Date of Award

1-1-2012

Thesis Type

masters

Document Type

Thesis

Divisions

science

Department

Dept of Chemistry

Institution

University of Malaya

Abstract

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.

Note

Dissertation Submitted In fulfillment Of The Requirements For The Degree Of Master Of Science

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