Synthesis of poly(sulfonium cation) as an alkylating reagent
Methyl 4‐phenylthiophenyl sulfoxide is polymerized to poly(methyl‐4‐phenylthiophenylsulfonium) in poly(phosphoric acid) with a yield higher than 90%. The demethylation of poly(sufonium cation) is examined to control the composition ratio of the thiophenylene unit in the polycation. The polycation is...
Gespeichert in:
Veröffentlicht in: | Polymers for advanced technologies 1994-09, Vol.5 (9), p.507-512 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 512 |
---|---|
container_issue | 9 |
container_start_page | 507 |
container_title | Polymers for advanced technologies |
container_volume | 5 |
creator | Shouji, E. Nishimura, S. Yamamoto, K. Tsuchida, E. |
description | Methyl 4‐phenylthiophenyl sulfoxide is polymerized to poly(methyl‐4‐phenylthiophenylsulfonium) in poly(phosphoric acid) with a yield higher than 90%. The demethylation of poly(sufonium cation) is examined to control the composition ratio of the thiophenylene unit in the polycation. The polycation is soluble in common solvents due to the alternative structure of phenylene sufide and phenylenesulfonium cation and is easily converted to poly(phenylene sulfide) through the demethylation with a nucleophile. The poly(sulfonium cation) can be applicable as an alkylating agent for phenol, aniline and benzoic acid to the corresponding to anisole, N‐methyl aniline, N,N‐dimethyl aniline and benzoic methyl ester, respectively, with high conversion through the demethylation. These products can be isolated without a complicated purification because poly(phenylene sulfide) is precipitated in the mixture as the side product due to the poor solvent solubility. |
doi_str_mv | 10.1002/pat.1994.220050907 |
format | Article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_pat_1994_220050907</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>PAT220050907</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4027-5406fbfa8346ae859620a1075c205efcb25aa9b9cb8c0fdfdd64e06dc2c39c9a3</originalsourceid><addsrcrecordid>eNqNz0FLwzAUwPEgCs7pF_CUox46X9KmaWCXOXUKQ8VNdgyvaTLrunY0Hdpvb8dkePSURx6_B39CLhkMGAC_2WAzYEpFA84BBCiQR6THQKmAiYQd7-aIB5JF8pScef8J0O2U7JHhrC2bD-tzTytHN1XRXvlt4aoy366pwSavymuKnmJJsVi1RfdTLmltcWnL5pycOCy8vfh9--T94X4-fgymL5On8WgamAi4DEQEsUsdJmEUo02EijkgAykMB2GdSblAVKkyaWLAZS7L4shCnBluQmUUhn3C93dNXXlfW6c3db7GutUM9K5fd_16168P_R0a7tFXXtj2H0K_juZ_ebDnuW_s94FjvdKxDKXQi-eJvlvcwiyRc_0W_gC6I3AD</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis of poly(sulfonium cation) as an alkylating reagent</title><source>Wiley Online Library All Journals</source><creator>Shouji, E. ; Nishimura, S. ; Yamamoto, K. ; Tsuchida, E.</creator><creatorcontrib>Shouji, E. ; Nishimura, S. ; Yamamoto, K. ; Tsuchida, E.</creatorcontrib><description>Methyl 4‐phenylthiophenyl sulfoxide is polymerized to poly(methyl‐4‐phenylthiophenylsulfonium) in poly(phosphoric acid) with a yield higher than 90%. The demethylation of poly(sufonium cation) is examined to control the composition ratio of the thiophenylene unit in the polycation. The polycation is soluble in common solvents due to the alternative structure of phenylene sufide and phenylenesulfonium cation and is easily converted to poly(phenylene sulfide) through the demethylation with a nucleophile. The poly(sulfonium cation) can be applicable as an alkylating agent for phenol, aniline and benzoic acid to the corresponding to anisole, N‐methyl aniline, N,N‐dimethyl aniline and benzoic methyl ester, respectively, with high conversion through the demethylation. These products can be isolated without a complicated purification because poly(phenylene sulfide) is precipitated in the mixture as the side product due to the poor solvent solubility.</description><identifier>ISSN: 1042-7147</identifier><identifier>EISSN: 1099-1581</identifier><identifier>DOI: 10.1002/pat.1994.220050907</identifier><language>eng</language><publisher>Chichester, UK: John Wiley & Sons, Ltd</publisher><subject>Alkylating reagent ; Demethylation ; Poly(phenylene sulfide) ; Poly(sulfonium cation)</subject><ispartof>Polymers for advanced technologies, 1994-09, Vol.5 (9), p.507-512</ispartof><rights>Copyright © 1994 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4027-5406fbfa8346ae859620a1075c205efcb25aa9b9cb8c0fdfdd64e06dc2c39c9a3</citedby><cites>FETCH-LOGICAL-c4027-5406fbfa8346ae859620a1075c205efcb25aa9b9cb8c0fdfdd64e06dc2c39c9a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fpat.1994.220050907$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpat.1994.220050907$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Shouji, E.</creatorcontrib><creatorcontrib>Nishimura, S.</creatorcontrib><creatorcontrib>Yamamoto, K.</creatorcontrib><creatorcontrib>Tsuchida, E.