Synthesis of phenol formaldehyde-containing pendant itaconamic, itaconimide and poly[N-(substituted) itaconimides].
Saved in:
| Title: | Synthesis of phenol formaldehyde-containing pendant itaconamic, itaconimide and poly[N-(substituted) itaconimides]. |
|---|---|
| Authors: | Pyriadi, Thanun M., Berzinji, Azad S. |
| Source: | Designed Monomers & Polymers. 2003, Vol. 6 Issue 1, p115-122. 8p. |
| Subjects: | Formaldehyde, Phenols, Gums & resins |
| Abstract: | Ortho- and meta-aminophenols were allowed to react with itaconic anhydride, forming N-ortho- and N-meta-hydroxyphenyl itaconamic acids in good yields. The above substituted itaconamic acids were allowed to react with formaldehyde in conditions similar to those of Novolac preparation and novel phenol formaldehyde resins were obtained having pendant itaconamic acids. Similarly, formaldehyde was allowed to react with N-ortho- and N-meta-hydroxyphenyl itaconimides, producing novel resins. Furthermore, the itacon vinyls of the pendant groups of itaconamic acids as well as their corresponding imides were polymerized free radically using AIBN as an initiator and tough cross-linked resins were obtained. [ABSTRACT FROM AUTHOR] |
| Copyright of Designed Monomers & Polymers is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Links: – Type: pdflink Text: Availability: 0 |
|---|---|
| Header | DbId: egs DbLabel: Engineering Source An: 9079628 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
| IllustrationInfo | |
| Items | – Name: Title Label: Title Group: Ti Data: Synthesis of phenol formaldehyde-containing pendant itaconamic, itaconimide and poly[N-(substituted) itaconimides]. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Pyriadi%2C+Thanun+M%2E%22">Pyriadi, Thanun M.</searchLink><br /><searchLink fieldCode="AR" term="%22Berzinji%2C+Azad+S%2E%22">Berzinji, Azad S.</searchLink> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Designed+Monomers+%26+Polymers%22">Designed Monomers & Polymers</searchLink>. 2003, Vol. 6 Issue 1, p115-122. 8p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Formaldehyde%22">Formaldehyde</searchLink><br /><searchLink fieldCode="DE" term="%22Phenols%22">Phenols</searchLink><br /><searchLink fieldCode="DE" term="%22Gums+%26+resins%22">Gums & resins</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Ortho- and meta-aminophenols were allowed to react with itaconic anhydride, forming N-ortho- and N-meta-hydroxyphenyl itaconamic acids in good yields. The above substituted itaconamic acids were allowed to react with formaldehyde in conditions similar to those of Novolac preparation and novel phenol formaldehyde resins were obtained having pendant itaconamic acids. Similarly, formaldehyde was allowed to react with N-ortho- and N-meta-hydroxyphenyl itaconimides, producing novel resins. Furthermore, the itacon vinyls of the pendant groups of itaconamic acids as well as their corresponding imides were polymerized free radically using AIBN as an initiator and tough cross-linked resins were obtained. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Designed Monomers & Polymers is the property of Taylor & Francis Ltd and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
| PLink | https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=egs&AN=9079628 |
| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1163/156855503321127583 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 8 StartPage: 115 Subjects: – SubjectFull: Formaldehyde Type: general – SubjectFull: Phenols Type: general – SubjectFull: Gums & resins Type: general Titles: – TitleFull: Synthesis of phenol formaldehyde-containing pendant itaconamic, itaconimide and poly[N-(substituted) itaconimides]. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Pyriadi, Thanun M. – PersonEntity: Name: NameFull: Berzinji, Azad S. IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 03 Text: 2003 Type: published Y: 2003 Identifiers: – Type: issn-print Value: 1385772X Numbering: – Type: volume Value: 6 – Type: issue Value: 1 Titles: – TitleFull: Designed Monomers & Polymers Type: main |
| ResultId | 1 |
