Topochemical polymerizations for the solid-state synthesis of organic polymers
Topochemical polymerizations are solid-state reactions driven by the alignment of monomers in the crystalline state. The molecular confinement in the monomer crystal lattice offers precise control over the tacticity, packing and crystallinity of the polymer formed in the topochemical reaction. As to...
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Veröffentlicht in: | Chemical Society reviews 2021-03, Vol.5 (6), p.462-499 |
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description | Topochemical polymerizations are solid-state reactions driven by the alignment of monomers in the crystalline state. The molecular confinement in the monomer crystal lattice offers precise control over the tacticity, packing and crystallinity of the polymer formed in the topochemical reaction. As topochemical reactions occur under solvent- and catalyst-free conditions, giving products in high yield and selectivity/specificity that do not require tedious chromatographic purification, topochemical polymerizations are highly attractive over traditional solution-phase polymer synthesis. By this method, polymers having sophisticated structures and desired topologies can be availed. Often, such ordered packing confers attractive properties to the topochemically-synthesized polymers. Diverse categories of topochemical polymerizations are known, such as polymerizations
via
[2+2], [4+4], [4+2], and [3+2] cycloadditions, and polymerization of diynes, triynes, dienes, trienes, and quinodimethanes, each of which proceed under suitable stimuli like heat, light or pressure. Each class of these reactions requires a unique packing arrangement of the corresponding monomers for the smooth reaction and produces polymers with distinct properties. This review is penned with the intent of bringing all the types of topochemical polymerizations into a single platform and communicating the versatility of these lattice-controlled polymerizations. We present a brief history of the development of each category and comprehensively review the topochemical synthesis of fully-organic polymers reported in the last twenty years, particularly in crystals. We mainly focus on the various molecular designs and crystal engineering strategies adopted to align monomers in a suitable orientation for polymerization. Finally, we analyze the current challenges and future perspectives in this research field.
This review summarizes the different categories of topochemical polymerizations for the synthesis of fully-organic polymers and their design strategies. |
doi_str_mv | 10.1039/d0cs00840k |
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via
[2+2], [4+4], [4+2], and [3+2] cycloadditions, and polymerization of diynes, triynes, dienes, trienes, and quinodimethanes, each of which proceed under suitable stimuli like heat, light or pressure. Each class of these reactions requires a unique packing arrangement of the corresponding monomers for the smooth reaction and produces polymers with distinct properties. This review is penned with the intent of bringing all the types of topochemical polymerizations into a single platform and communicating the versatility of these lattice-controlled polymerizations. We present a brief history of the development of each category and comprehensively review the topochemical synthesis of fully-organic polymers reported in the last twenty years, particularly in crystals. We mainly focus on the various molecular designs and crystal engineering strategies adopted to align monomers in a suitable orientation for polymerization. Finally, we analyze the current challenges and future perspectives in this research field.
This review summarizes the different categories of topochemical polymerizations for the synthesis of fully-organic polymers and their design strategies.