</creatorcontrib><title>Synthesis of poly(sulfonium cation) as an alkylating reagent</title><title>Polymers for advanced technologies</title><addtitle>Polym. Adv. Technol</addtitle><description>Methyl 4‐phenylthiophenyl sulfoxide is polymerized to poly(methyl‐4‐phenylthiophenylsulfonium) in poly(phosphoric acid) with a yield higher than 90%. The demethylation of poly(sufonium cation) is examined to control the composition ratio of the thiophenylene unit in the polycation. The polycation is soluble in common solvents due to the alternative structure of phenylene sufide and phenylenesulfonium cation and is easily converted to poly(phenylene sulfide) through the demethylation with a nucleophile. The poly(sulfonium cation) can be applicable as an alkylating agent for phenol, aniline and benzoic acid to the corresponding to anisole, N‐methyl aniline, N,N‐dimethyl aniline and benzoic methyl ester, respectively, with high conversion through the demethylation. These products can be isolated without a complicated purification because poly(phenylene sulfide) is precipitated in the mixture as the side product due to the poor solvent solubility.</description><subject>Alkylating reagent</subject><subject>Demethylation</subject><subject>Poly(phenylene sulfide)</subject><subject>Poly(sulfonium cation)</subject><issn>1042-7147</issn><issn>1099-1581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><recordid>eNqNz0FLwzAUwPEgCs7pF_CUox46X9KmaWCXOXUKQ8VNdgyvaTLrunY0Hdpvb8dkePSURx6_B39CLhkMGAC_2WAzYEpFA84BBCiQR6THQKmAiYQd7-aIB5JF8pScef8J0O2U7JHhrC2bD-tzTytHN1XRXvlt4aoy366pwSavymuKnmJJsVi1RfdTLmltcWnL5pycOCy8vfh9--T94X4-fgymL5On8WgamAi4DEQEsUsdJmEUo02EijkgAykMB2GdSblAVKkyaWLAZS7L4shCnBluQmUUhn3C93dNXXlfW6c3db7GutUM9K5fd_16168P_R0a7tFXXtj2H0K_juZ_ebDnuW_s94FjvdKxDKXQi-eJvlvcwiyRc_0W_gC6I3AD</recordid><startdate>199409</startdate><enddate>199409</enddate><creator>Shouji, E.</creator><creator>Nishimura, S.</creator><creator>Yamamoto, K.</creator><creator>Tsuchida, E.</creator><general>John Wiley & Sons, Ltd</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>199409</creationdate><title>Synthesis of poly(sulfonium cation) as an alkylating reagent</title><author>Shouji, E. ; Nishimura, S. ; Yamamoto, K. ; Tsuchida, E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4027-5406fbfa8346ae859620a1075c205efcb25aa9b9cb8c0fdfdd64e06dc2c39c9a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Alkylating reagent</topic><topic>Demethylation</topic><topic>Poly(phenylene sulfide)</topic><topic>Poly(sulfonium cation)</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shouji, E.</creatorcontrib><creatorcontrib>Nishimura, S.</creatorcontrib><creatorcontrib>Yamamoto, K.</creatorcontrib><creatorcontrib>Tsuchida, E.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Polymers for advanced technologies</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shouji, E.</au><au>Nishimura, S.</au><au>Yamamoto, K.</au><au>Tsuchida, E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of poly(sulfonium cation) as an alkylating reagent</atitle><jtitle>Polymers for advanced technologies</jtitle><addtitle>Polym. Adv. Technol</addtitle><date>1994-09</date><risdate>1994</risdate><volume>5</volume><issue>9</issue><spage>507</spage><epage>512</epage><pages>507-512</pages><issn>1042-7147</issn><eissn>1099-1581</eissn><abstract>Methyl 4‐phenylthiophenyl sulfoxide is polymerized to poly(methyl‐4‐phenylthiophenylsulfonium) in poly(phosphoric acid) with a yield higher than 90%. The demethylation of poly(sufonium cation) is examined to control the composition ratio of the thiophenylene unit in the polycation. The polycation is soluble in common solvents due to the alternative structure of phenylene sufide and phenylenesulfonium cation and is easily converted to poly(phenylene sulfide) through the demethylation with a nucleophile. The poly(sulfonium cation) can be applicable as an alkylating agent for phenol, aniline and benzoic acid to the corresponding to anisole, N‐methyl aniline, N,N‐dimethyl aniline and benzoic methyl ester, respectively, with high conversion through the demethylation. These products can be isolated without a complicated purification because poly(phenylene sulfide) is precipitated in the mixture as the side product due to the poor solvent solubility.</abstract><cop>Chichester, UK</cop><pub>John Wiley & Sons, Ltd</pub><doi>10.1002/pat.1994.220050907</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1042-7147 |
ispartof | Polymers for advanced technologies, 1994-09, Vol.5 (9), p.507-512 |
issn | 1042-7147 1099-1581 |
language | eng |
recordid | cdi_crossref_primary_10_1002_pat_1994_220050907 |
source | Wiley Online Library All Journals |
subjects | Alkylating reagent Demethylation Poly(phenylene sulfide) Poly(sulfonium cation) |
title | Synthesis of poly(sulfonium cation) as an alkylating reagent |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T17%3A09%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20poly(sulfonium%20cation)%20as%20an%20alkylating%20reagent&rft.jtitle=Polymers%20for%20advanced%20technologies&rft.au=Shouji,%20E.&rft.date=1994-09&rft.volume=5&rft.issue=9&rft.spage=507&rft.epage=512&rft.pages=507-512&rft.issn=1042-7147&rft.eissn=1099-1581&rft_id=info:doi/10.1002/pat.1994.220050907&rft_dat=%3Cwiley_cross%3EPAT220050907%3C/wiley_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true |