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{[Hg(SCN)3]2(μ-L)}2–: An Efficient Secondary Building Unit for the Synthesis of 2D Iron(II) Spin-Crossover Coordination Polymers
We report an unprecedented series of two-dimensional (2D) spin-crossover (SCO) heterobimetallic coordination polymers generically formulated as {FeII[(HgII(SCN)3)2](L) x }·Solv, where x = 2 for L = tvp (trans-(4,4′-vinylenedipyridine)) (1tvp), bpmh ((1E,2E)-1,2-bis(pyridin-4-ylmethylene)hydrazine...
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Published in: | Inorganic chemistry 2018-02, Vol.57 (3), p.1562-1571 |
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container_title | Inorganic chemistry |
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creator | Zhang, Daopeng Valverde-Muñoz, Francisco Javier Bartual-Murgui, Carlos Piñeiro-López, Lucía Muñoz, M. Carmen Real, José Antonio |
description | We report an unprecedented series of two-dimensional (2D) spin-crossover (SCO) heterobimetallic coordination polymers generically formulated as {FeII[(HgII(SCN)3)2](L) x }·Solv, where x = 2 for L = tvp (trans-(4,4′-vinylenedipyridine)) (1tvp), bpmh ((1E,2E)-1,2-bis(pyridin-4-ylmethylene)hydrazine) (1bpmh·nCH 3 OH; n = 0, 1), bpeh ((1E,2E)-1,2-bis(1-(pyridin-4-yl)ethylidene)hydrazine) (1bpeh·nH 2 O; n = 0, 1) and x = 2.33 for L = bpbz (1,4-bis(pyridin-4-yl)benzene) (1bpbz·nH 2 O; n = 0, 2/3). The results confirm that self-assembly of FeII, [HgII(SCN)4]2–, and ditopic rodlike bridging ligands L containing 4-pyridyl moieties favors the formation of linear [Fe(μ-L)] n 2n+ chains and in situ generated binuclear units {[HgII(SCN)3]2(μ-L)}2–. The latter act as bridges between adjacent chains generating robust 2D layers. The [FeIIN6] centers are equatorially surrounded by four NCS– groups and two axial N atoms of the organic ligand L. The compound 1tvp and the unsolvated form of 1bpmh undergo complete SCO centered at T 1/2 = 177 and 226 K, characterized by the enthalpy and entropy variations ΔH = 12.3 and 10.5 kJ mol–1 and ΔS = 69.4 and 48 J K–1 mol–1, respectively. The almost complete SCO of the unsolvated form of 1bpeh occurs at ca. T 1/2 = 119 K and exhibits a complete LIESST effect. Regardless of the degree of solvation, a half-spin conversion at T 1/2 < 100 K occurs for 1bpbz·nH 2 O, which becomes almost complete at p = 0.65 GPa. The labile solvent molecules present in 1bpmh·CH 3 OH and 1bpeh·H 2 O have a dramatic influence on the corresponding SCO behavior. |
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Carmen ; Real, José Antonio</creator><creatorcontrib>Zhang, Daopeng ; Valverde-Muñoz, Francisco Javier ; Bartual-Murgui, Carlos ; Piñeiro-López, Lucía ; Muñoz, M. Carmen ; Real, José Antonio</creatorcontrib><description>We report an unprecedented series of two-dimensional (2D) spin-crossover (SCO) heterobimetallic coordination polymers generically formulated as {FeII[(HgII(SCN)3)2](L) x }·Solv, where x = 2 for L = tvp (trans-(4,4′-vinylenedipyridine)) (1tvp), bpmh ((1E,2E)-1,2-bis(pyridin-4-ylmethylene)hydrazine) (1bpmh·nCH 3 OH; n = 0, 1), bpeh ((1E,2E)-1,2-bis(1-(pyridin-4-yl)ethylidene)hydrazine) (1bpeh·nH 2 O; n = 0, 1) and x = 2.33 for L = bpbz (1,4-bis(pyridin-4-yl)benzene) (1bpbz·nH 2 O; n = 0, 2/3). The results confirm that self-assembly of FeII, [HgII(SCN)4]2–, and ditopic rodlike bridging ligands L containing 4-pyridyl moieties favors the formation of linear [Fe(μ-L)] n 2n+ chains and in situ generated binuclear units {[HgII(SCN)3]2(μ-L)}2–. The latter act as bridges between adjacent chains generating robust 2D layers. The [FeIIN6] centers are equatorially surrounded by four NCS– groups and two axial N atoms of the organic ligand L. The compound 1tvp and the unsolvated form of 1bpmh undergo complete SCO centered at T 1/2 = 177 and 226 K, characterized by the enthalpy and entropy variations ΔH = 12.3 and 10.5 kJ mol–1 and ΔS = 69.4 and 48 J K–1 mol–1, respectively. The almost complete SCO of the unsolvated form of 1bpeh occurs at ca. T 1/2 = 119 K and exhibits a complete LIESST effect. Regardless of the degree of solvation, a half-spin conversion at T 1/2 < 100 K occurs for 1bpbz·nH 2 O, which becomes almost complete at p = 0.65 GPa. The labile solvent molecules present in 1bpmh·CH 3 OH and 1bpeh·H 2 O have a dramatic influence on the corresponding SCO behavior.