Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II)

This project was aimed to synthesize the allylideneamine moiety ligand in order to replace the phenylpyridine (ppy) moiety ligand in the metallacycle complexes. The L series compounds were synthesized by reacting p-(R)-acetophenone (R = H or NO2) to glyoxal through cross-adol condensation reactio...

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Main Author: Ong, Cheng Guan
Format: Final Year Project Report
Language:English
English
Published: Universiti Malaysia Sarawak (UNIMAS) 2012
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Online Access:http://ir.unimas.my/id/eprint/26352/1/Modification%20of%20%CE%B1%2C%CE%B2-conjugated%2024pgs.pdf
http://ir.unimas.my/id/eprint/26352/4/Ong%20Cheng%20Guan.pdf
http://ir.unimas.my/id/eprint/26352/
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spelling my.unimas.ir.263522024-02-21T02:27:05Z http://ir.unimas.my/id/eprint/26352/ Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II) Ong, Cheng Guan Q Science (General) QD Chemistry This project was aimed to synthesize the allylideneamine moiety ligand in order to replace the phenylpyridine (ppy) moiety ligand in the metallacycle complexes. The L series compounds were synthesized by reacting p-(R)-acetophenone (R = H or NO2) to glyoxal through cross-adol condensation reaction. Then, three S series compounds were synthesized by adding 2-aminophenol into the L series compounds using Schiff base synthesis reaction. Two of the S series compounds namely S1 and S2 were not obtained in the synthesis; indeed, another product namely S4 was obtained from the reaction of remaining glyoxal and 2-aminophenol. Two Co2+ complexes were prepared from the reaction of respective S4 and S3 compounds to CoCl2 at room temperature and the spectroscopic data from NMR, IR and UV were obtained. There are some changes found in the IR, 1H NMR and UV-visible spectra of complexes compared to their free ligand. The conductivity studies showed that the oxidation states of the complexes were remained at +2 oxidation state and all complexes are neutral complex. Universiti Malaysia Sarawak (UNIMAS) 2012 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/26352/1/Modification%20of%20%CE%B1%2C%CE%B2-conjugated%2024pgs.pdf text en http://ir.unimas.my/id/eprint/26352/4/Ong%20Cheng%20Guan.pdf Ong, Cheng Guan (2012) Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II). [Final Year Project Report] (Unpublished)
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
English
topic Q Science (General)
QD Chemistry
spellingShingle Q Science (General)
QD Chemistry
Ong, Cheng Guan
Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II)
description This project was aimed to synthesize the allylideneamine moiety ligand in order to replace the phenylpyridine (ppy) moiety ligand in the metallacycle complexes. The L series compounds were synthesized by reacting p-(R)-acetophenone (R = H or NO2) to glyoxal through cross-adol condensation reaction. Then, three S series compounds were synthesized by adding 2-aminophenol into the L series compounds using Schiff base synthesis reaction. Two of the S series compounds namely S1 and S2 were not obtained in the synthesis; indeed, another product namely S4 was obtained from the reaction of remaining glyoxal and 2-aminophenol. Two Co2+ complexes were prepared from the reaction of respective S4 and S3 compounds to CoCl2 at room temperature and the spectroscopic data from NMR, IR and UV were obtained. There are some changes found in the IR, 1H NMR and UV-visible spectra of complexes compared to their free ligand. The conductivity studies showed that the oxidation states of the complexes were remained at +2 oxidation state and all complexes are neutral complex.
format Final Year Project Report
author Ong, Cheng Guan
author_facet Ong, Cheng Guan
author_sort Ong, Cheng Guan
title Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II)
title_short Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II)
title_full Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II)
title_fullStr Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II)
title_full_unstemmed Modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with Co(II)
title_sort modification of α,β-conjugated enol-keto containing compound towards to the synthesis of ethyleneimine compound and its complexes with co(ii)
publisher Universiti Malaysia Sarawak (UNIMAS)
publishDate 2012
url http://ir.unimas.my/id/eprint/26352/1/Modification%20of%20%CE%B1%2C%CE%B2-conjugated%2024pgs.pdf
http://ir.unimas.my/id/eprint/26352/4/Ong%20Cheng%20Guan.pdf
http://ir.unimas.my/id/eprint/26352/
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