N-Heterocyclic carbenes (NHCs) as organocatalysts and structural components in metal-free polymer synthesis
The chemistry of N -heterocyclic carbenes (NHCs) has witnessed tremendous development in the past two decades: NHCs have not only become versatile ligands for transition metals, but have also emerged as powerful organic catalysts in molecular chemistry and, more recently, in metal-free polymer synth...
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Veröffentlicht in: | Chemical Society reviews 2013-01, Vol.42 (5), p.2142-2172 |
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description | The chemistry of
N
-heterocyclic carbenes (NHCs) has witnessed tremendous development in the past two decades: NHCs have not only become versatile ligands for transition metals, but have also emerged as powerful organic catalysts in molecular chemistry and, more recently, in metal-free polymer synthesis. To understand the success of NHCs, this review first presents the electronic properties of NHCs, their main synthetic methods, their handling, and their reactivity. Their ability to activate key functional groups (
e.g.
aldehydes, esters, heterocycles, silyl ketene acetals, alcohols) is then discussed in the context of molecular chemistry. Focus has been placed on the activation of substrates finding analogies with monomers (
e.g.
bis-aldehydes, multi-isocyanates, cyclic esters, epoxides,
N
-carboxyanhydrides,
etc.
) and/or initiators (
e.g.
hydroxy- or trimethylsilyl-containing reagents) employed in such "organopolymerisation" reactions utilizing NHCs. A variety of metal-free polymers, including aliphatic polyesters and polyethers, poly(α-peptoid)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way. The last section covers the use of NHCs as structural components of the polymer chain. Indeed, NHC-based photoinitiators, chain transfer agents or functionalizing agents, as well as bifunctional NHC monomer substrates, can also serve for metal-free polymer synthesis.
This review covers the contribution of NHCs in metal-free polymer synthesis, as organocatalysts in polymerization reactions and as structural components of polymer chains. |
doi_str_mv | 10.1039/c2cs35383k |
format | Article |
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N
-heterocyclic carbenes (NHCs) has witnessed tremendous development in the past two decades: NHCs have not only become versatile ligands for transition metals, but have also emerged as powerful organic catalysts in molecular chemistry and, more recently, in metal-free polymer synthesis. To understand the success of NHCs, this review first presents the electronic properties of NHCs, their main synthetic methods, their handling, and their reactivity. Their ability to activate key functional groups (
e.g.
aldehydes, esters, heterocycles, silyl ketene acetals, alcohols) is then discussed in the context of molecular chemistry. Focus has been placed on the activation of substrates finding analogies with monomers (
e.g.
bis-aldehydes, multi-isocyanates, cyclic esters, epoxides,
N
-carboxyanhydrides,
etc.
) and/or initiators (
e.g.
hydroxy- or trimethylsilyl-containing reagents) employed in such "organopolymerisation" reactions utilizing NHCs. A variety of metal-free polymers, including aliphatic polyesters and polyethers, poly(α-peptoid)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way. The last section covers the use of NHCs as structural components of the polymer chain. Indeed, NHC-based photoinitiators, chain transfer agents or functionalizing agents, as well as bifunctional NHC monomer substrates, can also serve for metal-free polymer synthesis.
This review covers the contribution of NHCs in metal-free polymer synthesis, as organocatalysts in polymerization reactions and as structural components of polymer chains.</description><identifier>ISSN: 0306-0012</identifier><identifier>EISSN: 1460-4744</identifier><identifier>DOI: 10.1039/c2cs35383k</identifier><identifier>PMID: 23288304</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Activation ; Carbenes ; Chain transfer ; Chemical Sciences ; Esters ; Monomers ; Polymers ; Polysiloxanes ; Synthesis ; Synthesis (chemistry)</subject><ispartof>Chemical Society reviews, 2013-01, Vol.42 (5), p.2142-2172</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c468t-17150dde6d7a8e015184d3f81682dededb4548ba240bbe9d306c80aaf6eb2dff3</citedby><cites>FETCH-LOGICAL-c468t-17150dde6d7a8e015184d3f81682dededb4548ba240bbe9d306c80aaf6eb2dff3</cites><orcidid>0000-0003-4446-3771</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23288304$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00932343$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Fèvre, Maréva</creatorcontrib><creatorcontrib>Pinaud, Julien</creatorcontrib><creatorcontrib>Gnanou, Yves</creatorcontrib><creatorcontrib>Vignolle, Joan</creatorcontrib><creatorcontrib>Taton, Daniel</creatorcontrib><title>N-Heterocyclic carbenes (NHCs) as organocatalysts and structural components in metal-free polymer synthesis</title><title>Chemical Society reviews</title><addtitle>Chem Soc Rev</addtitle><description>The chemistry of
N
-heterocyclic carbenes (NHCs) has witnessed tremendous development in the past two decades: NHCs have not only become versatile ligands for transition metals, but have also emerged as powerful organic catalysts in molecular chemistry and, more recently, in metal-free polymer synthesis. To understand the success of NHCs, this review first presents the electronic properties of NHCs, their main synthetic methods, their handling, and their reactivity. Their ability to activate key functional groups (
e.g.
aldehydes, esters, heterocycles, silyl ketene acetals, alcohols) is then discussed in the context of molecular chemistry. Focus has been placed on the activation of substrates finding analogies with monomers (
e.g.
bis-aldehydes, multi-isocyanates, cyclic esters, epoxides,
N
-carboxyanhydrides,
etc.
) and/or initiators (
e.g.
hydroxy- or trimethylsilyl-containing reagents) employed in such "organopolymerisation" reactions utilizing NHCs. A variety of metal-free polymers, including aliphatic polyesters and polyethers, poly(α-peptoid)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way. The last section covers the use of NHCs as structural components of the polymer chain. Indeed, NHC-based photoinitiators, chain transfer agents or functionalizing agents, as well as bifunctional NHC monomer substrates, can also serve for metal-free polymer synthesis.
