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Optical Resolution of the Water-Soluble Ti4(embonate)6 Cages for Enantioselective Recognition of Chiral Drugs
Synergetic optical resolution and chiral amplification of tetrahedral Ti4L6 cages by enantiopure coordination cations have been realized in this work. Anionic ΔΔΔΔ-[Ti4L6] and ΛΛΛΛ-[Ti4L6] cages (L = embonate) have been completely resolved by enantiopure Λ-[Mn(1R,2R-DCH)3] and Δ-[Mn(1S,2S-DCH)3] c...
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Published in: | Chemistry of materials 2018-11, Vol.30 (21), p.7769-7775 |
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container_title | Chemistry of materials |
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creator | He, Yan-Ping Yuan, Lv-Bing Song, Jin-Shuai Chen, Guang-Hui Lin, Qipu Li, Chunsen Zhang, Lei Zhang, Jian |
description | Synergetic optical resolution and chiral amplification of tetrahedral Ti4L6 cages by enantiopure coordination cations have been realized in this work. Anionic ΔΔΔΔ-[Ti4L6] and ΛΛΛΛ-[Ti4L6] cages (L = embonate) have been completely resolved by enantiopure Λ-[Mn(1R,2R-DCH)3] and Δ-[Mn(1S,2S-DCH)3] cations, respectively. Accordingly, two homochiral compounds (PTC-108(Δ) and PTC-108(Λ)) with three-dimensional supramolecular architectures were formed, containing larger diamondoid cages. Such an unusual resolution process clearly shows the stepwise transfer of homochirality from an enantiopure molecule to a resolved hydrogen-bonding aggregation and a final homochiral framework. Moreover, the separated homochiral Ti4L6 cage presents enantioselective recognition toward chiral organic and pharmaceutical molecules. This work opens a novel resolution-dependent homochiral framework construction approach, and it also takes the homochiral tetrahedral Ti4L6 cages with high solubility and stability into promising enantioselective application. |
doi_str_mv | 10.1021/acs.chemmater.8b03174 |
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Anionic ΔΔΔΔ-[Ti4L6] and ΛΛΛΛ-[Ti4L6] cages (L = embonate) have been completely resolved by enantiopure Λ-[Mn(1R,2R-DCH)3] and Δ-[Mn(1S,2S-DCH)3] cations, respectively. Accordingly, two homochiral compounds (PTC-108(Δ) and PTC-108(Λ)) with three-dimensional supramolecular architectures were formed, containing larger diamondoid cages. Such an unusual resolution process clearly shows the stepwise transfer of homochirality from an enantiopure molecule to a resolved hydrogen-bonding aggregation and a final homochiral framework. Moreover, the separated homochiral Ti4L6 cage presents enantioselective recognition toward chiral organic and pharmaceutical molecules. This work opens a novel resolution-dependent homochiral framework construction approach, and it also takes the homochiral tetrahedral Ti4L6 cages with high solubility and stability into promising enantioselective application.</description><identifier>ISSN: 0897-4756</identifier><identifier>EISSN: 1520-5002</identifier><identifier>DOI: 10.1021/acs.chemmater.8b03174</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>Chemistry of materials, 2018-11, Vol.30 (21), p.7769-7775</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-7720-4667 ; 0000-0002-7723-3676 ; 0000-0003-3373-9621</orcidid></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>He, Yan-Ping</creatorcontrib><creatorcontrib>Yuan, Lv-Bing</creatorcontrib><creatorcontrib>Song, Jin-Shuai</creatorcontrib><creatorcontrib>Chen, Guang-Hui</creatorcontrib><creatorcontrib>Lin, Qipu</creatorcontrib><creatorcontrib>Li, Chunsen</creatorcontrib><creatorcontrib>Zhang, Lei</creatorcontrib><creatorcontrib>Zhang, Jian</creatorcontrib><title>Optical Resolution of the Water-Soluble Ti4(embonate)6 Cages for Enantioselective Recognition of Chiral Drugs</title><title>Chemistry of materials</title><addtitle>Chem. 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Mater</addtitle><date>2018-11-13</date><risdate>2018</risdate><volume>30</volume><issue>21</issue><spage>7769</spage><epage>7775</epage><pages>7769-7775</pages><issn>0897-4756</issn><eissn>1520-5002</eissn><abstract>Synergetic optical resolution and chiral amplification of tetrahedral Ti4L6 cages by enantiopure coordination cations have been realized in this work. Anionic ΔΔΔΔ-[Ti4L6] and ΛΛΛΛ-[Ti4L6] cages (L = embonate) have been completely resolved by enantiopure Λ-[Mn(1R,2R-DCH)3] and Δ-[Mn(1S,2S-DCH)3] cations, respectively. Accordingly, two homochiral compounds (PTC-108(Δ) and PTC-108(Λ)) with three-dimensional supramolecular architectures were formed, containing larger diamondoid cages. Such an unusual resolution process clearly shows the stepwise transfer of homochirality from an enantiopure molecule to a resolved hydrogen-bonding aggregation and a final homochiral framework. Moreover, the separated homochiral Ti4L6 cage presents enantioselective recognition toward chiral organic and pharmaceutical molecules. This work opens a novel resolution-dependent homochiral framework construction approach, and it also takes the homochiral tetrahedral Ti4L6 cages with high solubility and stability into promising enantioselective application.</abstract><pub>American Chemical Society</pub><doi>10.1021/acs.chemmater.8b03174</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-7720-4667</orcidid><orcidid>https://orcid.org/0000-0002-7723-3676</orcidid><orcidid>https://orcid.org/0000-0003-3373-9621</orcidid></addata></record> |
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title | Optical Resolution of the Water-Soluble Ti4(embonate)6 Cages for Enantioselective Recognition of Chiral Drugs |
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