Poly[(μ4-2,5-dimethoxybenzene-1,4-dicarboxylato)manganese(II)] and its zinc(II) analogue: three-dimensional coordination polymers containing unusually coordinated metal centres
The title compounds, [Mn(C10H8O6)]n and [Zn(C10H8O6)]n, are isomorphous coordination polymers prepared from 2,5‐dimethoxyterephthalic acid (H2dmt) and the respective metal(II) salts. Both complexes form three‐dimensional metal–organic frameworks with each MII centre bridged by four 2,5‐dimethoxytere...
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description | The title compounds, [Mn(C10H8O6)]n and [Zn(C10H8O6)]n, are isomorphous coordination polymers prepared from 2,5‐dimethoxyterephthalic acid (H2dmt) and the respective metal(II) salts. Both complexes form three‐dimensional metal–organic frameworks with each MII centre bridged by four 2,5‐dimethoxyterephthalate (dmt2−) anions, resulting in the same type of network topology. The asymmetric unit consists of one MII cation on a twofold axis and one half of a dmt2− anion (located on a centre of inversion). In the crystal structure, the MII centres are coordinated in a rather unusual way, as there is a distorted tetrahedral inner coordination sphere formed by four carboxylate O atoms of four different dmt2− anions, and an additional outer coordination sphere formed by two methoxy and two carboxylate O atoms, with each of the O atoms belonging to one of the four different dmt2− anions forming the inner coordination sphere. Consideration of both coordination spheres results in a super‐dodecahedral coordination geometry for the MII centres. Besides the numerous MII...O interactions, both structures are further stabilized by weak C—H...O contacts. |
doi_str_mv | 10.1107/S0108270110046950 |
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R. L.</creator><creatorcontrib>Böhle, Tony ; Eissmann, Frank ; Weber, Edwin ; Mertens, Florian O. R. L.</creatorcontrib><description>The title compounds, [Mn(C10H8O6)]n and [Zn(C10H8O6)]n, are isomorphous coordination polymers prepared from 2,5‐dimethoxyterephthalic acid (H2dmt) and the respective metal(II) salts. Both complexes form three‐dimensional metal–organic frameworks with each MII centre bridged by four 2,5‐dimethoxyterephthalate (dmt2−) anions, resulting in the same type of network topology. The asymmetric unit consists of one MII cation on a twofold axis and one half of a dmt2− anion (located on a centre of inversion). In the crystal structure, the MII centres are coordinated in a rather unusual way, as there is a distorted tetrahedral inner coordination sphere formed by four carboxylate O atoms of four different dmt2− anions, and an additional outer coordination sphere formed by two methoxy and two carboxylate O atoms, with each of the O atoms belonging to one of the four different dmt2− anions forming the inner coordination sphere. Consideration of both coordination spheres results in a super‐dodecahedral coordination geometry for the MII centres. 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R. L.</creatorcontrib><title>Poly[(μ4-2,5-dimethoxybenzene-1,4-dicarboxylato)manganese(II)] and its zinc(II) analogue: three-dimensional coordination polymers containing unusually coordinated metal centres</title><title>Acta crystallographica. Section C, Crystal structure communications</title><addtitle>Acta Cryst. C</addtitle><description>The title compounds, [Mn(C10H8O6)]n and [Zn(C10H8O6)]n, are isomorphous coordination polymers prepared from 2,5‐dimethoxyterephthalic acid (H2dmt) and the respective metal(II) salts. Both complexes form three‐dimensional metal–organic frameworks with each MII centre bridged by four 2,5‐dimethoxyterephthalate (dmt2−) anions, resulting in the same type of network topology. The asymmetric unit consists of one MII cation on a twofold axis and one half of a dmt2− anion (located on a centre of inversion). In the crystal structure, the MII centres are coordinated in a rather unusual way, as there is a distorted tetrahedral inner coordination sphere formed by four carboxylate O atoms of four different dmt2− anions, and an additional outer coordination sphere formed by two methoxy and two carboxylate O atoms, with each of the O atoms belonging to one of the four different dmt2− anions forming the inner coordination sphere. Consideration of both coordination spheres results in a super‐dodecahedral coordination geometry for the MII centres. Besides the numerous MII...O interactions, both structures are further stabilized by weak C—H...O contacts.