File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Synthesis and properties of novel aromatic polyimides derived from bis(p-aminophenoxy)methylphenylsilane

TitleSynthesis and properties of novel aromatic polyimides derived from bis(p-aminophenoxy)methylphenylsilane
Authors
Issue Date1997
Citation
Journal of Applied Polymer Science, 1997, v. 63, n. 3, p. 369-376 How to Cite?
AbstractA novel siloxane-containing diamine, bis(p-aminophenoxy)methylphenylsilane (BAMPS), was synthesized from the condensation of dichloromethylphenylsilane with p-aminophenol in the presence of triethylamine. A series of BAMPS-based aromatic polyimides were prepared from BAMPS and various aromatic tetracarboxylic dianhydrides by the usual two-step procedure including ring-opening polyaddition to poly(amic acid)s and subsequent cyclodehydration to polyimides. The inherent viscosities of poly(amic acid)s III -III ranged from 0.09 to 0.36 dL g in N,N-dimethylacetamide at a concentration of 0.5 g dL at 30°C. The inherent viscosities of polyimides were between 0.06 and 0.32 dL g in various solvents at 30°C. Polyimides, especially IV and IV were soluble in a wide range of organic solvents such as N-methyl-2-pyrrolidinone, concentrated H SO . N.N-dimethylacetamide, N.N-dimethylfomamide, and dimethyl sulfoxide. The polyimides were characterized by elementary analysis, IR spectra. TGA, and DSC. They also had glass transition temperatures ranging from 128 to 181°C. The 10% mass loas temperature was recorded in the range of 404-443°C in nitrogen and of 315-339°C in oxygen. © 1997 John Wiley & Sons. Inc. a f c b 2 4 -1 -1 -1
Persistent Identifierhttp://hdl.handle.net/10722/297993
ISSN
2023 Impact Factor: 2.7
2023 SCImago Journal Rankings: 0.557
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiaw, Der Jang-
dc.contributor.authorYang, Wen Chung Ou-
dc.contributor.authorLi, Lain Jong-
dc.contributor.authorYang, Mei Hui-
dc.date.accessioned2021-04-08T03:07:25Z-
dc.date.available2021-04-08T03:07:25Z-
dc.date.issued1997-
dc.identifier.citationJournal of Applied Polymer Science, 1997, v. 63, n. 3, p. 369-376-
dc.identifier.issn0021-8995-
dc.identifier.urihttp://hdl.handle.net/10722/297993-
dc.description.abstractA novel siloxane-containing diamine, bis(p-aminophenoxy)methylphenylsilane (BAMPS), was synthesized from the condensation of dichloromethylphenylsilane with p-aminophenol in the presence of triethylamine. A series of BAMPS-based aromatic polyimides were prepared from BAMPS and various aromatic tetracarboxylic dianhydrides by the usual two-step procedure including ring-opening polyaddition to poly(amic acid)s and subsequent cyclodehydration to polyimides. The inherent viscosities of poly(amic acid)s III -III ranged from 0.09 to 0.36 dL g in N,N-dimethylacetamide at a concentration of 0.5 g dL at 30°C. The inherent viscosities of polyimides were between 0.06 and 0.32 dL g in various solvents at 30°C. Polyimides, especially IV and IV were soluble in a wide range of organic solvents such as N-methyl-2-pyrrolidinone, concentrated H SO . N.N-dimethylacetamide, N.N-dimethylfomamide, and dimethyl sulfoxide. The polyimides were characterized by elementary analysis, IR spectra. TGA, and DSC. They also had glass transition temperatures ranging from 128 to 181°C. The 10% mass loas temperature was recorded in the range of 404-443°C in nitrogen and of 315-339°C in oxygen. © 1997 John Wiley & Sons. Inc. a f c b 2 4 -1 -1 -1-
dc.languageeng-
dc.relation.ispartofJournal of Applied Polymer Science-
dc.titleSynthesis and properties of novel aromatic polyimides derived from bis(p-aminophenoxy)methylphenylsilane-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1002/(SICI)1097-4628(19970118)63:3<369::AID-APP13>3.0.CO;2-W-
dc.identifier.scopuseid_2-s2.0-0030833162-
dc.identifier.volume63-
dc.identifier.issue3-
dc.identifier.spage369-
dc.identifier.epage376-
dc.identifier.isiWOS:A1997VZ93000013-
dc.identifier.issnl0021-8995-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats