Extended chains in vanadium O-centered complex V4OSe8I5∞: synthesis and structure
O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a pac...
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Veröffentlicht in: | Dalton transactions : an international journal of inorganic chemistry 2024-12 |
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creator | Galiev, R R Komarov, V Y Ryzhikov, M R Kozlova, S G Kuznetsov, V A Grayfer, E D Artemkina, S B Fedorov, V E |
description | O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations.O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations. |
doi_str_mv | 10.1039/d4dt02758b |
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Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations.O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations.</description><identifier>ISSN: 1477-9234</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/d4dt02758b</identifier><language>eng</language><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2024-12</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Galiev, R R</creatorcontrib><creatorcontrib>Komarov, V Y</creatorcontrib><creatorcontrib>Ryzhikov, M R</creatorcontrib><creatorcontrib>Kozlova, S G</creatorcontrib><creatorcontrib>Kuznetsov, V A</creatorcontrib><creatorcontrib>Grayfer, E D</creatorcontrib><creatorcontrib>Artemkina, S B</creatorcontrib><creatorcontrib>Fedorov, V E</creatorcontrib><title>Extended chains in vanadium O-centered complex V4OSe8I5∞: synthesis and structure</title><title>Dalton transactions : an international journal of inorganic chemistry</title><description>O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations.O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations.</description><issn>1477-9234</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqVjr0KwjAURoMo-Lv4BBldqmma2tZVFJ0cFNcSmytG2lR7E9E38Cl8OJ9EBQdXp-_AOcNHSN9nQ58FyUgJZRmPwnhXIy1fRJGX8EDUf7hJ2ohHxjhnIW-R9exqwShQNDtIbZBqQy_SSKVdQVdeBsZC9bFlccrhSrditYZ4GT7vjwnFm7EHQI1UGkXRVi6zroIuaexljtD7bocM5rPNdOGdqvLsAG1aaMwgz6WB0mEavM-JeCyScfBH-gJE0EpY</recordid><startdate>20241220</startdate><enddate>20241220</enddate><creator>Galiev, R R</creator><creator>Komarov, V Y</creator><creator>Ryzhikov, M R</creator><creator>Kozlova, S G</creator><creator>Kuznetsov, V A</creator><creator>Grayfer, E D</creator><creator>Artemkina, S B</creator><creator>Fedorov, V E</creator><scope>7X8</scope></search><sort><creationdate>20241220</creationdate><title>Extended chains in vanadium O-centered complex V4OSe8I5∞: synthesis and structure</title><author>Galiev, R R ; Komarov, V Y ; Ryzhikov, M R ; Kozlova, S G ; Kuznetsov, V A ; Grayfer, E D ; Artemkina, S B ; Fedorov, V E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_31474864963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Galiev, R R</creatorcontrib><creatorcontrib>Komarov, V Y</creatorcontrib><creatorcontrib>Ryzhikov, M R</creatorcontrib><creatorcontrib>Kozlova, S G</creatorcontrib><creatorcontrib>Kuznetsov, V A</creatorcontrib><creatorcontrib>Grayfer, E D</creatorcontrib><creatorcontrib>Artemkina, S B</creatorcontrib><creatorcontrib>Fedorov, V E</creatorcontrib><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>Galiev, R R</au><au>Komarov, V Y</au><au>Ryzhikov, M R</au><au>Kozlova, S G</au><au>Kuznetsov, V A</au><au>Grayfer, E D</au><au>Artemkina, S B</au><au>Fedorov, V E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extended chains in vanadium O-centered complex V4OSe8I5∞: synthesis and structure</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><date>2024-12-20</date><risdate>2024</risdate><issn>1477-9234</issn><eissn>1477-9234</eissn><abstract>O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations.O-centered tetranuclear vanadium selenoiodide [V4OSe8I5]∞ (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group C2/c, a = 21.146(2) Å, b = 5.8953(5) Å, c = 18.735(1) Å, β = 126.421(2)°, V = 1879.4(3) Å3, T = 150 K, Z = 4) is a packing of chains built from O-centered tetranuclear [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4] fragments. In the O-centered fragment, vanadium atoms form a distorted tetrahedron around an oxygen atom, V atoms are bridged by four μ2-(Se2)2- and two I- ligands. The latter iodide ligands bridge the neighboring fragments, thus forming a chain [V4(μ4-O)(μ-Se2)4(μ4-I)2/2I4]∞. The synthesis of the chain [V4OSe8I5]∞ takes place at the temperature of 290 °C, while at lower temperatures (220-250 °C) molecular compounds [V4OSe8I6]·X form. The direct 'cluster to chain' transformation is also observed and discussed in this work. Electrical resistance of the [V4OSe8I5]∞ polycrystalline pressed sample shows that the compound 1 is a narrow gap semiconductor, which is in agreement with the DFT calculations.</abstract><doi>10.1039/d4dt02758b</doi></addata></record> |
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title | Extended chains in vanadium O-centered complex V4OSe8I5∞: synthesis and structure |
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