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Supramolecular assembly and structural transformation of d10-metal complexes containing (aza-15-crown-5)dithiocarbamate
The reaction of potassium (aza-15-crown-5)dithiocarbamate (KO4NCS2) and (Me2S)AuCl gave the dinuclear complex [Au(O4NCS2)]2, which underwent structural transformation upon heating to rearrange into the hexanuclear complex [Au(O4NCS2)]6. Under similar reaction conditions, KO4NCS2 reacted with AgNO3 o...
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Published in: | Dalton transactions : an international journal of inorganic chemistry 2022-11, Vol.51 (44), p.16973-16981 |
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creator | Tzeng, Biing-Chiau Chung-Lun, Wu Jun-Wei, Hung Su-Ying, Chien Gene-Hsiang, Lee |
description | The reaction of potassium (aza-15-crown-5)dithiocarbamate (KO4NCS2) and (Me2S)AuCl gave the dinuclear complex [Au(O4NCS2)]2, which underwent structural transformation upon heating to rearrange into the hexanuclear complex [Au(O4NCS2)]6. Under similar reaction conditions, KO4NCS2 reacted with AgNO3 or [Cu(CH3CN)4]ClO4 to give the 1-D coordination polymer [Ag(O4NCS2)]n (1) and the tetranuclear complex [Cu(O4NCS2)]4 (2), respectively. It is noted that upon heating a similar structural transformation process occurs from tetranuclear complex 2 to the octanuclear complex [Cu(O4NCS2)]8 (2′), connected by a weak Cu⋯S contact of 2.846 Å, and it has been isolated and corroborated by powder and single-crystal X-ray diffraction studies as well. Moreover, a variety of MO4NCS2 salts (M = Li+, Na+, K+ and Rb+) were used to react with AgNO3 to construct a series of coordination architectures: [LiAg(O4NCS2)2(μ-H2O)0.5]2 (3), {Na[Ag(O4NCS2)2]}n (4), {K[Ag(O4NCS2)2]}n (5) and {Rb[Ag(O4NCS2)2]}n (6). The smallest Li+ ion only coordinates with four oxygen atoms from the same azacrown ether ring and one H2O molecule, leading to a 1-D hydrogen-bonded chain with another azacrown ether ring for complex 3. The larger Na+ ion coordinates with seven oxygen atoms from two different crown ether rings, leading to a 1-D chain for complex 4. However, the largest K+ and Rb+ ions constitute a 1-D framework, except that each metal ion coordinates with eight oxygen atoms from two different crown ether rings, featuring a 1-D helical chain for complexes 5 and 6. Hence, the different sizes of alkaline metal ions exert a dramatic effect on the structural motifs of complexes 3–6. Remarkably, the dithiocarbamate moieties adopt μ2-bridging ([Au(O4NCS2)]2 and [Au(O4NCS2)]6), μ3- and μ4-bridging (1–2) and chelate forms (3–6) in the structural backbones. |
doi_str_mv | 10.1039/d2dt02768b |
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Under similar reaction conditions, KO4NCS2 reacted with AgNO3 or [Cu(CH3CN)4]ClO4 to give the 1-D coordination polymer [Ag(O4NCS2)]n (1) and the tetranuclear complex [Cu(O4NCS2)]4 (2), respectively. It is noted that upon heating a similar structural transformation process occurs from tetranuclear complex 2 to the octanuclear complex [Cu(O4NCS2)]8 (2′), connected by a weak Cu⋯S contact of 2.846 Å, and it has been isolated and corroborated by powder and single-crystal X-ray diffraction studies as well. Moreover, a variety of MO4NCS2 salts (M = Li+, Na+, K+ and Rb+) were used to react with AgNO3 to construct a series of coordination architectures: [LiAg(O4NCS2)2(μ-H2O)0.5]2 (3), {Na[Ag(O4NCS2)2]}n (4), {K[Ag(O4NCS2)2]}n (5) and {Rb[Ag(O4NCS2)2]}n (6). The smallest Li+ ion only coordinates with four oxygen atoms from the same azacrown ether ring and one H2O molecule, leading to a 1-D hydrogen-bonded chain with another azacrown ether ring for complex 3. The larger Na+ ion coordinates with seven oxygen atoms from two different crown ether rings, leading to a 1-D chain for complex 4. However, the largest K+ and Rb+ ions constitute a 1-D framework, except that each metal ion coordinates with eight oxygen atoms from two different crown ether rings, featuring a 1-D helical chain for complexes 5 and 6. Hence, the different sizes of alkaline metal ions exert a dramatic effect on the structural motifs of complexes 3–6. Remarkably, the dithiocarbamate moieties adopt μ2-bridging ([Au(O4NCS2)]2 and [Au(O4NCS2)]6), μ3- and μ4-bridging (1–2) and chelate forms (3–6) in the structural backbones.