Synthesis and characterization of new monomeric and polymeric phthalocyanines

Monomeric (M = 2Li or 2H) and polymeric (M = 2H, Zn, Cu, Co, or Ni), where M is metal or hydrogen, phthalocyanines were prepared by the tetramerization reaction of bisphthalonitrile monomer with appropriate materials. The electrical conductivities of the polymeric phthalocyanines, which were measure...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of applied polymer science 2008-11, Vol.110 (4), p.2115-2126
Hauptverfasser: Bilgin, A, Yağcı, Ç, Mendi, A, Yıldız, U
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2126
container_issue 4
container_start_page 2115
container_title Journal of applied polymer science
container_volume 110
creator Bilgin, A
Yağcı, Ç
Mendi, A
Yıldız, U
description Monomeric (M = 2Li or 2H) and polymeric (M = 2H, Zn, Cu, Co, or Ni), where M is metal or hydrogen, phthalocyanines were prepared by the tetramerization reaction of bisphthalonitrile monomer with appropriate materials. The electrical conductivities of the polymeric phthalocyanines, which were measured as gold sandwiches, were found to be 10⁻¹⁰-10⁻⁷ S/cm in vacuo and in air. The binding property of a Co-containing polymeric phthalocyanine (10) toward alkali, alkaline-earth, and some heavy cations was studied in tetrahydrofuran. The extraction affinity of 10 for K⁺ was found to be the highest in the heterogeneous phase extraction experiments. The disaggregation property of a Ni-containing polymeric phthalocyanine (11) was investigated with K⁺, Na⁺, and NH₄⁺ cations. The intrinsic viscosities of all polymers were also measured by means of viscometry. All the novel compounds were characterized with elemental analysis, ultraviolet-visible, Fourier transform infrared, NMR, and mass spectrometry spectral data, and differential thermal analysis/thermogravimetry.
doi_str_mv 10.1002/app.28774
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_35204174</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>35204174</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4584-ff041cc1d8711e352bc0c4a54342c0f14ca969b26891b56d18deda843c353cc03</originalsourceid><addsrcrecordid>eNp1kM1u1TAQRiMEEpfCgicgG5BYpB3_xllWFRRQgYpSdWnNnThcQ64d7FQlPD2mKd2xssZzvmPrq6rnDA4ZAD_CaTrkpm3lg2rDoGsbqbl5WG3KjjWm69Tj6knO3wEYU6A31ceLJcw7l32uMfQ17TAhzS753zj7GOo41MHd1PsY4r7c0i01xXFZp2k373CMtGDwweWn1aMBx-ye3Z0H1eXbN19P3jVnn0_fnxyfNSSVkc0wgGRErDctY04oviUgiUoKyQkGJgk73W25Nh3bKt0z07sejRQklCACcVC9Wr1Tij-vXZ7t3mdy44jBxetsi7K80MoCvl5BSjHn5AY7Jb_HtFgG9m9hthRmbwsr7Ms7KWbCcUgYyOf7AAcDynBVuKOVu_GjW_4vtMfn5__MzZrweXa_7hOYfljdilbZq0-n9gMXV5qLL1YX_sXKDxgtfkvlF5cXHJgApoQGBeIPDjaSYg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>35204174</pqid></control><display><type>article</type><title>Synthesis and characterization of new monomeric and polymeric phthalocyanines</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Bilgin, A ; Yağcı, Ç ; Mendi, A ; Yıldız, U</creator><creatorcontrib>Bilgin, A ; Yağcı, Ç ; Mendi, A ; Yıldız, U</creatorcontrib><description>Monomeric (M = 2Li or 2H) and polymeric (M = 2H, Zn, Cu, Co, or Ni), where M is metal or hydrogen, phthalocyanines were prepared by the tetramerization reaction of bisphthalonitrile monomer with appropriate materials. The electrical conductivities of the polymeric phthalocyanines, which were measured as gold sandwiches, were found to be 10⁻¹⁰-10⁻⁷ S/cm in vacuo and in air. The binding property of a Co-containing polymeric phthalocyanine (10) toward alkali, alkaline-earth, and some heavy cations was studied in tetrahydrofuran. The extraction affinity of 10 for K⁺ was found to be the highest in the heterogeneous phase extraction experiments. The disaggregation property of a Ni-containing polymeric phthalocyanine (11) was investigated with K⁺, Na⁺, and NH₄⁺ cations. The intrinsic viscosities of all polymers were also measured by means of viscometry. All the novel compounds were characterized with elemental analysis, ultraviolet-visible, Fourier transform infrared, NMR, and mass spectrometry spectral data, and differential thermal analysis/thermogravimetry.