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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
Main Authors: Tzeng, Biing-Chiau, Chung-Lun, Wu, Jun-Wei, Hung, Su-Ying, Chien, Gene-Hsiang, Lee
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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.
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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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source Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list)
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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