Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units

A series of new hexasubstituted cyclotriphosphazene derivatives with azo linking units, 4a-d have been synthesized. The alkylation reaction of 4-acetamidophenol with alkylbromide (heptyl, nonyl, decyl, and dodecyl) formed 1a-d, which were further reduced to form the corresponding intermediates, 2a-d...

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Main Authors: Zuhair Jamain, Melati Khairuddean, Miyeko Lotus Loh, Nur Liyana Abdul Manaff, Mohamad Zul Hilmey Makmud
Format: Article
Language:English
English
Published: Institut Kimia Malaysia 2020
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Online Access:https://eprints.ums.edu.my/id/eprint/27509/1/Synthesis%20and%20characterization%20of%20hexasubstituted%20cyclotriphosphazene%20derivatives%20with%20azo%20linking%20units%20abstract.pdf
https://eprints.ums.edu.my/id/eprint/27509/2/Synthesis%20and%20Characterization%20of%20Hexasubstituted%20Cyclotriphosphazene%20Derivatives%20with%20Azo%20Linking%20Units%20fulltext.pdf
https://eprints.ums.edu.my/id/eprint/27509/
https://ikm.org.my/ojs/index.php/MJChem/article/view/795/356
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spelling my.ums.eprints.275092021-06-30T11:04:42Z https://eprints.ums.edu.my/id/eprint/27509/ Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units Zuhair Jamain Melati Khairuddean Miyeko Lotus Loh Nur Liyana Abdul Manaff Mohamad Zul Hilmey Makmud QC Physics A series of new hexasubstituted cyclotriphosphazene derivatives with azo linking units, 4a-d have been synthesized. The alkylation reaction of 4-acetamidophenol with alkylbromide (heptyl, nonyl, decyl, and dodecyl) formed 1a-d, which were further reduced to form the corresponding intermediates, 2a-d. The diazotization reaction of 2a-d with phenol formed calamitic compounds, 3a-d with the azo group later reacted with hexachlorocyclotriphosphazene (HCCP) to yield the final compounds, 4a-d. The functional groups of all the compounds were determined using Fourier Transform Infrared (FTIR), while their molecular structures were characterized by Nuclear Magnetic Resonance (NMR) spectroscopy. The purity of these compounds was confirmed using CHN elemental analysis. Polarized Optical Microscopy (POM) was used to determine the liquid crystal properties of the synthesized compounds. The rod-like intermediates, 3a-d and the disc-like hexasubstituted final products, 4a-d were found to be non-mesogenic without any liquid crystal properties. The results showed that the introduction of non-mesogenic intermediate sidearms would eventually give non-mesogenic products. All the final compounds showed the clearing temperature in the range of 120-130°C. Institut Kimia Malaysia 2020 Article PeerReviewed text en https://eprints.ums.edu.my/id/eprint/27509/1/Synthesis%20and%20characterization%20of%20hexasubstituted%20cyclotriphosphazene%20derivatives%20with%20azo%20linking%20units%20abstract.pdf text en https://eprints.ums.edu.my/id/eprint/27509/2/Synthesis%20and%20Characterization%20of%20Hexasubstituted%20Cyclotriphosphazene%20Derivatives%20with%20Azo%20Linking%20Units%20fulltext.pdf Zuhair Jamain and Melati Khairuddean and Miyeko Lotus Loh and Nur Liyana Abdul Manaff and Mohamad Zul Hilmey Makmud (2020) Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units. Malaysian Journal of Chemistry, 22 (4). pp. 125-140. ISSN 1511-2292 https://ikm.org.my/ojs/index.php/MJChem/article/view/795/356
institution Universiti Malaysia Sabah
building UMS Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sabah
content_source UMS Institutional Repository
url_provider http://eprints.ums.edu.my/
language English
English
topic QC Physics
spellingShingle QC Physics
Zuhair Jamain
Melati Khairuddean
Miyeko Lotus Loh
Nur Liyana Abdul Manaff
Mohamad Zul Hilmey Makmud
Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units
description A series of new hexasubstituted cyclotriphosphazene derivatives with azo linking units, 4a-d have been synthesized. The alkylation reaction of 4-acetamidophenol with alkylbromide (heptyl, nonyl, decyl, and dodecyl) formed 1a-d, which were further reduced to form the corresponding intermediates, 2a-d. The diazotization reaction of 2a-d with phenol formed calamitic compounds, 3a-d with the azo group later reacted with hexachlorocyclotriphosphazene (HCCP) to yield the final compounds, 4a-d. The functional groups of all the compounds were determined using Fourier Transform Infrared (FTIR), while their molecular structures were characterized by Nuclear Magnetic Resonance (NMR) spectroscopy. The purity of these compounds was confirmed using CHN elemental analysis. Polarized Optical Microscopy (POM) was used to determine the liquid crystal properties of the synthesized compounds. The rod-like intermediates, 3a-d and the disc-like hexasubstituted final products, 4a-d were found to be non-mesogenic without any liquid crystal properties. The results showed that the introduction of non-mesogenic intermediate sidearms would eventually give non-mesogenic products. All the final compounds showed the clearing temperature in the range of 120-130°C.
format Article
author Zuhair Jamain
Melati Khairuddean
Miyeko Lotus Loh
Nur Liyana Abdul Manaff
Mohamad Zul Hilmey Makmud
author_facet Zuhair Jamain
Melati Khairuddean
Miyeko Lotus Loh
Nur Liyana Abdul Manaff
Mohamad Zul Hilmey Makmud
author_sort Zuhair Jamain
title Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units
title_short Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units
title_full Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units
title_fullStr Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units
title_full_unstemmed Synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units
title_sort synthesis and characterization of hexasubstituted cyclotriphosphazene derivatives with azo linking units
publisher Institut Kimia Malaysia
publishDate 2020
url https://eprints.ums.edu.my/id/eprint/27509/1/Synthesis%20and%20characterization%20of%20hexasubstituted%20cyclotriphosphazene%20derivatives%20with%20azo%20linking%20units%20abstract.pdf
https://eprints.ums.edu.my/id/eprint/27509/2/Synthesis%20and%20Characterization%20of%20Hexasubstituted%20Cyclotriphosphazene%20Derivatives%20with%20Azo%20Linking%20Units%20fulltext.pdf
https://eprints.ums.edu.my/id/eprint/27509/
https://ikm.org.my/ojs/index.php/MJChem/article/view/795/356
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score 13.189132