</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.28774</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; conducting polymers ; dyes/pigments ; Exact sciences and technology ; Inorganic and organomineral polymers ; macrocycles ; Physicochemistry of polymers ; polyphthalocyanines ; Preparation</subject><ispartof>Journal of applied polymer science, 2008-11, Vol.110 (4), p.2115-2126</ispartof><rights>Copyright © 2008 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4584-ff041cc1d8711e352bc0c4a54342c0f14ca969b26891b56d18deda843c353cc03</citedby><cites>FETCH-LOGICAL-c4584-ff041cc1d8711e352bc0c4a54342c0f14ca969b26891b56d18deda843c353cc03</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%2Fapp.28774$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.28774$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27922,27923,45572,45573</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=20805825$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Bilgin, A</creatorcontrib><creatorcontrib>Yağcı, Ç</creatorcontrib><creatorcontrib>Mendi, A</creatorcontrib><creatorcontrib>Yıldız, U</creatorcontrib><title>Synthesis and characterization of new monomeric and polymeric phthalocyanines</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>Monomeric (M = 2Li or 2H) and polymeric (M = 2H, Zn, Cu, Co, or Ni), where M is metal or hydrogen, phthalocyanines were prepared by the tetramerization reaction of bisphthalonitrile monomer with appropriate materials. The electrical conductivities of the polymeric phthalocyanines, which were measured as gold sandwiches, were found to be 10⁻¹⁰-10⁻⁷ S/cm in vacuo and in air. The binding property of a Co-containing polymeric phthalocyanine (10) toward alkali, alkaline-earth, and some heavy cations was studied in tetrahydrofuran. The extraction affinity of 10 for K⁺ was found to be the highest in the heterogeneous phase extraction experiments. The disaggregation property of a Ni-containing polymeric phthalocyanine (11) was investigated with K⁺, Na⁺, and NH₄⁺ cations. The intrinsic viscosities of all polymers were also measured by means of viscometry. All the novel compounds were characterized with elemental analysis, ultraviolet-visible, Fourier transform infrared, NMR, and mass spectrometry spectral data, and differential thermal analysis/thermogravimetry.</description><subject>Applied sciences</subject><subject>conducting polymers</subject><subject>dyes/pigments</subject><subject>Exact sciences and technology</subject><subject>Inorganic and organomineral polymers</subject><subject>macrocycles</subject><subject>Physicochemistry of polymers</subject><subject>polyphthalocyanines</subject><subject>Preparation</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNp1kM1u1TAQRiMEEpfCgicgG5BYpB3_xllWFRRQgYpSdWnNnThcQ64d7FQlPD2mKd2xssZzvmPrq6rnDA4ZAD_CaTrkpm3lg2rDoGsbqbl5WG3KjjWm69Tj6knO3wEYU6A31ceLJcw7l32uMfQ17TAhzS753zj7GOo41MHd1PsY4r7c0i01xXFZp2k373CMtGDwweWn1aMBx-ye3Z0H1eXbN19P3jVnn0_fnxyfNSSVkc0wgGRErDctY04oviUgiUoKyQkGJgk73W25Nh3bKt0z07sejRQklCACcVC9Wr1Tij-vXZ7t3mdy44jBxetsi7K80MoCvl5BSjHn5AY7Jb_HtFgG9m9hthRmbwsr7Ms7KWbCcUgYyOf7AAcDynBVuKOVu_GjW_4vtMfn5__MzZrweXa_7hOYfljdilbZq0-n9gMXV5qLL1YX_sXKDxgtfkvlF5cXHJgApoQGBeIPDjaSYg</recordid><startdate>20081115</startdate><enddate>20081115</enddate><creator>Bilgin, A</creator><creator>Yağcı, Ç</creator><creator>Mendi, A</creator><creator>Yıldız, U</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20081115</creationdate><title>Synthesis