</description><identifier>ISSN: 0020-1669</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/acs.inorgchem.7b02906</identifier><identifier>PMID: 29336572</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Inorganic chemistry, 2018-02, Vol.57 (3), p.1562-1571</ispartof><rights>Copyright © 2018 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a2622-92d6c495748878d68e9522810e364019af36d27f971ffdb7c2b35aa2400d54323</citedby><cites>FETCH-LOGICAL-a2622-92d6c495748878d68e9522810e364019af36d27f971ffdb7c2b35aa2400d54323</cites><orcidid>0000-0002-2302-561X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29336572$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Daopeng</creatorcontrib><creatorcontrib>Valverde-Muñoz, Francisco Javier</creatorcontrib><creatorcontrib>Bartual-Murgui, Carlos</creatorcontrib><creatorcontrib>Piñeiro-López, Lucía</creatorcontrib><creatorcontrib>Muñoz, M. Carmen</creatorcontrib><creatorcontrib>Real, José Antonio</creatorcontrib><title>{[Hg(SCN)3]2(μ-L)}2–: An Efficient Secondary Building Unit for the Synthesis of 2D Iron(II) Spin-Crossover Coordination Polymers</title><title>Inorganic chemistry</title><addtitle>Inorg. Chem</addtitle><description>We report an unprecedented series of two-dimensional (2D) spin-crossover (SCO) heterobimetallic coordination polymers generically formulated as {FeII[(HgII(SCN)3)2](L) x }·Solv, where x = 2 for L = tvp (trans-(4,4′-vinylenedipyridine)) (1tvp), bpmh ((1E,2E)-1,2-bis(pyridin-4-ylmethylene)hydrazine) (1bpmh·nCH 3 OH; n = 0, 1), bpeh ((1E,2E)-1,2-bis(1-(pyridin-4-yl)ethylidene)hydrazine) (1bpeh·nH 2 O; n = 0, 1) and x = 2.33 for L = bpbz (1,4-bis(pyridin-4-yl)benzene) (1bpbz·nH 2 O; n = 0, 2/3). The results confirm that self-assembly of FeII, [HgII(SCN)4]2–, and ditopic rodlike bridging ligands L containing 4-pyridyl moieties favors the formation of linear [Fe(μ-L)] n 2n+ chains and in situ generated binuclear units {[HgII(SCN)3]2(μ-L)}2–. The latter act as bridges between adjacent chains generating robust 2D layers. The [FeIIN6] centers are equatorially surrounded by four NCS– groups and two axial N atoms of the organic ligand L. The compound 1tvp and the unsolvated form of 1bpmh undergo complete SCO centered at T 1/2 = 177 and 226 K, characterized by the enthalpy and entropy variations ΔH = 12.3 and 10.5 kJ mol–1 and ΔS = 69.4 and 48 J K–1 mol–1, respectively. The almost complete SCO of the unsolvated form of 1bpeh occurs at ca. T 1/2 = 119 K and exhibits a complete LIESST effect. Regardless of the degree of solvation, a half-spin conversion at T 1/2 < 100 K occurs for 1bpbz·nH 2 O, which becomes almost complete at p = 0.65 GPa. The labile solvent molecules present in 1bpmh·CH 3 OH and 1bpeh·H 2 O have a dramatic influence on the corresponding SCO behavior.</description><issn>0020-1669</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkNFq2zAUhkXZaLNuj7Chy-TCmXRky9buWrddA2EdZIVBKUaxpVTFllLJHoQyGOwR9jp7hj3EnmQKSXu7q3Mu_v8_5_8QekvJlBKg72UdpsY6v6rvVDfNlwQE4QdoRDMgSUbJ1xdoREjcKefiCL0K4Z4QIljKD9ERCMZ4lsMI_Xy8uVyNF-WnCbuF8Z_fyXzyHf7--PUBn1h8rrWpjbI9Xqja2Ub6DT4dTNsYu8LX1vRYO4_7O4UXGxtHMAE7jeEMz7yz49lsghdrY5PSuxDcN-Vx6ZyPbtkbZ_Fn12465cNr9FLLNqg3-3mMri_Ov5SXyfzq46w8mScSOEAioOF1KrI8LYq8aHihRAZQUKIYTwkVUjPeQK5FTrVulnkNS5ZJCSkhTZYyYMdovMtde_cwqNBXnQm1altplRtCRUUR0zlN8yjNdtJ6-7pXulp708X-FSXVln8V-VfP_Ks9_-h7tz8xLDvVPLuegEcB3Qm2_ns3eBsb_yf0H8v7lVE</recordid><startdate>20180205</startdate><enddate>20180205</enddate><creator>Zhang, Daopeng</creator><creator>Valverde-Muñoz, Francisco