Synchronized biphotonic process triggering CC coupling catalytic reactions
[Display omitted] •Visible-light photocatalytic reactions are widely desirable.•Activation of aryl(Ar)-halides by visible-light is found to be a challenging task.•Photon upconversion based on TTA enables CC coupling catalytic reactions. Activation of aryl(Ar)-halides for CC coupling catalytic reacti...
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Veröffentlicht in: | Applied catalysis. B, Environmental Environmental, 2018-12, Vol.237, p.18-23 |
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container_title | Applied catalysis. B, Environmental |
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creator | López-Calixto, Carmen G. Liras, Marta de la Peña O’Shea, Victor A. Pérez-Ruiz, Raúl |
description | [Display omitted]
•Visible-light photocatalytic reactions are widely desirable.•Activation of aryl(Ar)-halides by visible-light is found to be a challenging task.•Photon upconversion based on TTA enables CC coupling catalytic reactions.
Activation of aryl(Ar)-halides for CC coupling catalytic reactions using visible light has become one of the most challenging tasks in organic synthesis since it offers effective and safer alternatives to traditional dehalogenation protocols. The insufficient energy provided by visible light to cleave such strong CH alogen bonds certainly makes necessary the development of new protocols to overcome this limitation. We report here the application of photon upconversion (UC) technology based on triplet-triplet annihilation (TTA) to a CC coupling catalytic reaction, a possibility that has not been investigated to date. This synchronized biphotonic process (TTA-UC) activates successfully Ar-halides with visible light. Based on product analysis and spectroscopic experiments, a cascade process combining photophysical and photochemical steps is proposed for the mechanism rationalization. Visible light, ambient temperature and pressure, low-loading metal-free photocatalysts and no additives make this protocol very attractive for applications to the synthesis of fine chemical building blocks, pharmaceuticals, agrochemicals or new materials. |
doi_str_mv | 10.1016/j.apcatb.2018.05.062 |
format | Article |
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•Visible-light photocatalytic reactions are widely desirable.•Activation of aryl(Ar)-halides by visible-light is found to be a challenging task.•Photon upconversion based on TTA enables CC coupling catalytic reactions.
Activation of aryl(Ar)-halides for CC coupling catalytic reactions using visible light has become one of the most challenging tasks in organic synthesis since it offers effective and safer alternatives to traditional dehalogenation protocols. The insufficient energy provided by visible light to cleave such strong CH alogen bonds certainly makes necessary the development of new protocols to overcome this limitation. We report here the application of photon upconversion (UC) technology based on triplet-triplet annihilation (TTA) to a CC coupling catalytic reaction, a possibility that has not been investigated to date. This synchronized biphotonic process (TTA-UC) activates successfully Ar-halides with visible light. Based on product analysis and spectroscopic experiments, a cascade process combining photophysical and photochemical steps is proposed for the mechanism rationalization. Visible light, ambient temperature and pressure, low-loading metal-free photocatalysts and no additives make this protocol very attractive for applications to the synthesis of fine chemical building blocks, pharmaceuticals, agrochemicals or new materials.</description><identifier>ISSN: 0926-3373</identifier><identifier>EISSN: 1873-3883</identifier><identifier>DOI: 10.1016/j.apcatb.2018.05.062</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Additives ; Agrochemicals ; Alternative energy sources ; Ambient temperature ; Aromatic compounds ; Atoms & subatomic particles ; Bonding strength ; C[sbnd]C coupling ; Catalysis ; Chemical bonds ; Chemical synthesis ; Continuous-flow ; Coupling ; Dehalogenation ; Electron transfer catalysis ; Electron transfer reactions ; Fine chemicals ; Halides ; Metal-free photocatalysts ; Organic chemistry ; Photocatalysis ; Photochemicals ; Upconversion ; Visible light</subject><ispartof>Applied catalysis. B, Environmental, 2018-12, Vol.237, p.18-23</ispartof><rights>2018 The Authors</rights><rights>Copyright Elsevier BV Dec 5, 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.apcatb.2018.05.062$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>López-Calixto, Carmen G.</creatorcontrib><creatorcontrib>Liras, Marta</creatorcontrib><creatorcontrib>de la Peña O’Shea, Victor A.</creatorcontrib><creatorcontrib>Pérez-Ruiz, Raúl</creatorcontrib><title>Synchronized biphotonic process triggering CC coupling catalytic reactions</title><title>Applied catalysis. B, Environmental</title><description>[Display omitted]
•Visible-light photocatalytic reactions are widely desirable.•Activation of aryl(Ar)-halides by visible-light is found to be a challenging task.•Photon upconversion based on TTA enables CC coupling catalytic reactions.
