Shape persistent hybrid dendrimers from benzene and triazole via ‘click chemistry’
Fully aromatic rigid dendrimers have been synthesized at room temperature based on two different ‘click’-reactions: The dendronization was carried out via the copper catalyzed azide–alkyne Huisgen cycloaddition or Diels–Alder cycloaddition, respectively. The feasible combination of both reactions le...
Gespeichert in:
| Veröffentlicht in: | Tetrahedron 2014-05, Vol.70 (19), p.3178-3184 |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 3184 |
|---|---|
| container_issue | 19 |
| container_start_page | 3178 |
| container_title | Tetrahedron |
| container_volume | 70 |
| creator | Stangenberg, René Türp, David Müllen, Klaus |
| description | Fully aromatic rigid dendrimers have been synthesized at room temperature based on two different ‘click’-reactions: The dendronization was carried out via the copper catalyzed azide–alkyne Huisgen cycloaddition or Diels–Alder cycloaddition, respectively. The feasible combination of both reactions leads to dendrimer hybrids. Stiff aromatic dendrimers, whose highly nitrogen containing scaffolds are solely based on interconnected benzene and triazole rings, were created.
[Display omitted] |
| doi_str_mv | 10.1016/j.tet.2014.03.037 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1744684089</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0040402014003718</els_id><sourcerecordid>1744684089</sourcerecordid><originalsourceid>FETCH-LOGICAL-c330t-439dd1d7c36f956ae9881c51ef1a1f270d13ba4d3a084cc42fb4caccb38037be3</originalsourceid><addsrcrecordid>eNp9UMtKA0EQHETBGP0Ab3P0srF7Z7IPPEnwBQEPPq7D7EwvmbjZjTMbITnlM_T38iVOiGehoKCpKrqKsUuEEQJm1_NRT_0oBZQjEBH5ERugzGQylpgdswGAhERCCqfsLIQ5ACCmYsDeX2Z6SXxJPrjQU9vz2bryznJLrfVuEe-89t2CV9RuqCWuW8t77_Sma4h_Oc1322_TOPPBzYwWMcOvd9ufc3ZS6ybQxR8P2dv93evkMZk-PzxNbqeJEQL6RIrSWrS5EVldjjNNZVGgGSPVqLFOc7AoKi2t0FBIY2RaV9JoYypRxIoViSG7OuQuffe5otCr-IKhptEtdaugMJcyKyQUZZTiQWp8F4KnWi1jP-3XCkHtN1RzFTdU-w0ViIg8em4OHoodvhx5FYyj1pB1nkyvbOf-cf8C8Yd9Jw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1744684089</pqid></control><display><type>article</type><title>Shape persistent hybrid dendrimers from benzene and triazole via ‘click chemistry’</title><source>Elsevier ScienceDirect Journals</source><creator>Stangenberg, René ; Türp, David ; Müllen, Klaus</creator><creatorcontrib>Stangenberg, René ; Türp, David ; Müllen, Klaus</creatorcontrib><description>Fully aromatic rigid dendrimers have been synthesized at room temperature based on two different ‘click’-reactions: The dendronization was carried out via the copper catalyzed azide–alkyne Huisgen cycloaddition or Diels–Alder cycloaddition, respectively. The feasible combination of both reactions leads to dendrimer hybrids. Stiff aromatic dendrimers, whose highly nitrogen containing scaffolds are solely based on interconnected benzene and triazole rings, were created.
[Display omitted]</description><identifier>ISSN: 0040-4020</identifier><identifier>EISSN: 1464-5416</identifier><identifier>DOI: 10.1016/j.tet.2014.03.037</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Benzene ; Click chemistry ; Copper ; Cycloaddition ; Dendrimer ; Dendrimers ; Polyphenylene ; Scaffolds ; Synthesis ; Tetrahedrons ; Triazole ; Triazoles</subject><ispartof>Tetrahedron, 2014-05, Vol.70 (19), p.3178-3184</ispartof><rights>2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c330t-439dd1d7c36f956ae9881c51ef1a1f270d13ba4d3a084cc42fb4caccb38037be3</citedby><cites>FETCH-LOGICAL-c330t-439dd1d7c36f956ae9881c51ef1a1f270d13ba4d3a084cc42fb4caccb38037be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0040402014003718$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids></links><search><creatorcontrib>Stangenberg, René</creatorcontrib><creatorcontrib>Türp, David</creatorcontrib><creatorcontrib>Müllen, Klaus</creatorcontrib><title>Shape persistent hybrid dendrimers from benzene and triazole via ‘click chemistry’</title><title>Tetrahedron</title><description>Fully aromatic rigid dendrimers have been synthesized at room temperature based on two different ‘click’-reactions: The dendronization was carried out via the copper catalyzed azide–alkyne Huisgen cycloaddition or Diels–Alder cycloaddition, respectively. The feasible combination of both reactions leads to dendrimer hybrids. Stiff aromatic dendrimers, whose highly nitrogen containing scaffolds are solely based on interconnected benzene and triazole rings, were created.
