Home
GSC Advanced Research and Reviews
Peer-reviewed | Multidisciplinary Journal | Impact factor 8.3 | ISSN: 2582-4597 | Crossref DOI

Main navigation

  • Home
    • Journal Information
    • Editorial Board Members
    • Reviewer Panel
    • Abstracting and Indexing
    • Journal Policies
    • Our CrossMark Policy
    • Publication Ethics
    • Issue in Progress
    • Current Issue
    • Past Issues
    • Instructions for Authors
    • Article processing fee
    • Track Manuscript Status
    • Get Publication Certificate
    • Join Editorial Board
    • Join Reviewer Panel
  • Contact us
  • Downloads

Selective mono substitution of cyclotri-phosphazene by 2-Hydroxyethylacrylate producing new acrylate cyclo-triphosphazene

Breadcrumb

  • Home
  • Selective Mono Substitution of Cyclotri-phosphazene By 2-Hydroxyethylacrylate Producing New Acrylate Cyclo-triphosphazene
  • Selective mono substitution of cyclotri-phosphazene by 2-Hydroxyethylacrylate producing new acrylate cyclo-triphosphazene

Maha F. Abbass 1, *, Salah Al-Shukri 1 and Ahmed A. Ahmed 2

1 Department of Chemistry, College of Science, Mustansiriyah University, Baghdad 10052, Iraq.
2 Polymer Research Unit, College of Science, Al-Mustansiriyah University, Baghdad 10052, Iraq. 
 
Research Article
GSC Advanced Research and Reviews, 2022, 10(03), 080–087.
Article DOI: 10.30574/gscarr.2022.10.3.0070
DOI url: https://doi.org/10.30574/gscarr.2022.10.3.0070
Received on 04 February 2022; revised on 12 March 2022; accepted on 14 March 2022
 
In this work, new acrylate cyclotriphosphazene moiety (PN-A) was successfully synthesized starting from cyclotriphosphazene (PN) compound. This compound reacted with 2-hydroxyethylacrylate utilizing 1:1 mole ratio to increase the priority of one substitution reaction and forming PN-A molecule. The crud product was purified by recrystallization using n-hexane and column chromatography using cyclohexane: ethyl acetate 60:40 mL ratio as eluent. The obtained pure target product was characterized using FTIR, 1H NMR, 13C NMR, and 31P NMR techniques. All spectra demonstrates the chemical structure of the product hence the showed all required peaks to identify it.
 
Cyclotriphosphazene; Column chromatography; 1H NMR; 31P NMR; Acrylate
 
https://gscarr.gsconlinepress.com/sites/default/files/fulltext_pdf/GSCARR-2022-…

Preview Article PDF

Maha F. Abbass, Salah Al-Shukri and Ahmed A. Ahmed. Selective mono substitution of cyclotri-phosphazene by 2-Hydroxyethylacrylate producing new acrylate cyclo-triphosphazene. GSC Advanced Research and Reviews, 2022, 10(3), 080-087. Article DOI: https://doi.org/10.30574/gscarr.2022.10.3.0070

Copyright © Author(s). All rights reserved. This article is published under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, sharing, adaptation, distribution, and reproduction in any medium or format, as long as appropriate credit is given to the original author(s) and source, a link to the license is provided, and any changes made are indicated.


All statements, opinions, and data contained in this publication are solely those of the individual author(s) and contributor(s). The journal, editors, reviewers, and publisher disclaim any responsibility or liability for the content, including accuracy, completeness, or any consequences arising from its use.

Get Certificates

Get Publication Certificate

Download LoA

Check Corssref DOI details

Issue details

Issue Cover Page

Editorial Board

Table of content

Copyright © 2026 GSC Advanced Research and Reviews - All rights reserved

Developed & Designed by VS Infosolution