Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan

ii ABSTRACT 2-N-(3-methyl)piperidinoquinoline (25), 2-N-(4-methyl)piperidinoquinoline (26), 2-N-anilinoquinoline (28), 2-N- (m-methyl)anilinoquinoline (30), 2-N-(p-methyl)anilinoquinoline (32), 2-N-(m-ethyl)anilinoquinoline (34), 2-N-(p-ethyl)anilinoquinoline (36), 2-N-methylanilinoquinoline (38),...

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主要作者: Zainal Abidin, Hasan
格式: Thesis
出版: 2012
主题:
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author Zainal Abidin, Hasan
author_facet Zainal Abidin, Hasan
author_sort Zainal Abidin, Hasan
description ii ABSTRACT 2-N-(3-methyl)piperidinoquinoline (25), 2-N-(4-methyl)piperidinoquinoline (26), 2-N-anilinoquinoline (28), 2-N- (m-methyl)anilinoquinoline (30), 2-N-(p-methyl)anilinoquinoline (32), 2-N-(m-ethyl)anilinoquinoline (34), 2-N-(p-ethyl)anilinoquinoline (36), 2-N-methylanilinoquinoline (38), 2-N-ethylanilinoquinoline (40), 2-N-(m-methoxy)anilinoquinoline (42), 2-N-(p-methoxy)anilinoquinoline (44), 2-N-(m-chloro)anilinoquinoline (46), and 2-N-(p-chloro)anilinoquinoline (48) were prepared by reacting 2-chloroquinoline (22) with 3-methylpiperidine (23), 4-methylpiperidine (24), aniline (27), m-toluidine (29), p-toluidine (31), m-ethylaniline (33), p-ethylaniline (35), N-methylaniline (37), N-ethylaniline (39), m-anisidine (41), p-anisidine (43), m-chloroaniline (45) and p-chloroaniline (47) respectively. The structure of these compounds were confirmed using 1H NMR, 13C NMR, infra-red and GCMS. The fluorescence properties were recorded using Luminescence Spectrophotometer. Almost all compounds prepared showed highest fluorescence intensity in less polar solvents and lowest fluorescence intensity in polar protic solvents. Compound 30, 34 and 48 showed higher fluorescence intensity in alkaline and neutral conditions while lower fluorescence intensity was recorded in acidic condition.
format Thesis
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institution Universiti Malaya
publishDate 2012
record_format eprints
spelling oai:studentsrepo.um.edu.my:37532019-01-23T01:16:33Z Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan Zainal Abidin, Hasan QD Chemistry ii ABSTRACT 2-N-(3-methyl)piperidinoquinoline (25), 2-N-(4-methyl)piperidinoquinoline (26), 2-N-anilinoquinoline (28), 2-N- (m-methyl)anilinoquinoline (30), 2-N-(p-methyl)anilinoquinoline (32), 2-N-(m-ethyl)anilinoquinoline (34), 2-N-(p-ethyl)anilinoquinoline (36), 2-N-methylanilinoquinoline (38), 2-N-ethylanilinoquinoline (40), 2-N-(m-methoxy)anilinoquinoline (42), 2-N-(p-methoxy)anilinoquinoline (44), 2-N-(m-chloro)anilinoquinoline (46), and 2-N-(p-chloro)anilinoquinoline (48) were prepared by reacting 2-chloroquinoline (22) with 3-methylpiperidine (23), 4-methylpiperidine (24), aniline (27), m-toluidine (29), p-toluidine (31), m-ethylaniline (33), p-ethylaniline (35), N-methylaniline (37), N-ethylaniline (39), m-anisidine (41), p-anisidine (43), m-chloroaniline (45) and p-chloroaniline (47) respectively. The structure of these compounds were confirmed using 1H NMR, 13C NMR, infra-red and GCMS. The fluorescence properties were recorded using Luminescence Spectrophotometer. Almost all compounds prepared showed highest fluorescence intensity in less polar solvents and lowest fluorescence intensity in polar protic solvents. Compound 30, 34 and 48 showed higher fluorescence intensity in alkaline and neutral conditions while lower fluorescence intensity was recorded in acidic condition. 2012 Thesis NonPeerReviewed application/pdf http://studentsrepo.um.edu.my/3753/1/FRONT_PAGE.pdf application/pdf http://studentsrepo.um.edu.my/3753/2/FRONT_PAGE_2.pdf application/pdf http://studentsrepo.um.edu.my/3753/3/ABSTRACT_dll.pdf application/pdf http://studentsrepo.um.edu.my/3753/4/CHAPTER_1.pdf application/pdf http://studentsrepo.um.edu.my/3753/5/CHAPTER_2.pdf application/pdf http://studentsrepo.um.edu.my/3753/6/CHAPTER_3.pdf application/pdf http://studentsrepo.um.edu.my/3753/7/CHAPTER_4.pdf application/pdf http://studentsrepo.um.edu.my/3753/8/CHAPTER_5.pdf application/pdf http://studentsrepo.um.edu.my/3753/9/References.pdf application/pdf http://studentsrepo.um.edu.my/3753/10/APPENDICES%2C_publications%2C.pdf http://pendeta.um.edu.my/client/default/search/results?qu=Synthesis%2C+characterization+and+fluorescence+properties+of+selected+amino+derivatives+of+quinoline&te= Zainal Abidin, Hasan (2012) Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan. Masters thesis, University of Malaya. http://studentsrepo.um.edu.my/3753/
spellingShingle QD Chemistry
Zainal Abidin, Hasan
Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan
title Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan
title_full Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan
title_fullStr Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan
title_full_unstemmed Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan
title_short Synthesis, characterization and fluorescence properties of selected amino derivatives of quinoline / Zainal Abidin Hasan
title_sort synthesis characterization and fluorescence properties of selected amino derivatives of quinoline zainal abidin hasan
topic QD Chemistry
url-record http://pendeta.um.edu.my/client/default/search/results?qu=Synthesis%2C+characterization+and+fluorescence+properties+of+selected+amino+derivatives+of+quinoline&te=
http://studentsrepo.um.edu.my/3753/
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