author_facet Bizzarri, P. Costa
Casa, C. Della
Fiorini, M.
Porzio, W.
Bizzarri, P. Costa
Casa, C. Della
Fiorini, M.
Porzio, W.
author Bizzarri, P. Costa
Casa, C. Della
Fiorini, M.
Porzio, W.
spellingShingle Bizzarri, P. Costa
Casa, C. Della
Fiorini, M.
Porzio, W.
Journal of Polymer Science Part A: Polymer Chemistry
Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
Materials Chemistry
Organic Chemistry
Polymers and Plastics
author_sort bizzarri, p. costa
spelling Bizzarri, P. Costa Casa, C. Della Fiorini, M. Porzio, W. 0887-624X 1099-0518 Wiley Materials Chemistry Organic Chemistry Polymers and Plastics http://dx.doi.org/10.1002/pola.1988.080260125 <jats:title>Abstract</jats:title><jats:p>Oligomers containing thianthrene units in the chain are synthesized by AlCl<jats:sub>3</jats:sub>‐catalyzed reaction of diphenylsulfide, thianthrene, poly(<jats:italic>p</jats:italic>‐phenylene sulfide), and poly(<jats:italic>m</jats:italic>‐phenylene disulfide) with sulfur at 80°C. The products are compared with that obtained by the reaction of diphenylsulfide with AlCl<jats:sub>3</jats:sub> at 225°C. IR spectra and elemental analyses are consistent with cyclic chain structures and show a higher cyclization for CHCl<jats:sub>3</jats:sub>‐insoluble fractions. X‐ray diffraction analysis indicates the same structure for the samples obtained with the different methods of synthesis. A possible structural model is tentatively proposed.</jats:p> Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type Journal of Polymer Science Part A: Polymer Chemistry
doi_str_mv 10.1002/pola.1988.080260125
facet_avail Online
finc_class_facet Chemie und Pharmazie
format ElectronicArticle
fullrecord blob:ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9wb2xhLjE5ODguMDgwMjYwMTI1
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9wb2xhLjE5ODguMDgwMjYwMTI1
institution DE-15
DE-Pl11
DE-Rs1
DE-105
DE-14
DE-Ch1
DE-L229
DE-D275
DE-Bn3
DE-Brt1
DE-D161
DE-Gla1
DE-Zi4
imprint Wiley, 1988
imprint_str_mv Wiley, 1988
issn 0887-624X
1099-0518
issn_str_mv 0887-624X
1099-0518
language English
mega_collection Wiley (CrossRef)
match_str bizzarri1988synthesisofintramolecularlycyclizedpolyphenylenesulfidesofthethianthrenetype
publishDateSort 1988
publisher Wiley
recordtype ai
record_format ai
series Journal of Polymer Science Part A: Polymer Chemistry
source_id 49
title Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_unstemmed Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_full Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_fullStr Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_full_unstemmed Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_short Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_sort synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
topic Materials Chemistry
Organic Chemistry
Polymers and Plastics
url http://dx.doi.org/10.1002/pola.1988.080260125
publishDate 1988
physical 255-265
description <jats:title>Abstract</jats:title><jats:p>Oligomers containing thianthrene units in the chain are synthesized by AlCl<jats:sub>3</jats:sub>‐catalyzed reaction of diphenylsulfide, thianthrene, poly(<jats:italic>p</jats:italic>‐phenylene sulfide), and poly(<jats:italic>m</jats:italic>‐phenylene disulfide) with sulfur at 80°C. The products are compared with that obtained by the reaction of diphenylsulfide with AlCl<jats:sub>3</jats:sub> at 225°C. IR spectra and elemental analyses are consistent with cyclic chain structures and show a higher cyclization for CHCl<jats:sub>3</jats:sub>‐insoluble fractions. X‐ray diffraction analysis indicates the same structure for the samples obtained with the different methods of synthesis. A possible structural model is tentatively proposed.</jats:p>
container_issue 1
container_start_page 255
container_title Journal of Polymer Science Part A: Polymer Chemistry
container_volume 26
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
_version_ 1792337202461540354
geogr_code not assigned
last_indexed 2024-03-01T15:12:35.554Z
geogr_code_person not assigned
openURL url_ver=Z39.88-2004&ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fvufind.svn.sourceforge.net%3Agenerator&rft.title=Synthesis+of+intramolecularly+cyclized+poly%28phenylene+sulfide%29s+of+the+thianthrene%E2%80%90type&rft.date=1988-01-01&genre=article&issn=1099-0518&volume=26&issue=1&spage=255&epage=265&pages=255-265&jtitle=Journal+of+Polymer+Science+Part+A%3A+Polymer+Chemistry&atitle=Synthesis+of+intramolecularly+cyclized+poly%28phenylene+sulfide%29s+of+the+thianthrene%E2%80%90type&aulast=Porzio&aufirst=W.&rft_id=info%3Adoi%2F10.1002%2Fpola.1988.080260125&rft.language%5B0%5D=eng
SOLR
_version_ 1792337202461540354
author Bizzarri, P. Costa, Casa, C. Della, Fiorini, M., Porzio, W.
