Construction of Two 3D Homochiral Frameworks with 1D Chiral Pores via Chiral Recognition
The reactions of a pair of enantiomers of macrocyclic nickel(II) complexes with racemic penicillamine generated two 3D hydrogen-bonded homochiral frameworks of {[Ni(f-(SS)-L)]2(l-pends)(ClO4)2} n (Λ-1) and {[Ni(f-(RR)-L)]2(d-pends) (ClO4)2} n (Δ-1). The frameworks possess 1D tubular pores and opposi...
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Veröffentlicht in: | Inorganic chemistry 2011-04, Vol.50 (8), p.3177-3179 |
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creator | Li, Huan-Yong Jiang, Long Xiang, Hua Makal, Tegan A. Zhou, Hong-Cai Lu, Tong-Bu |
description | The reactions of a pair of enantiomers of macrocyclic nickel(II) complexes with racemic penicillamine generated two 3D hydrogen-bonded homochiral frameworks of {[Ni(f-(SS)-L)]2(l-pends)(ClO4)2} n (Λ-1) and {[Ni(f-(RR)-L)]2(d-pends) (ClO4)2} n (Δ-1). The frameworks possess 1D tubular pores and opposite right/left-handed helical porous surfaces (L = 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane; pends2− = penicillaminedisulfide anion). |
doi_str_mv | 10.1021/ic200264s |
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The frameworks possess 1D tubular pores and opposite right/left-handed helical porous surfaces (L = 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane; pends2− = penicillaminedisulfide anion).</description><identifier>ISSN: 0020-1669</identifier><identifier>ISSN: 1520-510X</identifier><identifier>EISSN: 1520-510X</identifier><identifier>DOI: 10.1021/ic200264s</identifier><identifier>PMID: 21434680</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>Inorganic chemistry, 2011-04, Vol.50 (8), p.3177-3179</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a314t-a41da41efc8270ed6ec217edb2a81a1e84659a991742dee6c88e6de1a76669e53</citedby><cites>FETCH-LOGICAL-a314t-a41da41efc8270ed6ec217edb2a81a1e84659a991742dee6c88e6de1a76669e53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ic200264s$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ic200264s$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21434680$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Huan-Yong</creatorcontrib><creatorcontrib>Jiang, Long</creatorcontrib><creatorcontrib>Xiang, Hua</creatorcontrib><creatorcontrib>Makal, Tegan A.</creatorcontrib><creatorcontrib>Zhou, Hong-Cai</creatorcontrib><creatorcontrib>Lu, Tong-Bu</creatorcontrib><title>Construction of Two 3D Homochiral Frameworks with 1D Chiral Pores via Chiral Recognition</title><title>Inorganic chemistry</title><addtitle>Inorg. 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The frameworks possess 1D tubular pores and opposite right/left-handed helical porous surfaces (L = 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane; pends2− = penicillaminedisulfide anion).</description><issn>0020-1669</issn><issn>1520-510X</issn><issn>1520-510X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNptkEFLw0AQhRdRbK0e_AOyFxEP0Z3NZpMcJbVWKChSobew3UxsapKtu4nFf29KbE8ehhnefDx4j5BLYHfAONwXmjPGpXBHZAgBZ14AbHFMhp3IPJAyHpAz59aMsdgX8pQMOIjuiNiQLBJTu8a2uilMTU1O51tD_TGdmsroVWFVSSdWVbg19tPRbdGsKIxp0n9ejUVHvwu1F95Qm4-62Hmdk5NclQ4v_vaIvE8e58nUm708PScPM0_5IBpPCci6wVxHPGSYSdQcQsyWXEWgACMhg1jFMYSCZ4hSRxHKDEGFssuFgT8iN73vxpqvFl2TVoXTWJaqRtO6NJIQxlxIvyNve1Jb45zFPN3YolL2JwWW7npMDz127NWfa7usMDuQ--I64LoHlHbp2rS27kL-Y_QL4515DA</recordid><startdate>20110418</startdate><enddate>20110418</enddate><creator>Li, Huan-Yong</creator><creator>Jiang, Long</creator><creator>Xiang, Hua</creator><creator>Makal, Tegan A.</creator><creator>Zhou, Hong-Cai</creator><creator>Lu, Tong-Bu</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110418</creationdate><title>Construction of Two 3D Homochiral Frameworks with 1D Chiral Pores via Chiral Recognition</title><author>Li, Huan-Yong ; Jiang, Long ; Xiang, Hua ; Makal, Tegan A. ; Zhou, Hong-Cai ; Lu, Tong-Bu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a314t-a41da41efc8270ed6ec217edb2a81a1e84659a991742dee6c88e6de1a76669e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Huan-Yong</creatorcontrib><creatorcontrib>Jiang, Long</creatorcontrib><creatorcontrib>Xiang, Hua</creatorcontrib><creatorcontrib>Makal, Tegan A.</creatorcontrib><creatorcontrib>Zhou, Hong-Cai</creatorcontrib><creatorcontrib>Lu, Tong-Bu</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>Li, Huan-Yong</au><au>Jiang, Long</au><au>Xiang, Hua</au><au>Makal, Tegan A.</au><au>Zhou, Hong-Cai</au><au>Lu, Tong-Bu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Construction of Two 3D Homochiral Frameworks with 1D Chiral Pores via Chiral Recognition</atitle><jtitle>Inorganic chemistry</jtitle><addtitle>Inorg. Chem</addtitle><date>2011-04-18</date><risdate>2011</risdate><volume>50</volume><issue>8</issue><spage>3177</spage><epage>3179</epage><pages>3177-3179</pages><issn>0020-1669</issn><issn>1520-510X</issn><eissn>1520-510X</eissn><abstract>The reactions of a pair of enantiomers of macrocyclic nickel(II) complexes with racemic penicillamine generated two 3D hydrogen-bonded homochiral frameworks of {[Ni(f-(SS)-L)]2(l-pends)(ClO4)2} n (Λ-1) and {[Ni(f-(RR)-L)]2(d-pends) (ClO4)2} n (Δ-1). The frameworks possess 1D tubular pores and opposite right/left-handed helical porous surfaces (L = 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane; pends2− = penicillaminedisulfide anion).</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>21434680</pmid><doi>10.1021/ic200264s</doi><tpages>3</tpages></addata></record> |
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title | Construction of Two 3D Homochiral Frameworks with 1D Chiral Pores via Chiral Recognition |
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