</description><identifier>ISSN: 0306-0012</identifier><identifier>EISSN: 1460-4744</identifier><identifier>DOI: 10.1039/d0cs00840k</identifier><identifier>PMID: 33543741</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Chemical synthesis ; Communication ; Crystal lattices ; Crystal structure ; Crystallinity ; Dienes ; Monomers ; Polymerization ; Polymers ; Selectivity ; Solid state ; Tacticity ; Topology ; Trienes</subject><ispartof>Chemical Society reviews, 2021-03, Vol.5 (6), p.462-499</ispartof><rights>Copyright Royal Society of Chemistry 2021</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c444t-fac17dba1bf2ac622ccd39a0e0a2052d19acba27d856c10c2a9bc48eb47f79443</citedby><cites>FETCH-LOGICAL-c444t-fac17dba1bf2ac622ccd39a0e0a2052d19acba27d856c10c2a9bc48eb47f79443</cites><orcidid>0000-0002-4005-3655 ; 0000-0002-8416-9764 ; 0000-0002-6398-5383 ; 0000-0003-3779-5655 ; 0000-0001-5939-9288 ; 0000-0001-9801-7772</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33543741$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hema, Kuntrapakam</creatorcontrib><creatorcontrib>Ravi, Arthi</creatorcontrib><creatorcontrib>Raju, Cijil</creatorcontrib><creatorcontrib>Pathan, Javed R</creatorcontrib><creatorcontrib>Rai, Rishika</creatorcontrib><creatorcontrib>Sureshan, Kana M</creatorcontrib><title>Topochemical polymerizations for the solid-state synthesis of organic polymers</title><title>Chemical Society reviews</title><addtitle>Chem Soc Rev</addtitle><description>Topochemical polymerizations are solid-state reactions driven by the alignment of monomers in the crystalline state. The molecular confinement in the monomer crystal lattice offers precise control over the tacticity, packing and crystallinity of the polymer formed in the topochemical reaction. As topochemical reactions occur under solvent- and catalyst-free conditions, giving products in high yield and selectivity/specificity that do not require tedious chromatographic purification, topochemical polymerizations are highly attractive over traditional solution-phase polymer synthesis. By this method, polymers having sophisticated structures and desired topologies can be availed. Often, such ordered packing confers attractive properties to the topochemically-synthesized polymers. Diverse categories of topochemical polymerizations are known, such as polymerizations
via
[2+2], [4+4], [4+2], and [3+2] cycloadditions, and polymerization of diynes, triynes, dienes, trienes, and quinodimethanes, each of which proceed under suitable stimuli like heat, light or pressure. Each class of these reactions requires a unique packing arrangement of the corresponding monomers for the smooth reaction and produces polymers with distinct properties. This review is penned with the intent of bringing all the types of topochemical polymerizations into a single platform and communicating the versatility of these lattice-controlled polymerizations. We present a brief history of the development of each category and comprehensively review the topochemical synthesis of fully-organic polymers reported in the last twenty years, particularly in crystals. We mainly focus on the various molecular designs and crystal engineering strategies adopted to align monomers in a suitable orientation for polymerization. Finally, we analyze the current challenges and future perspectives in this research field.
This review summarizes the different categories of topochemical polymerizations for the synthesis of fully-organic polymers and their design strategies.</description><subject>Chemical synthesis</subject><subject>Communication</subject><subject>Crystal lattices</subject><subject>Crystal structure</subject><subject>Crystallinity</subject><subject>Dienes</subject><subject>Monomers</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Selectivity</subject><subject>Solid state</subject><subject>Tacticity</subject><subject>Topology</subject><subject>Trienes</subject><issn>0306-0012</issn><issn>1460-4744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpdkUlPwzAQhS0EoqVw4Q6KxAUhBcZLtiMqq6jgQDlHjuNQlyQunuRQfj2GLkic5mnmm6fRG0KOKVxS4NlVCQoBUgEfO2RIRQyhSITYJUPgEIcAlA3IAeLcK5rEbJ8MOI8ETwQdkuepXVg1041Rsg4Wtl422pkv2RnbYlBZF3QzHaCtTRliJzuvl61vocHAVoF177I1arOIh2SvkjXqo3Udkbe72-n4IZy83D-OryehEkJ0YSUVTcpC0qJiUsWMKVXyTIIGySBiJc2kKiRLyjSKFQXFZFYokepCJFWSCcFH5Hzlu3D2s9fY5Y1Bpetattr2mDORJjQCFnOPnv1D57Z3rb8uZxHEEYtSSD11saKUs4hOV_nCmUa6ZU4h_0k5v4Hx62_KTx4-XVv2RaPLLbqJ1QMnK8Ch2k7_3sS_AZh7gkc</recordid><startdate>20210321</startdate><enddate>20210321</enddate><creator>Hema, Kuntrapakam</creator><creator>Ravi, Arthi</creator><creator>Raju, Cijil</creator><creator>Pathan, Javed R</creator><creator>Rai, Rishika</creator><creator>Sureshan, Kana M</creator><general>Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-4005-3655</orcidid><orcidid>https://orcid.org/0000-0002-8416-9764</orcidid><orcidid>https://orcid.org/0000-0002-6398-5383</orcidid><orcidid>https://orcid.org/0000-0003-3779-5655</orcidid><orcidid>https://orcid.org/0000-0001-5939-9288</orcidid><orcidid>https://orcid.org/0000-0001-9801-7772</orcidid></search><sort><creationdate>20210321</creationdate><title>Topochemical polymerizations for