and characterization of new monomeric and polymeric phthalocyanines</title><author>Bilgin, A ; Yağcı, Ç ; Mendi, A ; Yıldız, U</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4584-ff041cc1d8711e352bc0c4a54342c0f14ca969b26891b56d18deda843c353cc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Applied sciences</topic><topic>conducting polymers</topic><topic>dyes/pigments</topic><topic>Exact sciences and technology</topic><topic>Inorganic and organomineral polymers</topic><topic>macrocycles</topic><topic>Physicochemistry of polymers</topic><topic>polyphthalocyanines</topic><topic>Preparation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bilgin, A</creatorcontrib><creatorcontrib>Yağcı, Ç</creatorcontrib><creatorcontrib>Mendi, A</creatorcontrib><creatorcontrib>Yıldız, U</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bilgin, A</au><au>Yağcı, Ç</au><au>Mendi, A</au><au>Yıldız, U</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and characterization of new monomeric and polymeric phthalocyanines</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2008-11-15</date><risdate>2008</risdate><volume>110</volume><issue>4</issue><spage>2115</spage><epage>2126</epage><pages>2115-2126</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>Monomeric (M = 2Li or 2H) and polymeric (M = 2H, Zn, Cu, Co, or Ni), where M is metal or hydrogen, phthalocyanines were prepared by the tetramerization reaction of bisphthalonitrile monomer with appropriate materials. The electrical conductivities of the polymeric phthalocyanines, which were measured as gold sandwiches, were found to be 10⁻¹⁰-10⁻⁷ S/cm in vacuo and in air. The binding property of a Co-containing polymeric phthalocyanine (10) toward alkali, alkaline-earth, and some heavy cations was studied in tetrahydrofuran. The extraction affinity of 10 for K⁺ was found to be the highest in the heterogeneous phase extraction experiments. The disaggregation property of a Ni-containing polymeric phthalocyanine (11) was investigated with K⁺, Na⁺, and NH₄⁺ cations. The intrinsic viscosities of all polymers were also measured by means of viscometry. All the novel compounds were characterized with elemental analysis, ultraviolet-visible, Fourier transform infrared, NMR, and mass spectrometry spectral data, and differential thermal analysis/thermogravimetry.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/app.28774</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0021-8995
ispartof Journal of applied polymer science, 2008-11, Vol.110 (4), p.2115-2126
issn 0021-8995
1097-4628
language eng
recordid cdi_proquest_miscellaneous_35204174
source Wiley Online Library Journals Frontfile Complete
subjects Applied sciences
conducting polymers
dyes/pigments
Exact sciences and technology
Inorganic and organomineral polymers
macrocycles
Physicochemistry of polymers
polyphthalocyanines
Preparation
title Synthesis and characterization of new monomeric and polymeric phthalocyanines
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-10T04%3A59%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20characterization%20of%20new%20monomeric%20and%20polymeric%20phthalocyanines&rft.jtitle=Journal%20of%20applied%20polymer%20science&rft.au=Bilgin,%20A&rft.date=2008-11-15&rft.volume=110&rft.issue=4&rft.spage=2115&rft.epage=2126&rft.pages=2115-2126&rft.issn=0021-8995&rft.eissn=1097-4628&rft.coden=JAPNAB&rft_id=info:doi/10.1002/app.28774&rft_dat=%3Cproquest_cross%3E35204174%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=35204174&rft_id=info:pmid/&rfr_iscdi=true