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/d2dt02768b</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Coordination compounds ; Coordination polymers ; Copper ; Crown ethers ; Crystals ; Heating ; Hydrogen bonding ; Lithium ions ; Metal ions ; Oxygen atoms ; Rubidium ; Silver nitrate ; Single crystals ; Sodium ; Transformations</subject><ispartof>Dalton transactions : an international journal of inorganic chemistry, 2022-11, Vol.51 (44), p.16973-16981</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Tzeng, Biing-Chiau</creatorcontrib><creatorcontrib>Chung-Lun, Wu</creatorcontrib><creatorcontrib>Jun-Wei, Hung</creatorcontrib><creatorcontrib>Su-Ying, Chien</creatorcontrib><creatorcontrib>Gene-Hsiang, Lee</creatorcontrib><title>Supramolecular assembly and structural transformation of d10-metal complexes containing (aza-15-crown-5)dithiocarbamate</title><title>Dalton transactions : an international journal of inorganic chemistry</title><description>The reaction of potassium (aza-15-crown-5)dithiocarbamate (KO4NCS2) and (Me2S)AuCl gave the dinuclear complex [Au(O4NCS2)]2, which underwent structural transformation upon heating to rearrange into the hexanuclear complex [Au(O4NCS2)]6. Under similar reaction conditions, KO4NCS2 reacted with AgNO3 or [Cu(CH3CN)4]ClO4 to give the 1-D coordination polymer [Ag(O4NCS2)]n (1) and the tetranuclear complex [Cu(O4NCS2)]4 (2), respectively. It is noted that upon heating a similar structural transformation process occurs from tetranuclear complex 2 to the octanuclear complex [Cu(O4NCS2)]8 (2′), connected by a weak Cu⋯S contact of 2.846 Å, and it has been isolated and corroborated by powder and single-crystal X-ray diffraction studies as well. Moreover, a variety of MO4NCS2 salts (M = Li+, Na+, K+ and Rb+) were used to react with AgNO3 to construct a series of coordination architectures: [LiAg(O4NCS2)2(μ-H2O)0.5]2 (3), {Na[Ag(O4NCS2)2]}n (4), {K[Ag(O4NCS2)2]}n (5) and {Rb[Ag(O4NCS2)2]}n (6). The smallest Li+ ion only coordinates with four oxygen atoms from the same azacrown ether ring and one H2O molecule, leading to a 1-D hydrogen-bonded chain with another azacrown ether ring for complex 3. The larger Na+ ion coordinates with seven oxygen atoms from two different crown ether rings, leading to a 1-D chain for complex 4. However, the largest K+ and Rb+ ions constitute a 1-D framework, except that each metal ion coordinates with eight oxygen atoms from two different crown ether rings, featuring a 1-D helical chain for complexes 5 and 6. Hence, the different sizes of alkaline metal ions exert a dramatic effect on the structural motifs of complexes 3–6. Remarkably, the dithiocarbamate moieties adopt μ2-bridging ([Au(O4NCS2)]2 and [Au(O4NCS2)]6), μ3- and μ4-bridging (1–2) and chelate forms (3–6) in the structural backbones.</description><subject>Coordination compounds</subject><subject>Coordination polymers</subject><subject>Copper</subject><subject>Crown ethers</subject><subject>Crystals</subject><subject>Heating</subject><subject>Hydrogen bonding</subject><subject>Lithium ions</subject><subject>Metal ions</subject><subject>Oxygen atoms</subject><subject>Rubidium</subject><subject>Silver nitrate</subject><subject>Single crystals</subject><subject>Sodium</subject><subject>Transformations</subject><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdj0tLAzEcxIMoWKsXP8GCl3qI5rHZ7B6l-IKCB3sv_zxWt2STmgdVP70rigdPMzA_hhmEzim5ooR314aZTJhsWnWAZrSWEneM14d_njXH6CSlLSGMEcFmaP9cdhHG4KwuDmIFKdlRuY8KvKlSjkXnEsFVOYJPfYgj5CH4KvSVoQSPNk-ZDuPO2XebJuczDH7wL9UCPgFTgXUMe4_FpRny6xA0RAVThz1FRz24ZM9-dY7Wd7fr5QNePd0_Lm9WeNdQinUruSE9NUSJmrWCdmx6SVsiBVAuNROdaYjSShnbaWXA9q3qawmNUS1Qyudo8VO7i-Gt2JQ345C0dQ68DSVtmGSdoEI03-jFP3QbSvTTuIniE9DUnPEv1-VtDQ</recordid><startdate>20221115</startdate><enddate>20221115</enddate><creator>Tzeng, Biing-Chiau</creator><creator>Chung-Lun, Wu</creator><creator>Jun-Wei, Hung</creator><creator>Su-Ying, Chien</creator><creator>Gene-Hsiang, Lee</creator><general>Royal Society of