Polyaddition of vinyl ethers and phthalaldehydes successive cyclotrimerization reactions: selective model reactions and synthesis of acid-degradable linear poly(cyclic acetal)s
A polyaddition reaction via the cyclotrimerization of one vinyl ether and two conjugated dialdehyde molecules successfully proceeded using EtAlCl 2 as a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain. The use of a low-reactive or non-polymerizable vinyl ether...
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Veröffentlicht in: | Polymer chemistry 2019-03, Vol.1 (11), p.1377-1385 |
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creator | Naito, Tadashi Kanazawa, Arihiro Aoshima, Sadahito |
description | A polyaddition reaction
via
the cyclotrimerization of one vinyl ether and two conjugated dialdehyde molecules successfully proceeded using EtAlCl
2
as a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain. The use of a low-reactive or non-polymerizable vinyl ether and the choice of adequate catalysts were extremely important for the effective cyclotrimerization reactions. Diphenylethylene was also efficiently polymerized with dialdehydes. The polymers obtained by the polyaddition reaction showed selective acid-degradability and high glass-transition temperatures based on the cyclic acetal structures in the main chain.
A polyaddition
via
the cyclotrimerization of one vinyl monomer and two conjugated dialdehydes proceeded using a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain. |
doi_str_mv | 10.1039/c9py00043g |
format | Article |
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via
the cyclotrimerization of one vinyl ether and two conjugated dialdehyde molecules successfully proceeded using EtAlCl
2
as a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain. The use of a low-reactive or non-polymerizable vinyl ether and the choice of adequate catalysts were extremely important for the effective cyclotrimerization reactions. Diphenylethylene was also efficiently polymerized with dialdehydes. The polymers obtained by the polyaddition reaction showed selective acid-degradability and high glass-transition temperatures based on the cyclic acetal structures in the main chain.
A polyaddition
via
the cyclotrimerization of one vinyl monomer and two conjugated dialdehydes proceeded using a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain.</description><identifier>ISSN: 1759-9954</identifier><identifier>EISSN: 1759-9962</identifier><identifier>DOI: 10.1039/c9py00043g</identifier><ispartof>Polymer chemistry, 2019-03, Vol.1 (11), p.1377-1385</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Naito, Tadashi</creatorcontrib><creatorcontrib>Kanazawa, Arihiro</creatorcontrib><creatorcontrib>Aoshima, Sadahito</creatorcontrib><title>Polyaddition of vinyl ethers and phthalaldehydes successive cyclotrimerization reactions: selective model reactions and synthesis of acid-degradable linear poly(cyclic acetal)s</title><title>Polymer chemistry</title><description>A polyaddition reaction
via
the cyclotrimerization of one vinyl ether and two conjugated dialdehyde molecules successfully proceeded using EtAlCl
2
as a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain. The use of a low-reactive or non-polymerizable vinyl ether and the choice of adequate catalysts were extremely important for the effective cyclotrimerization reactions. Diphenylethylene was also efficiently polymerized with dialdehydes. The polymers obtained by the polyaddition reaction showed selective acid-degradability and high glass-transition temperatures based on the cyclic acetal structures in the main chain.
A polyaddition
via
the cyclotrimerization of one vinyl monomer and two conjugated dialdehydes proceeded using a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain.</description><issn>1759-9954</issn><issn>1759-9962</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkEFLAzEQhYNYsGgv3oUc9bCabbaVeBXFYw_eyzSZdiPTZMnEQvxV_kSzRezR03zwHu89RojrVt23SpsHa4ailOr07kxM28eFaYxZzs__eNFdiBnzR_Uo3XZzvZyK71WkAs757GOQcSsPPhSSmHtMLCE4OfS5BwJy2BeHLPnTWmT2B5S2WIo5-T0m_wXHhIRgR-AnyUhYufr20SGdpGMsl1A72PNYCta7xuEugYMNoSQfEJIc6rbbscTbasEMdMdXYrIFYpz93ktx8_ry_vzWJLbroW6BVNanT-j_9B8MY2eb</recordid><startdate>20190312</startdate><enddate>20190312</enddate><creator>Naito, Tadashi</creator><creator>Kanazawa, Arihiro</creator><creator>Aoshima, Sadahito</creator><scope/></search><sort><creationdate>20190312</creationdate><title>Polyaddition of vinyl ethers and phthalaldehydes successive cyclotrimerization reactions: selective model reactions and synthesis of acid-degradable linear poly(cyclic acetal)s</title><author>Naito, Tadashi ; Kanazawa, Arihiro ; Aoshima, Sadahito</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c9py00043g3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Naito, Tadashi</creatorcontrib><creatorcontrib>Kanazawa, Arihiro</creatorcontrib><creatorcontrib>Aoshima, Sadahito</creatorcontrib><jtitle>Polymer chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Naito, Tadashi</au><au>Kanazawa, Arihiro</au><au>Aoshima, Sadahito</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polyaddition of vinyl ethers and phthalaldehydes successive cyclotrimerization reactions: selective model reactions and synthesis of acid-degradable linear poly(cyclic acetal)s</atitle><jtitle>Polymer chemistry</jtitle><date>2019-03-12</date><risdate>2019</risdate><volume>1</volume><issue>11</issue><spage>1377</spage><epage>1385</epage><pages>1377-1385</pages><issn>1759-9954</issn><eissn>1759-9962</eissn><abstract>A polyaddition reaction
via
the cyclotrimerization of one vinyl ether and two conjugated dialdehyde molecules successfully proceeded using EtAlCl
2
as a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain. The use of a low-reactive or non-polymerizable vinyl ether and the choice of adequate catalysts were extremely important for the effective cyclotrimerization reactions. Diphenylethylene was also efficiently polymerized with dialdehydes. The polymers obtained by the polyaddition reaction showed selective acid-degradability and high glass-transition temperatures based on the cyclic acetal structures in the main chain.
A polyaddition
via
the cyclotrimerization of one vinyl monomer and two conjugated dialdehydes proceeded using a Lewis acid catalyst, yielding a polymer with cyclic acetal structures in the main chain.</abstract><doi>10.1039/c9py00043g</doi><tpages>9</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008- |
title | Polyaddition of vinyl ethers and phthalaldehydes successive cyclotrimerization reactions: selective model reactions and synthesis of acid-degradable linear poly(cyclic acetal)s |
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