Activation of aryl(Ar)-halides for CC coupling catalytic reactions using visible light has become one of the most challenging tasks in organic synthesis since it offers effective and safer alternatives to traditional dehalogenation protocols. The insufficient energy provided by visible light to cleave such strong CH alogen bonds certainly makes necessary the development of new protocols to overcome this limitation. We report here the application of photon upconversion (UC) technology based on triplet-triplet annihilation (TTA) to a CC coupling catalytic reaction, a possibility that has not been investigated to date. This synchronized biphotonic process (TTA-UC) activates successfully Ar-halides with visible light. Based on product analysis and spectroscopic experiments, a cascade process combining photophysical and photochemical steps is proposed for the mechanism rationalization. Visible light, ambient temperature and pressure, low-loading metal-free photocatalysts and no additives make this protocol very attractive for applications to the synthesis of fine chemical building blocks, pharmaceuticals, agrochemicals or new materials.</description><subject>Additives</subject><subject>Agrochemicals</subject><subject>Alternative energy sources</subject><subject>Ambient temperature</subject><subject>Aromatic compounds</subject><subject>Atoms & subatomic particles</subject><subject>Bonding strength</subject><subject>C[sbnd]C coupling</subject><subject>Catalysis</subject><subject>Chemical bonds</subject><subject>Chemical synthesis</subject><subject>Continuous-flow</subject><subject>Coupling</subject><subject>Dehalogenation</subject><subject>Electron transfer catalysis</subject><subject>Electron transfer reactions</subject><subject>Fine chemicals</subject><subject>Halides</subject><subject>Metal-free photocatalysts</subject><subject>Organic chemistry</subject><subject>Photocatalysis</subject><subject>Photochemicals</subject><subject>Upconversion</subject><subject>Visible light</subject><issn>0926-3373</issn><issn>1873-3883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNotkEFLAzEQhYMoWKv_wMOC510nmWw2vQiyaFUKHuw97KazbZayuyapUH-9KfUwzAw83nt8jN1zKDhw9dgXzWSb2BYCuC6gLECJCzbjusIctcZLNoOFUDlihdfsJoQeAAQKPWMfX8fB7vw4uF_aZK2bdmNMj80mP1oKIYvebbfk3bDN6jqz42Han-4U1-yPMQk9NTa6cQi37Kpr9oHu_vecrV9f1vVbvvpcvtfPq5w08rztOqpQyhYaxUnKShEoqWW1QCXQ0qYT2AlpW7RlZ1utSsVh0VUtEkEpNM7Zw9k2Nfw-UIimHw9-SIlGcC7TKMGT6umsotTkx5E3wToakr_zZKPZjM5wMCd8pjdnfOaEz0BpEj78A1fjZkc</recordid><startdate>20181205</startdate><enddate>20181205</enddate><creator>López-Calixto, Carmen G.</creator><creator>Liras, Marta</creator><creator>de la Peña O’Shea, Victor A.</creator><creator>Pérez-Ruiz, Raúl</creator><general>Elsevier B.V</general><general>Elsevier BV</general><scope>6I.</scope><scope>AAFTH</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>JG9</scope><scope>KR7</scope><scope>L7M</scope><scope>SOI</scope></search><sort><creationdate>20181205</creationdate><title>Synchronized biphotonic process triggering CC coupling catalytic reactions</title><author>López-Calixto, Carmen G. ; Liras, Marta ; de la Peña O’Shea, Victor A. ; Pérez-Ruiz, Raúl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e831-bffe7344b0a61e4476e06484793623cedf23f24cb3c5fcb8656109f7b3ee05283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Additives</topic><topic>Agrochemicals</topic><topic>Alternative energy sources</topic><topic>Ambient temperature</topic><topic>Aromatic compounds</topic><topic>Atoms & subatomic particles</topic><topic>Bonding