ; 0000-0002-1565-4299</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.cgd.8b00565$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.cgd.8b00565$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://hal.univ-lille.fr/hal-03159378$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Blanchard, Florent</creatorcontrib><creatorcontrib>Rivenet, Murielle</creatorcontrib><creatorcontrib>Vigier, Nicolas</creatorcontrib><creatorcontrib>Hablot, Isabelle</creatorcontrib><creatorcontrib>Grandjean, Stéphane</creatorcontrib><creatorcontrib>Abraham, Francis</creatorcontrib><title>Solid State Chemistry of Ten-Fold Coordinate Thorium(IV) Complexes with Oxalates in the Presence of Ammonium and Hydrazinium Ions</title><title>Crystal growth &amp; design</title><addtitle>Cryst. Growth Des</addtitle><description>Double and triple thorium oxalates have been synthesized by successive evaporation of a solution of thorium nitrate, ammonium, or hydrazinium oxalate and hydrogen peroxide. Compounds M6Ca2Th2(C2O4)9­·nH2O (M = NH4 +, N2H5 +) (1) were first accidentally obtained due to the unexpected presence of calcium as impurities in the thorium nitrate used. Further evaporation led to the M2Th2(C2O4)5­·nH2O (M = NH4 +, N2H5 +) (2) precipitation. After an additional evaporation of 2 weeks, compounds (2) transform into M4Th­(C2O4)4­·nH2O (M = NH4 +, N2H5 +) (3). In the three compounds, thorium is coordinated by five bidentate oxalate ions. In (1) Th­(C2O4)5 entities share an oxalate ion to form dimeric units further connected by Ca­(C2O4)5 (M = NH4 +) or Ca­(C2O4)5­(H2O) (M = N2H5 +) entities to build three-dimensional (3D) frameworks. Compounds (2) exhibit a 3D honeycomb thorium oxalate framework. 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Growth Des</addtitle><date>2018-08-01</date><risdate>2018</risdate><volume>18</volume><issue>8</issue><spage>4593</spage><epage>4601</epage><pages>4593-4601</pages><issn>1528-7483</issn><eissn>1528-7505</eissn><abstract>Double and triple thorium oxalates have been synthesized by successive evaporation of a solution of thorium nitrate, ammonium, or hydrazinium oxalate and hydrogen peroxide. Compounds M6Ca2Th2(C2O4)9­·nH2O (M = NH4 +, N2H5 +) (1) were first accidentally obtained due to the unexpected presence of calcium as impurities in the thorium nitrate used. Further evaporation led to the M2Th2(C2O4)5­·nH2O (M = NH4 +, N2H5 +) (2) precipitation. After an additional evaporation of 2 weeks, compounds (2) transform into M4Th­(C2O4)4­·nH2O (M = NH4 +, N2H5 +) (3). In the three compounds, thorium is coordinated by five bidentate oxalate ions. In (1) Th­(C2O4)5 entities share an oxalate ion to form dimeric units further connected by Ca­(C2O4)5 (M = NH4 +) or Ca­(C2O4)5­(H2O) (M = N2H5 +) entities to build three-dimensional (3D) frameworks. Compounds (2) exhibit a 3D honeycomb thorium oxalate framework. Compounds (3) contain chains of oxalate-shared Th­(C2O4)5 entities, whereas, in solution, the compound (NH4)2Th2­(C2O4)5­·1.5H2O (2) reacts with oxalate ions and turns into compound (NH4)4Th­(C2O4)4­·4H2O (3); in the solid state the chains of the compound (3) condense to form the 3D framework of the compound (2) and release solid ammonium oxalate.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.cgd.8b00565</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-1362-0976</orcidid><orcidid>https://orcid.org/0000-0002-1591-2075</orcidid><orcidid>https://orcid.org/0000-0002-1183-7629</orcidid><orcidid>https://orcid.org/0000-0002-1565-4299</orcidid></addata></record>
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title Solid State Chemistry of Ten-Fold Coordinate Thorium(IV) Complexes with Oxalates in the Presence of Ammonium and Hydrazinium Ions
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