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Synthesis and luminescence properties of iridium(III) azide- and triazole-bisterpyridine complexes
We describe here the synthesis of azide-functionalised iridium(III) bisterpyridines using the "chemistry on the complex" strategy. The resulting azide-complexes are then used in the copper(I)-catalysed azide-alkyne Huisgen 1,3-dipolar cycloaddition "click chemistry" reaction to f...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2013-07, Vol.18 (8), p.8959-8975 |
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description | We describe here the synthesis of azide-functionalised iridium(III) bisterpyridines using the "chemistry on the complex" strategy. The resulting azide-complexes are then used in the copper(I)-catalysed azide-alkyne Huisgen 1,3-dipolar cycloaddition "click chemistry" reaction to from the corresponding triazole-functionalised iridium(III) bisterpyridines. The photophysical characteristics, including lifetimes, of these compounds were also investigated. Interestingly, oxygen appears to have very little effect on the lifetime of these complexes in aqueous solutions. Unexpectedly, sodium ascorbate acid appears to quench the luminescence of triazole-functionalised iridium(III) bisterpyridines, but this effect can be reversed by the addition of copper(II) sulfate, which is known to oxidize ascorbate under aerobic conditions. The results demonstrate that iridium(III) bisterpyridines can be functionalized for use in "click chemistry" facilitating the use of these photophysically interesting complexes in the modification of polymers or surfaces, to highlight just two possible applications. |
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The resulting azide-complexes are then used in the copper(I)-catalysed azide-alkyne Huisgen 1,3-dipolar cycloaddition "click chemistry" reaction to from the corresponding triazole-functionalised iridium(III) bisterpyridines. The photophysical characteristics, including lifetimes, of these compounds were also investigated. Interestingly, oxygen appears to have very little effect on the lifetime of these complexes in aqueous solutions. Unexpectedly, sodium ascorbate acid appears to quench the luminescence of triazole-functionalised iridium(III) bisterpyridines, but this effect can be reversed by the addition of copper(II) sulfate, which is known to oxidize ascorbate under aerobic conditions. The results demonstrate that iridium(III) bisterpyridines can be functionalized for use in "click chemistry" facilitating the use of these photophysically interesting complexes in the modification of polymers or surfaces, to highlight just two possible applications.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules18088959</identifier><identifier>PMID: 23896620</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aqueous solutions ; ascorbate quenching ; azide ; Azides - chemical synthesis ; Azides - chemistry ; Catalysis ; Click Chemistry ; Copper ; Copper - chemistry ; Iridium - chemistry ; iridium(III) ; Lifetime ; lifetime measurements ; Ligands ; Luminescence ; Molecular Structure ; Polymers - chemistry ; terpyridine ; Triazoles - chemical synthesis ; Triazoles - chemistry</subject><ispartof>Molecules (Basel, Switzerland), 2013-07, Vol.18 (8), p.8959-8975</ispartof><rights>Copyright MDPI AG 2013</rights><rights>2013 by the authors; licensee MDPI, Basel, Switzerland. 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-ed4111b4584feb773253226c95b426892c696467eaf8bd054663e59e29a6033f3</citedby><cites>FETCH-LOGICAL-c423t-ed4111b4584feb773253226c95b426892c696467eaf8bd054663e59e29a6033f3</cites><orcidid>0000-0002-1200-8814</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1532135603/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1532135603?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23896620$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Goldstein, Daniel C</creatorcontrib><creatorcontrib>Peterson, Joshua R</creatorcontrib><creatorcontrib>Cheng, Yuen Yap</creatorcontrib><creatorcontrib>Clady, Raphael G C</creatorcontrib><creatorcontrib>Schmidt, Timothy W</creatorcontrib><creatorcontrib>Thordarson, Pall</creatorcontrib><title>Synthesis and luminescence properties of iridium(III) azide- and triazole-bisterpyridine complexes</title><title>Molecules (Basel, Switzerland)</title><addtitle>Molecules</addtitle><description>We describe here the synthesis of azide-functionalised iridium(III) bisterpyridines using the "chemistry on the complex" strategy. The resulting azide-complexes are then used in the copper(I)-catalysed azide-alkyne Huisgen 1,3-dipolar cycloaddition "click chemistry" reaction to from the corresponding triazole-functionalised iridium(III) bisterpyridines. The photophysical characteristics, including lifetimes, of these compounds were also investigated. Interestingly, oxygen appears to have very little effect on the lifetime of these complexes in aqueous solutions. Unexpectedly, sodium ascorbate acid appears to quench the luminescence of triazole-functionalised iridium(III) bisterpyridines, but this effect can be reversed by the addition of copper(II) sulfate, which is known to oxidize ascorbate under aerobic conditions. The results demonstrate that iridium(III) bisterpyridines can be functionalized for use in "click chemistry" facilitating the use of these photophysically interesting complexes in the modification of polymers or surfaces, to highlight just two possible applications.</description><subject>Aqueous solutions</subject><subject>ascorbate quenching</subject><subject>azide</subject><subject>Azides - chemical synthesis</subject><subject>Azides - chemistry</subject><subject>Catalysis</subject><subject>Click Chemistry</subject><subject>Copper</subject><subject>Copper - chemistry</subject><subject>Iridium - chemistry</subject><subject>iridium(III)</subject><subject>Lifetime</subject><subject>lifetime measurements</subject><subject>Ligands</subject><subject>Luminescence</subject><subject>Molecular Structure</subject><subject>Polymers - chemistry</subject><subject>terpyridine</subject><subject>Triazoles - chemical synthesis</subject><subject>Triazoles - chemistry</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkk1v1DAQhi0EomXhB3BBkbiUQ8DfiS9IqOIjUqUeCmfLdiatV04c7AR1--vr7ZaqhZMt-51nZt4ZhN4S_JExhT-NMYBbA2TS4rZVQj1Dx4RTXDPM1fNH9yP0KuctxpRwIl6iI8paJSXFx8he7KblCrLPlZn6KqyjnyA7mBxUc4ozpMVDruJQ-eR7v44nXdd9qMyN76G-C1mSNzelkNr6vECad3vdBJWL4xzgGvJr9GIwIcOb-3ODfn37-vP0R312_r07_XJWO07ZUkPPCSGWi5YPYJuGUcEolU4Jy6lsFXVSSS4bMENreyy4lAyEAqqMxIwNbIO6A7ePZqvn5EeTdjoar-8eYrrUpnTjAmg8uJKGEyxZ4TTCYrCyIHmjBtJTVlifD6x5tSP0xY8lmfAE-vRn8lf6Mv7RkjaYc1EAJ_eAFH-vkBc9-mJrCGaCuGZdBiGl4oy3Rfr-H-k2rmkqVmlSLCBM7PvbIHJQuRRzTjA8FEOw3m-D_m8bSsy7x108RPwdP7sFOUGyRA</recordid><startdate>20130726</startdate><enddate>20130726</enddate><creator>Goldstein, Daniel C</creator><creator>Peterson, Joshua R</creator><creator>Cheng, Yuen Yap</creator><creator>Clady, Raphael G C</creator><creator>Schmidt, Timothy W</creator><creator>Thordarson, Pall</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-1200-8814</orcidid></search><sort><creationdate>20130726</creationdate><title>Synthesis and luminescence properties of iridium(III) azide- and triazole-bisterpyridine complexes</title><author>Goldstein, Daniel C ; Peterson, Joshua R ; Cheng, Yuen Yap ; Clady, Raphael G C ; Schmidt, Timothy W ; Thordarson, Pall</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-ed4111b4584feb773253226c95b426892c696467eaf8bd054663e59e29a6033f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Aqueous solutions</topic><topic>ascorbate quenching</topic><topic>azide</topic><topic>Azides - chemical synthesis</topic><topic>Azides - chemistry</topic><topic>Catalysis</topic><topic>Click Chemistry</topic><topic>Copper</topic><topic>Copper - chemistry</topic><topic>Iridium - chemistry</topic><topic>iridium(III)</topic><topic>Lifetime</topic><topic>lifetime measurements</topic><topic>Ligands</topic><topic>Luminescence</topic><topic>Molecular Structure</topic><topic>Polymers - chemistry</topic><topic>terpyridine</topic><topic>Triazoles - chemical synthesis</topic><topic>Triazoles - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Goldstein, Daniel C</creatorcontrib><creatorcontrib>Peterson, Joshua R</creatorcontrib><creatorcontrib>Cheng, Yuen Yap</creatorcontrib><creatorcontrib>Clady, Raphael G C</creatorcontrib><creatorcontrib>Schmidt, Timothy W</creatorcontrib><creatorcontrib>Thordarson, Pall</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Goldstein, Daniel C</au><au>Peterson, Joshua R</au><au>Cheng, Yuen Yap</au><au>Clady, Raphael G C</au><au>Schmidt, Timothy W</au><au>Thordarson, Pall</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and luminescence properties of iridium(III) azide- and triazole-bisterpyridine complexes</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><addtitle>Molecules</addtitle><date>2013-07-26</date><risdate>2013</risdate><volume>18</volume><issue>8</issue><spage>8959</spage><epage>8975</epage><pages>8959-8975</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>We describe here the synthesis of azide-functionalised iridium(III) bisterpyridines using the "chemistry on the complex" strategy. The resulting azide-complexes are then used in the copper(I)-catalysed azide-alkyne Huisgen 1,3-dipolar cycloaddition "click chemistry" reaction to from the corresponding triazole-functionalised iridium(III) bisterpyridines. The photophysical characteristics, including lifetimes, of these compounds were also investigated. Interestingly, oxygen appears to have very little effect on the lifetime of these complexes in aqueous solutions. Unexpectedly, sodium ascorbate acid appears to quench the luminescence of triazole-functionalised iridium(III) bisterpyridines, but this effect can be reversed by the addition of copper(II) sulfate, which is known to oxidize ascorbate under aerobic conditions. The results demonstrate that iridium(III) bisterpyridines can be functionalized for use in "click chemistry" facilitating the use of these photophysically interesting complexes in the modification of polymers or surfaces, to highlight just two possible applications.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>23896620</pmid><doi>10.3390/molecules18088959</doi><tpages>17</tpages><orcidid>https://orcid.org/0000-0002-1200-8814</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aqueous solutions ascorbate quenching azide Azides - chemical synthesis Azides - chemistry Catalysis Click Chemistry Copper Copper - chemistry Iridium - chemistry iridium(III) Lifetime lifetime measurements Ligands Luminescence Molecular Structure Polymers - chemistry terpyridine Triazoles - chemical synthesis Triazoles - chemistry |
title | Synthesis and luminescence properties of iridium(III) azide- and triazole-bisterpyridine complexes |
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