This review covers the contribution of NHCs in metal-free polymer synthesis, as organocatalysts in polymerization reactions and as structural components of polymer chains.</description><subject>Activation</subject><subject>Carbenes</subject><subject>Chain transfer</subject><subject>Chemical Sciences</subject><subject>Esters</subject><subject>Monomers</subject><subject>Polymers</subject><subject>Polysiloxanes</subject><subject>Synthesis</subject><subject>Synthesis (chemistry)</subject><issn>0306-0012</issn><issn>1460-4744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqN0U1v1DAQBmALgehSuHAHmVuLFBh_rOM9VivKIq3KBc6RY09oaBIHT1Ip_x6vtt3eEPLBlufRqxkNY28FfBKgNp-99KTWyqq7Z2wltIFCl1o_ZytQYAoAIc_YK6Lf-SVKI1-yM6mktQr0it3dFDucMEW_-K713LtU44DEL252W7rkjnhMv9wQvZtct9BE3A2B05RmP83JddzHfowDDrnSDrzHzIomIfIxdkuPidMyTLdILb1mLxrXEb55uM_Zz-svP7a7Yv_967ft1b7w2tipEKVYQwhoQuksglgLq4NqrDBWBsyn1mttayc11DVuQh7SW3CuMVjL0DTqnF0ec29dV42p7V1aqujaane1rw5_ABsllVb3ItuLox1T_DMjTVXfkseucwPGmSpRWiPKEsx_UGlLZcFYyPTjkfoUiRI2pzYEVIedVU87y_j9Q-5c9xhO9HFJGXw4gkT-VH0KqMZwmPndv4z6C9ACp_k</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Fèvre, Maréva</creator><creator>Pinaud, Julien</creator><creator>Gnanou, Yves</creator><creator>Vignolle, Joan</creator><creator>Taton, Daniel</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0003-4446-3771</orcidid></search><sort><creationdate>20130101</creationdate><title>N-Heterocyclic carbenes (NHCs) as organocatalysts and structural components in metal-free polymer synthesis</title><author>Fèvre, Maréva ; Pinaud, Julien ; Gnanou, Yves ; Vignolle, Joan ; Taton, Daniel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c468t-17150dde6d7a8e015184d3f81682dededb4548ba240bbe9d306c80aaf6eb2dff3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Activation</topic><topic>Carbenes</topic><topic>Chain transfer</topic><topic>Chemical Sciences</topic><topic>Esters</topic><topic>Monomers</topic><topic>Polymers</topic><topic>Polysiloxanes</topic><topic>Synthesis</topic><topic>Synthesis (chemistry)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fèvre, Maréva</creatorcontrib><creatorcontrib>Pinaud, Julien</creatorcontrib><creatorcontrib>Gnanou, Yves</creatorcontrib><creatorcontrib>Vignolle, Joan</creatorcontrib><creatorcontrib>Taton, Daniel</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Hyper Article en Ligne (HAL)</collection><jtitle>Chemical Society reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fèvre, Maréva</au><au>Pinaud, Julien</au><au>Gnanou, Yves</au><au>Vignolle, Joan</au><au>Taton, Daniel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>N-Heterocyclic carbenes (NHCs) as organocatalysts and structural components in metal-free polymer synthesis</atitle><jtitle>Chemical Society reviews</jtitle><addtitle>Chem Soc Rev</addtitle><date>2013-01-01</date><risdate>2013</risdate><volume>42</volume><issue>5</issue><spage>2142</spage><epage>2172</epage><pages>2142-2172</pages><issn>0306-0012</issn><eissn>1460-4744</eissn><abstract>The chemistry of
N
-heterocyclic carbenes (NHCs) has witnessed tremendous development in the past two decades: NHCs have not only become versatile ligands for transition metals, but have also emerged as powerful organic catalysts in molecular chemistry and, more recently, in metal-free polymer synthesis. To understand the success of NHCs, this review first presents the electronic properties of NHCs, their main synthetic methods, their handling, and their reactivity. Their ability to activate key functional groups (
e.g.
aldehydes, esters, heterocycles, silyl ketene acetals, alcohols) is then discussed in the context of molecular chemistry. Focus has been placed on the activation of substrates finding analogies with monomers (
e.g.
bis-aldehydes, multi-isocyanates, cyclic esters, epoxides,
N
-carboxyanhydrides,
etc.
) and/or initiators (
e.g.
hydroxy- or trimethylsilyl-containing reagents) employed in such "organopolymerisation" reactions utilizing NHCs. A variety of metal-free polymers, including aliphatic polyesters and polyethers, poly(α-peptoid)s, poly(meth)acrylates, polyurethanes, or polysiloxanes can be obtained in this way. The last section covers the use of NHCs as structural components of the polymer chain. Indeed, NHC-based photoinitiators, chain transfer agents or functionalizing agents, as well as bifunctional NHC monomer substrates, can also serve for metal-free polymer synthesis.
This review covers the contribution of NHCs in metal-free polymer synthesis, as organocatalysts in polymerization reactions and as structural components of polymer chains.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>23288304</pmid><doi>10.1039/c2cs35383k</doi><tpages>31</tpages><orcidid>https://orcid.org/0000-0003-4446-3771</orcidid></addata></record> |
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source | Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
subjects | Activation Carbenes Chain transfer Chemical Sciences Esters Monomers Polymers Polysiloxanes Synthesis Synthesis (chemistry) |
title | N-Heterocyclic carbenes (NHCs) as organocatalysts and structural components in metal-free polymer synthesis |
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