strength</topic><topic>C[sbnd]C coupling</topic><topic>Catalysis</topic><topic>Chemical bonds</topic><topic>Chemical synthesis</topic><topic>Continuous-flow</topic><topic>Coupling</topic><topic>Dehalogenation</topic><topic>Electron transfer catalysis</topic><topic>Electron transfer reactions</topic><topic>Fine chemicals</topic><topic>Halides</topic><topic>Metal-free photocatalysts</topic><topic>Organic chemistry</topic><topic>Photocatalysis</topic><topic>Photochemicals</topic><topic>Upconversion</topic><topic>Visible light</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>López-Calixto, Carmen G.</creatorcontrib><creatorcontrib>Liras, Marta</creatorcontrib><creatorcontrib>de la Peña O’Shea, Victor A.</creatorcontrib><creatorcontrib>Pérez-Ruiz, Raúl</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Civil Engineering Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Applied catalysis. B, Environmental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>López-Calixto, Carmen G.</au><au>Liras, Marta</au><au>de la Peña O’Shea, Victor A.</au><au>Pérez-Ruiz, Raúl</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synchronized biphotonic process triggering CC coupling catalytic reactions</atitle><jtitle>Applied catalysis. B, Environmental</jtitle><date>2018-12-05</date><risdate>2018</risdate><volume>237</volume><spage>18</spage><epage>23</epage><pages>18-23</pages><issn>0926-3373</issn><eissn>1873-3883</eissn><abstract>[Display omitted]
•Visible-light photocatalytic reactions are widely desirable.•Activation of aryl(Ar)-halides by visible-light is found to be a challenging task.•Photon upconversion based on TTA enables CC coupling catalytic reactions.
Activation of aryl(Ar)-halides for CC coupling catalytic reactions using visible light has become one of the most challenging tasks in organic synthesis since it offers effective and safer alternatives to traditional dehalogenation protocols. The insufficient energy provided by visible light to cleave such strong CH alogen bonds certainly makes necessary the development of new protocols to overcome this limitation. We report here the application of photon upconversion (UC) technology based on triplet-triplet annihilation (TTA) to a CC coupling catalytic reaction, a possibility that has not been investigated to date. This synchronized biphotonic process (TTA-UC) activates successfully Ar-halides with visible light. Based on product analysis and spectroscopic experiments, a cascade process combining photophysical and photochemical steps is proposed for the mechanism rationalization. Visible light, ambient temperature and pressure, low-loading metal-free photocatalysts and no additives make this protocol very attractive for applications to the synthesis of fine chemical building blocks, pharmaceuticals, agrochemicals or new materials.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/j.apcatb.2018.05.062</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Additives Agrochemicals Alternative energy sources Ambient temperature Aromatic compounds Atoms & subatomic particles Bonding strength C[sbnd]C coupling Catalysis Chemical bonds Chemical synthesis Continuous-flow Coupling Dehalogenation Electron transfer catalysis Electron transfer reactions Fine chemicals Halides Metal-free photocatalysts Organic chemistry Photocatalysis Photochemicals Upconversion Visible light |
title | Synchronized biphotonic process triggering CC coupling catalytic reactions |
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