author_facet Bizzarri, P. Costa, Casa, C. Della, Fiorini, M., Porzio, W., Bizzarri, P. Costa, Casa, C. Della, Fiorini, M., Porzio, W.
author_sort bizzarri, p. costa
container_issue 1
container_start_page 255
container_title Journal of Polymer Science Part A: Polymer Chemistry
container_volume 26
description <jats:title>Abstract</jats:title><jats:p>Oligomers containing thianthrene units in the chain are synthesized by AlCl<jats:sub>3</jats:sub>‐catalyzed reaction of diphenylsulfide, thianthrene, poly(<jats:italic>p</jats:italic>‐phenylene sulfide), and poly(<jats:italic>m</jats:italic>‐phenylene disulfide) with sulfur at 80°C. The products are compared with that obtained by the reaction of diphenylsulfide with AlCl<jats:sub>3</jats:sub> at 225°C. IR spectra and elemental analyses are consistent with cyclic chain structures and show a higher cyclization for CHCl<jats:sub>3</jats:sub>‐insoluble fractions. X‐ray diffraction analysis indicates the same structure for the samples obtained with the different methods of synthesis. A possible structural model is tentatively proposed.</jats:p>
doi_str_mv 10.1002/pola.1988.080260125
facet_avail Online
finc_class_facet Chemie und Pharmazie
format ElectronicArticle
format_de105 Article, E-Article
format_de14 Article, E-Article
format_de15 Article, E-Article
format_de520 Article, E-Article
format_de540 Article, E-Article
format_dech1 Article, E-Article
format_ded117 Article, E-Article
format_degla1 E-Article
format_del152 Buch
format_del189 Article, E-Article
format_dezi4 Article
format_dezwi2 Article, E-Article
format_finc Article, E-Article
format_nrw Article, E-Article
geogr_code not assigned
geogr_code_person not assigned
id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9wb2xhLjE5ODguMDgwMjYwMTI1
imprint Wiley, 1988
imprint_str_mv Wiley, 1988
institution DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3, DE-Brt1, DE-D161, DE-Gla1, DE-Zi4
issn 0887-624X, 1099-0518
issn_str_mv 0887-624X, 1099-0518
language English
last_indexed 2024-03-01T15:12:35.554Z
match_str bizzarri1988synthesisofintramolecularlycyclizedpolyphenylenesulfidesofthethianthrenetype
mega_collection Wiley (CrossRef)
physical 255-265
publishDate 1988
publishDateSort 1988
publisher Wiley
record_format ai
recordtype ai
series Journal of Polymer Science Part A: Polymer Chemistry
source_id 49
spelling Bizzarri, P. Costa Casa, C. Della Fiorini, M. Porzio, W. 0887-624X 1099-0518 Wiley Materials Chemistry Organic Chemistry Polymers and Plastics http://dx.doi.org/10.1002/pola.1988.080260125 <jats:title>Abstract</jats:title><jats:p>Oligomers containing thianthrene units in the chain are synthesized by AlCl<jats:sub>3</jats:sub>‐catalyzed reaction of diphenylsulfide, thianthrene, poly(<jats:italic>p</jats:italic>‐phenylene sulfide), and poly(<jats:italic>m</jats:italic>‐phenylene disulfide) with sulfur at 80°C. The products are compared with that obtained by the reaction of diphenylsulfide with AlCl<jats:sub>3</jats:sub> at 225°C. IR spectra and elemental analyses are consistent with cyclic chain structures and show a higher cyclization for CHCl<jats:sub>3</jats:sub>‐insoluble fractions. X‐ray diffraction analysis indicates the same structure for the samples obtained with the different methods of synthesis. A possible structural model is tentatively proposed.</jats:p> Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type Journal of Polymer Science Part A: Polymer Chemistry
spellingShingle Bizzarri, P. Costa, Casa, C. Della, Fiorini, M., Porzio, W., Journal of Polymer Science Part A: Polymer Chemistry, Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type, Materials Chemistry, Organic Chemistry, Polymers and Plastics
title Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_full Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_fullStr Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_full_unstemmed Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_short Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_sort synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
title_unstemmed Synthesis of intramolecularly cyclized poly(phenylene sulfide)s of the thianthrene‐type
topic Materials Chemistry, Organic Chemistry, Polymers and Plastics
url http://dx.doi.org/10.1002/pola.1988.080260125