the solid-state synthesis of organic polymers</title><author>Hema, Kuntrapakam ; Ravi, Arthi ; Raju, Cijil ; Pathan, Javed R ; Rai, Rishika ; Sureshan, Kana M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c444t-fac17dba1bf2ac622ccd39a0e0a2052d19acba27d856c10c2a9bc48eb47f79443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Chemical synthesis</topic><topic>Communication</topic><topic>Crystal lattices</topic><topic>Crystal structure</topic><topic>Crystallinity</topic><topic>Dienes</topic><topic>Monomers</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Selectivity</topic><topic>Solid state</topic><topic>Tacticity</topic><topic>Topology</topic><topic>Trienes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hema, Kuntrapakam</creatorcontrib><creatorcontrib>Ravi, Arthi</creatorcontrib><creatorcontrib>Raju, Cijil</creatorcontrib><creatorcontrib>Pathan, Javed R</creatorcontrib><creatorcontrib>Rai, Rishika</creatorcontrib><creatorcontrib>Sureshan, Kana M</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Chemical Society reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hema, Kuntrapakam</au><au>Ravi, Arthi</au><au>Raju, Cijil</au><au>Pathan, Javed R</au><au>Rai, Rishika</au><au>Sureshan, Kana M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Topochemical polymerizations for the solid-state synthesis of organic polymers</atitle><jtitle>Chemical Society reviews</jtitle><addtitle>Chem Soc Rev</addtitle><date>2021-03-21</date><risdate>2021</risdate><volume>5</volume><issue>6</issue><spage>462</spage><epage>499</epage><pages>462-499</pages><issn>0306-0012</issn><eissn>1460-4744</eissn><abstract>Topochemical polymerizations are solid-state reactions driven by the alignment of monomers in the crystalline state. The molecular confinement in the monomer crystal lattice offers precise control over the tacticity, packing and crystallinity of the polymer formed in the topochemical reaction. As topochemical reactions occur under solvent- and catalyst-free conditions, giving products in high yield and selectivity/specificity that do not require tedious chromatographic purification, topochemical polymerizations are highly attractive over traditional solution-phase polymer synthesis. By this method, polymers having sophisticated structures and desired topologies can be availed. Often, such ordered packing confers attractive properties to the topochemically-synthesized polymers. Diverse categories of topochemical polymerizations are known, such as polymerizations
via
[2+2], [4+4], [4+2], and [3+2] cycloadditions, and polymerization of diynes, triynes, dienes, trienes, and quinodimethanes, each of which proceed under suitable stimuli like heat, light or pressure. Each class of these reactions requires a unique packing arrangement of the corresponding monomers for the smooth reaction and produces polymers with distinct properties. This review is penned with the intent of bringing all the types of topochemical polymerizations into a single platform and communicating the versatility of these lattice-controlled polymerizations. We present a brief history of the development of each category and comprehensively review the topochemical synthesis of fully-organic polymers reported in the last twenty years, particularly in crystals. We mainly focus on the various molecular designs and crystal engineering strategies adopted to align monomers in a suitable orientation for polymerization. Finally, we analyze the current challenges and future perspectives in this research field.
This review summarizes the different categories of topochemical polymerizations for the synthesis of fully-organic polymers and their design strategies.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>33543741</pmid><doi>10.1039/d0cs00840k</doi><tpages>38</tpages><orcidid>https://orcid.org/0000-0002-4005-3655</orcidid><orcidid>https://orcid.org/0000-0002-8416-9764</orcidid><orcidid>https://orcid.org/0000-0002-6398-5383</orcidid><orcidid>https://orcid.org/0000-0003-3779-5655</orcidid><orcidid>https://orcid.org/0000-0001-5939-9288</orcidid><orcidid>https://orcid.org/0000-0001-9801-7772</orcidid></addata></record> |
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subjects | Chemical synthesis Communication Crystal lattices Crystal structure Crystallinity Dienes Monomers Polymerization Polymers Selectivity Solid state Tacticity Topology Trienes |
title | Topochemical polymerizations for the solid-state synthesis of organic polymers |
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