</description><subject>Analogue</subject><subject>Coordination polymers</subject><subject>Crystal structure</subject><subject>Crystallography</subject><issn>0108-2701</issn><issn>1600-5759</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqFUcFu1DAQtRCILgsfwAXlRis1YMdx7HArK0hXqgAJEEIIWY49uzUk9mInoulfcecb-CYctpQDh56sefPeG888hB4S_IQQzJ--xQSLguNU4LKqGb6FFqTCOGec1bfRYm7nc_8A3YvxC8a4KAp6Fx0UpMAV5nSBfrzx3fTp8NfPMi-OWW5sD8O5v5hacJfgICfHZQK1Cm0COzX4o165rXIQ4XC9PvqcKWcyO8Ts0jo9IwlQnd-O8CwbzgPAH0sXrU9wpr0Pxjo1pDLbpck9hJhQNyjrrNtmoxvjqLpu-kcFk6U_zWJwQ4B4H93ZqC7Cg6t3id6_fPFudZqfvW7Wq5OzXJekZjmhaVdRM6E118LUbWGAbERNDDNVS1pmjN4wqErNqWqhpILidEJiKK1NS2u6RI_3vrvgv40QB9nbqKHr0vJ-jFIwxnE6tLiZWaQMRJnuvURkz9TBxxhgI3fB9ipMkmA5Ryr_izRpHl25j20P5lrxN8NEEHvCd9vBdLOjPPm4ahpalCxJ873UxgEurqUqfJUVp5zJD68aSavnp03Da4npb_xtvc0</recordid><startdate>201101</startdate><enddate>201101</enddate><creator>Böhle, Tony</creator><creator>Eissmann, Frank</creator><creator>Weber, Edwin</creator><creator>Mertens, Florian O. 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L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4195-132228958cc7c8d9b2de1f891d5d6b1b5ddcf5e64c73abe438306951d339db393</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Analogue</topic><topic>Coordination polymers</topic><topic>Crystal structure</topic><topic>Crystallography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Böhle, Tony</creatorcontrib><creatorcontrib>Eissmann, Frank</creatorcontrib><creatorcontrib>Weber, Edwin</creatorcontrib><creatorcontrib>Mertens, Florian O. R. 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L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Poly[(μ4-2,5-dimethoxybenzene-1,4-dicarboxylato)manganese(II)] and its zinc(II) analogue: three-dimensional coordination polymers containing unusually coordinated metal centres</atitle><jtitle>Acta crystallographica. Section C, Crystal structure communications</jtitle><addtitle>Acta Cryst. C</addtitle><date>2011-01</date><risdate>2011</risdate><volume>67</volume><issue>1</issue><spage>m5</spage><epage>m8</epage><pages>m5-m8</pages><issn>0108-2701</issn><eissn>1600-5759</eissn><abstract>The title compounds, [Mn(C10H8O6)]n and [Zn(C10H8O6)]n, are isomorphous coordination polymers prepared from 2,5‐dimethoxyterephthalic acid (H2dmt) and the respective metal(II) salts. Both complexes form three‐dimensional metal–organic frameworks with each MII centre bridged by four 2,5‐dimethoxyterephthalate (dmt2−) anions, resulting in the same type of network topology. The asymmetric unit consists of one MII cation on a twofold axis and one half of a dmt2− anion (located on a centre of inversion). In the crystal structure, the MII centres are coordinated in a rather unusual way, as there is a distorted tetrahedral inner coordination sphere formed by four carboxylate O atoms of four different dmt2− anions, and an additional outer coordination sphere formed by two methoxy and two carboxylate O atoms, with each of the O atoms belonging to one of the four different dmt2− anions forming the inner coordination sphere. Consideration of both coordination spheres results in a super‐dodecahedral coordination geometry for the MII centres. Besides the numerous MII...O interactions, both structures are further stabilized by weak C—H...O contacts.</abstract><cop>5 Abbey Square, Chester, Cheshire CH1 2HU, England</cop><pub>International Union of Crystallography</pub><pmid>21206073</pmid><doi>10.1107/S0108270110046950</doi></addata></record> |
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subjects | Analogue Coordination polymers Crystal structure Crystallography |
title | Poly[(μ4-2,5-dimethoxybenzene-1,4-dicarboxylato)manganese(II)] and its zinc(II) analogue: three-dimensional coordination polymers containing unusually coordinated metal centres |
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