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Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline

4-((4-nonylphenyl)diazenyl)aniline and 4-(4-decylphenyl)diazenyl)aniline are an azo compounds with different terminal chains. The synthesis process was started via diazotization of 4- nitroaniline with phenol formed 4-(4-nitrophenyl)phenol (1). After that, 4-(4-nitrophenyl)phenol was alkylated with...

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Main Authors: S. Habil, Zuhair Jamain, Mohamad Zul Hilmey Makmud
Format: Proceedings
Language:English
English
Published: Faculty of Science and Natural Resources 2021
Subjects:
QD1-999 Chemistry
Online Access:https://eprints.ums.edu.my/id/eprint/32126/1/Synthesis%20and%20chemical%20interpretation%20of%204-%28%284-nonylphenyl%29%20diazenyl%29%20aniline%20and%204-%28%284-decylphenyl%29%20diazenyl%29%20aniline.ABSTRCT.pdf
https://eprints.ums.edu.my/id/eprint/32126/2/SYNTHESIS%20AND%20CHEMICAL%20INTERPRETATION%20OF%204-%28%284-%20NONYLPHENYL%29%20DIAZENYL%29%20ANILINE%20AND%204-%28%284-DECYLPHENYL%29%20DIAZENYL%29%20ANILINE.pdf
https://eprints.ums.edu.my/id/eprint/32126/
https://drive.google977-2-73-522200-2.com/file/d/1zKEpSiYvg9vZHHzuKra49512D_AMLubu/view
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spelling my.ums.eprints.321262022-03-31T06:04:29Z https://eprints.ums.edu.my/id/eprint/32126/ Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline S. Habil Zuhair Jamain Mohamad Zul Hilmey Makmud QD1-999 Chemistry 4-((4-nonylphenyl)diazenyl)aniline and 4-(4-decylphenyl)diazenyl)aniline are an azo compounds with different terminal chains. The synthesis process was started via diazotization of 4- nitroaniline with phenol formed 4-(4-nitrophenyl)phenol (1). After that, 4-(4-nitrophenyl)phenol was alkylated with 1-bromononane and 1-bromodecane to yield 1-(4-nitrophenyl)-2-(4-nonylphenyl)diazene (2) and 1-(4-decylphenyl)-2-(4-nitrophenyl)diazene (3), respectively. Finally, both molecules will undergo reduction to yield 4-((4-nonylphenyl)diazenyl)aniline (4) and 4-(4-decylphenyl)diazenyl)aniline (5), respectively. These two compounds were submitted to extensive spectroscopic examination, including Fourier Transform-Infrared (FT-IR) and Nuclear Magnetic Resonance (NMR). Faculty of Science and Natural Resources 2021-10 Proceedings PeerReviewed text en https://eprints.ums.edu.my/id/eprint/32126/1/Synthesis%20and%20chemical%20interpretation%20of%204-%28%284-nonylphenyl%29%20diazenyl%29%20aniline%20and%204-%28%284-decylphenyl%29%20diazenyl%29%20aniline.ABSTRCT.pdf text en https://eprints.ums.edu.my/id/eprint/32126/2/SYNTHESIS%20AND%20CHEMICAL%20INTERPRETATION%20OF%204-%28%284-%20NONYLPHENYL%29%20DIAZENYL%29%20ANILINE%20AND%204-%28%284-DECYLPHENYL%29%20DIAZENYL%29%20ANILINE.pdf S. Habil and Zuhair Jamain and Mohamad Zul Hilmey Makmud (2021) Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline. https://drive.google977-2-73-522200-2.com/file/d/1zKEpSiYvg9vZHHzuKra49512D_AMLubu/view
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 QD1-999 Chemistry
spellingShingle QD1-999 Chemistry
S. Habil
Zuhair Jamain
Mohamad Zul Hilmey Makmud
Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline
description 4-((4-nonylphenyl)diazenyl)aniline and 4-(4-decylphenyl)diazenyl)aniline are an azo compounds with different terminal chains. The synthesis process was started via diazotization of 4- nitroaniline with phenol formed 4-(4-nitrophenyl)phenol (1). After that, 4-(4-nitrophenyl)phenol was alkylated with 1-bromononane and 1-bromodecane to yield 1-(4-nitrophenyl)-2-(4-nonylphenyl)diazene (2) and 1-(4-decylphenyl)-2-(4-nitrophenyl)diazene (3), respectively. Finally, both molecules will undergo reduction to yield 4-((4-nonylphenyl)diazenyl)aniline (4) and 4-(4-decylphenyl)diazenyl)aniline (5), respectively. These two compounds were submitted to extensive spectroscopic examination, including Fourier Transform-Infrared (FT-IR) and Nuclear Magnetic Resonance (NMR).
format Proceedings
author S. Habil
Zuhair Jamain
Mohamad Zul Hilmey Makmud
author_facet S. Habil
Zuhair Jamain
Mohamad Zul Hilmey Makmud
author_sort S. Habil
title Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline
title_short Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline
title_full Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline
title_fullStr Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline
title_full_unstemmed Synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline
title_sort synthesis and chemical interpretation of 4-((4-nonylphenyl) diazenyl) aniline and 4-((4-decylphenyl) diazenyl) aniline
publisher Faculty of Science and Natural Resources
publishDate 2021
url https://eprints.ums.edu.my/id/eprint/32126/1/Synthesis%20and%20chemical%20interpretation%20of%204-%28%284-nonylphenyl%29%20diazenyl%29%20aniline%20and%204-%28%284-decylphenyl%29%20diazenyl%29%20aniline.ABSTRCT.pdf
https://eprints.ums.edu.my/id/eprint/32126/2/SYNTHESIS%20AND%20CHEMICAL%20INTERPRETATION%20OF%204-%28%284-%20NONYLPHENYL%29%20DIAZENYL%29%20ANILINE%20AND%204-%28%284-DECYLPHENYL%29%20DIAZENYL%29%20ANILINE.pdf
https://eprints.ums.edu.my/id/eprint/32126/
https://drive.google977-2-73-522200-2.com/file/d/1zKEpSiYvg9vZHHzuKra49512D_AMLubu/view
_version_ 1760230983988150272
score 13.211869

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