[Display omitted]</description><subject>Benzene</subject><subject>Click chemistry</subject><subject>Copper</subject><subject>Cycloaddition</subject><subject>Dendrimer</subject><subject>Dendrimers</subject><subject>Polyphenylene</subject><subject>Scaffolds</subject><subject>Synthesis</subject><subject>Tetrahedrons</subject><subject>Triazole</subject><subject>Triazoles</subject><issn>0040-4020</issn><issn>1464-5416</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp9UMtKA0EQHETBGP0Ab3P0srF7Z7IPPEnwBQEPPq7D7EwvmbjZjTMbITnlM_T38iVOiGehoKCpKrqKsUuEEQJm1_NRT_0oBZQjEBH5ERugzGQylpgdswGAhERCCqfsLIQ5ACCmYsDeX2Z6SXxJPrjQU9vz2bryznJLrfVuEe-89t2CV9RuqCWuW8t77_Sma4h_Oc1322_TOPPBzYwWMcOvd9ufc3ZS6ybQxR8P2dv93evkMZk-PzxNbqeJEQL6RIrSWrS5EVldjjNNZVGgGSPVqLFOc7AoKi2t0FBIY2RaV9JoYypRxIoViSG7OuQuffe5otCr-IKhptEtdaugMJcyKyQUZZTiQWp8F4KnWi1jP-3XCkHtN1RzFTdU-w0ViIg8em4OHoodvhx5FYyj1pB1nkyvbOf-cf8C8Yd9Jw</recordid><startdate>20140513</startdate><enddate>20140513</enddate><creator>Stangenberg, René</creator><creator>Türp, David</creator><creator>Müllen, Klaus</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20140513</creationdate><title>Shape persistent hybrid dendrimers from benzene and triazole via ‘click chemistry’</title><author>Stangenberg, René ; Türp, David ; Müllen, Klaus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c330t-439dd1d7c36f956ae9881c51ef1a1f270d13ba4d3a084cc42fb4caccb38037be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Benzene</topic><topic>Click chemistry</topic><topic>Copper</topic><topic>Cycloaddition</topic><topic>Dendrimer</topic><topic>Dendrimers</topic><topic>Polyphenylene</topic><topic>Scaffolds</topic><topic>Synthesis</topic><topic>Tetrahedrons</topic><topic>Triazole</topic><topic>Triazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Stangenberg, René</creatorcontrib><creatorcontrib>Türp, David</creatorcontrib><creatorcontrib>Müllen, Klaus</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Tetrahedron</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Stangenberg, René</au><au>Türp, David</au><au>Müllen, Klaus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Shape persistent hybrid dendrimers from benzene and triazole via ‘click chemistry’</atitle><jtitle>Tetrahedron</jtitle><date>2014-05-13</date><risdate>2014</risdate><volume>70</volume><issue>19</issue><spage>3178</spage><epage>3184</epage><pages>3178-3184</pages><issn>0040-4020</issn><eissn>1464-5416</eissn><abstract>Fully aromatic rigid dendrimers have been synthesized at room temperature based on two different ‘click’-reactions: The dendronization was carried out via the copper catalyzed azide–alkyne Huisgen cycloaddition or Diels–Alder cycloaddition, respectively. The feasible combination of both reactions leads to dendrimer hybrids. Stiff aromatic dendrimers, whose highly nitrogen containing scaffolds are solely based on interconnected benzene and triazole rings, were created.
[Display omitted]</abstract><pub>Elsevier Ltd</pub><doi>10.1016/j.tet.2014.03.037</doi><tpages>7</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0040-4020 |
| ispartof | Tetrahedron, 2014-05, Vol.70 (19), p.3178-3184 |
| issn | 0040-4020 1464-5416 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_1744684089 |
| source | Elsevier ScienceDirect Journals |
| subjects | Benzene Click chemistry Copper Cycloaddition Dendrimer Dendrimers Polyphenylene Scaffolds Synthesis Tetrahedrons Triazole Triazoles |
| title | Shape persistent hybrid dendrimers from benzene and triazole via ‘click chemistry’ |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T22%3A15%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Shape%20persistent%20hybrid%20dendrimers%20from%20benzene%20and%20triazole%20via%20%E2%80%98click%20chemistry%E2%80%99&rft.jtitle=Tetrahedron&rft.au=Stangenberg,%20Ren%C3%A9&rft.date=2014-05-13&rft.volume=70&rft.issue=19&rft.spage=3178&rft.epage=3184&rft.pages=3178-3184&rft.issn=0040-4020&rft.eissn=1464-5416&rft_id=info:doi/10.1016/j.tet.2014.03.037&rft_dat=%3Cproquest_cross%3E1744684089%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1744684089&rft_id=info:pmid/&rft_els_id=S0040402014003718&rfr_iscdi=true |