Chemistry</general><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>20221115</creationdate><title>Supramolecular assembly and structural transformation of d10-metal complexes containing (aza-15-crown-5)dithiocarbamate</title><author>Tzeng, Biing-Chiau ; Chung-Lun, Wu ; Jun-Wei, Hung ; Su-Ying, Chien ; Gene-Hsiang, Lee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p611-c873d0f1d0b5428519203918075a137c259d60bcbbde9cbdaef8bf47a6db8a113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Coordination compounds</topic><topic>Coordination polymers</topic><topic>Copper</topic><topic>Crown ethers</topic><topic>Crystals</topic><topic>Heating</topic><topic>Hydrogen bonding</topic><topic>Lithium ions</topic><topic>Metal ions</topic><topic>Oxygen atoms</topic><topic>Rubidium</topic><topic>Silver nitrate</topic><topic>Single crystals</topic><topic>Sodium</topic><topic>Transformations</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tzeng, Biing-Chiau</creatorcontrib><creatorcontrib>Chung-Lun, Wu</creatorcontrib><creatorcontrib>Jun-Wei, Hung</creatorcontrib><creatorcontrib>Su-Ying, Chien</creatorcontrib><creatorcontrib>Gene-Hsiang, Lee</creatorcontrib><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>Tzeng, Biing-Chiau</au><au>Chung-Lun, Wu</au><au>Jun-Wei, Hung</au><au>Su-Ying, Chien</au><au>Gene-Hsiang, Lee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Supramolecular assembly and structural transformation of d10-metal complexes containing (aza-15-crown-5)dithiocarbamate</atitle><jtitle>Dalton transactions : an international journal of inorganic chemistry</jtitle><date>2022-11-15</date><risdate>2022</risdate><volume>51</volume><issue>44</issue><spage>16973</spage><epage>16981</epage><pages>16973-16981</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>The reaction of potassium (aza-15-crown-5)dithiocarbamate (KO4NCS2) and (Me2S)AuCl gave the dinuclear complex [Au(O4NCS2)]2, which underwent structural transformation upon heating to rearrange into the hexanuclear complex [Au(O4NCS2)]6. Under similar reaction conditions, KO4NCS2 reacted with AgNO3 or [Cu(CH3CN)4]ClO4 to give the 1-D coordination polymer [Ag(O4NCS2)]n (1) and the tetranuclear complex [Cu(O4NCS2)]4 (2), respectively. It is noted that upon heating a similar structural transformation process occurs from tetranuclear complex 2 to the octanuclear complex [Cu(O4NCS2)]8 (2′), connected by a weak Cu⋯S contact of 2.846 Å, and it has been isolated and corroborated by powder and single-crystal X-ray diffraction studies as well. Moreover, a variety of MO4NCS2 salts (M = Li+, Na+, K+ and Rb+) were used to react with AgNO3 to construct a series of coordination architectures: [LiAg(O4NCS2)2(μ-H2O)0.5]2 (3), {Na[Ag(O4NCS2)2]}n (4), {K[Ag(O4NCS2)2]}n (5) and {Rb[Ag(O4NCS2)2]}n (6). The smallest Li+ ion only coordinates with four oxygen atoms from the same azacrown ether ring and one H2O molecule, leading to a 1-D hydrogen-bonded chain with another azacrown ether ring for complex 3. The larger Na+ ion coordinates with seven oxygen atoms from two different crown ether rings, leading to a 1-D chain for complex 4. However, the largest K+ and Rb+ ions constitute a 1-D framework, except that each metal ion coordinates with eight oxygen atoms from two different crown ether rings, featuring a 1-D helical chain for complexes 5 and 6. Hence, the different sizes of alkaline metal ions exert a dramatic effect on the structural motifs of complexes 3–6. Remarkably, the dithiocarbamate moieties adopt μ2-bridging ([Au(O4NCS2)]2 and [Au(O4NCS2)]6), μ3- and μ4-bridging (1–2) and chelate forms (3–6) in the structural backbones.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2dt02768b</doi><tpages>9</tpages></addata></record> |
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subjects | Coordination compounds Coordination polymers Copper Crown ethers Crystals Heating Hydrogen bonding Lithium ions Metal ions Oxygen atoms Rubidium Silver nitrate Single crystals Sodium Transformations |
title | Supramolecular assembly and structural transformation of d10-metal complexes containing (aza-15-crown-5)dithiocarbamate |
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