Javier</creator><creator>Bartual-Murgui, Carlos</creator><creator>Piñeiro-López, Lucía</creator><creator>Muñoz, M. Carmen</creator><creator>Real, José Antonio</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2302-561X</orcidid></search><sort><creationdate>20180205</creationdate><title>{[Hg(SCN)3]2(μ-L)}2–: An Efficient Secondary Building Unit for the Synthesis of 2D Iron(II) Spin-Crossover Coordination Polymers</title><author>Zhang, Daopeng ; Valverde-Muñoz, Francisco Javier ; Bartual-Murgui, Carlos ; Piñeiro-López, Lucía ; Muñoz, M. Carmen ; Real, José Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a2622-92d6c495748878d68e9522810e364019af36d27f971ffdb7c2b35aa2400d54323</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Daopeng</creatorcontrib><creatorcontrib>Valverde-Muñoz, Francisco Javier</creatorcontrib><creatorcontrib>Bartual-Murgui, Carlos</creatorcontrib><creatorcontrib>Piñeiro-López, Lucía</creatorcontrib><creatorcontrib>Muñoz, M. Carmen</creatorcontrib><creatorcontrib>Real, José Antonio</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Inorganic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Daopeng</au><au>Valverde-Muñoz, Francisco Javier</au><au>Bartual-Murgui, Carlos</au><au>Piñeiro-López, Lucía</au><au>Muñoz, M. Carmen</au><au>Real, José Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>{[Hg(SCN)3]2(μ-L)}2–: An Efficient Secondary Building Unit for the Synthesis of 2D Iron(II) Spin-Crossover Coordination Polymers</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2018-02-05</date><risdate>2018</risdate><volume>57</volume><issue>3</issue><spage>1562</spage><epage>1571</epage><pages>1562-1571</pages><issn>0020-1669</issn><eissn>1520-510X</eissn><abstract>We report an unprecedented series of two-dimensional (2D) spin-crossover (SCO) heterobimetallic coordination polymers generically formulated as {FeII[(HgII(SCN)3)2](L) x }·Solv, where x = 2 for L = tvp (trans-(4,4′-vinylenedipyridine)) (1tvp), bpmh ((1E,2E)-1,2-bis(pyridin-4-ylmethylene)hydrazine) (1bpmh·nCH 3 OH; n = 0, 1), bpeh ((1E,2E)-1,2-bis(1-(pyridin-4-yl)ethylidene)hydrazine) (1bpeh·nH 2 O; n = 0, 1) and x = 2.33 for L = bpbz (1,4-bis(pyridin-4-yl)benzene) (1bpbz·nH 2 O; n = 0, 2/3). The results confirm that self-assembly of FeII, [HgII(SCN)4]2–, and ditopic rodlike bridging ligands L containing 4-pyridyl moieties favors the formation of linear [Fe(μ-L)] n 2n+ chains and in situ generated binuclear units {[HgII(SCN)3]2(μ-L)}2–. The latter act as bridges between adjacent chains generating robust 2D layers. The [FeIIN6] centers are equatorially surrounded by four NCS– groups and two axial N atoms of the organic ligand L. The compound 1tvp and the unsolvated form of 1bpmh undergo complete SCO centered at T 1/2 = 177 and 226 K, characterized by the enthalpy and entropy variations ΔH = 12.3 and 10.5 kJ mol–1 and ΔS = 69.4 and 48 J K–1 mol–1, respectively. The almost complete SCO of the unsolvated form of 1bpeh occurs at ca. T 1/2 = 119 K and exhibits a complete LIESST effect. Regardless of the degree of solvation, a half-spin conversion at T 1/2 < 100 K occurs for 1bpbz·nH 2 O, which becomes almost complete at p = 0.65 GPa. The labile solvent molecules present in 1bpmh·CH 3 OH and 1bpeh·H 2 O have a dramatic influence on the corresponding SCO behavior.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>29336572</pmid><doi>10.1021/acs.inorgchem.7b02906</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-2302-561X</orcidid></addata></record> |
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title | {[Hg(SCN)3]2(μ-L)}2–: An Efficient Secondary Building Unit for the Synthesis of 2D Iron(II) Spin-Crossover Coordination Polymers |
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