Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones

Kajian ini dimulakan dengan sintesis dan pencirian dua siri utama bahan pemula: pengalkilan naftaldehid (2-8) dan pengasetilan kumarin tertukar ganti (9-11). Bahan pemula yang diperoleh dikenalpasti melalui kaedah spektroskopi seperti inframerah transformasi Fourier (FTIR), resonans magnet nukleus (...

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Main Author: Lim , Sumithda Yeong Hui
Format: Thesis
Language:English
Published: 2016
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Online Access:http://eprints.usm.my/31375/1/SUMITHDA_LIM_YEONG_HUI_24.pdf
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spelling my-usm-ep.313752019-04-12T05:25:23Z Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones 2016-03 Lim , Sumithda Yeong Hui QC1 Physics (General) Kajian ini dimulakan dengan sintesis dan pencirian dua siri utama bahan pemula: pengalkilan naftaldehid (2-8) dan pengasetilan kumarin tertukar ganti (9-11). Bahan pemula yang diperoleh dikenalpasti melalui kaedah spektroskopi seperti inframerah transformasi Fourier (FTIR), resonans magnet nukleus (NMR) dan mikroanalisis CHN. Analisa pembelauan sinar-X hablur tunggal (XRD) juga dijalankan dengan hablur bagi sebatian 3, 34, dan 41 menghablur dalam sistem kristal triklinik. Lima siri kalkon kemudiannya disintesis melalui kaedah kondensasi Claisen-Schmidt dengan tiga siri diterbitkan daripada kumarin asetil tertukar ganti (12-33) dan dua siri yang lain diterbitkan daripada asetofenon tertukar ganti (34-46). Semua kalkon yang disintesis telah dicirikan dengan analisa unsur (CHN), spektroskopi FTIR , 1H-NMR, 13C-NMR, DEPT 135, 1H-1H COSY, 1H-13C HMQC dan 1H-13C HMBC. Kalkon 23, 28, 34, dan 41 telah dipilih untuk analisis kristolografi. This study was started by the synthesis and characterization of two main series of starting materials: alkylation of naphthaldehydes (2-8) and acetylation of substituted coumarins (9-11). The starting materials thus obtained were elucidated by the spectroscopic methods such as fourier transform infrared (FTIR), nuclear magnetic resonance (NMR) and CHN microanalyses. Single crystal X-ray diffraction (XRD) analyses have also been carried out wherein the crystals of compound 3, 34 and 41 crystallized in a triclinic crystal system. Five novel series of chalcones were subsequently synthesized by means of Claisen-Schmidt condensation wherein three series were derived from substituted acetyl coumarins (12-33) and the remaining two series was derived from substituted acetophenones (34-46). All the synthesized chalcones were characterized by elemental analysis (CHN), FTIR, 1H-NMR, 13C-NMR, DEPT 135, 1H-1H COSY, 1H-13C HMQC and 1H-13C HMBC spectroscopy. Selected chalcones, 23, 28, 34, and 41 were selected for crystallography analysis. 2016-03 Thesis http://eprints.usm.my/31375/ http://eprints.usm.my/31375/1/SUMITHDA_LIM_YEONG_HUI_24.pdf application/pdf en public masters Universiti Sains Malaysia Pusat Pengajian Sains Fizik (School of Physics)
institution Universiti Sains Malaysia
collection USM Institutional Repository
language English
topic QC1 Physics (General)
spellingShingle QC1 Physics (General)
Lim , Sumithda Yeong Hui
Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones
description Kajian ini dimulakan dengan sintesis dan pencirian dua siri utama bahan pemula: pengalkilan naftaldehid (2-8) dan pengasetilan kumarin tertukar ganti (9-11). Bahan pemula yang diperoleh dikenalpasti melalui kaedah spektroskopi seperti inframerah transformasi Fourier (FTIR), resonans magnet nukleus (NMR) dan mikroanalisis CHN. Analisa pembelauan sinar-X hablur tunggal (XRD) juga dijalankan dengan hablur bagi sebatian 3, 34, dan 41 menghablur dalam sistem kristal triklinik. Lima siri kalkon kemudiannya disintesis melalui kaedah kondensasi Claisen-Schmidt dengan tiga siri diterbitkan daripada kumarin asetil tertukar ganti (12-33) dan dua siri yang lain diterbitkan daripada asetofenon tertukar ganti (34-46). Semua kalkon yang disintesis telah dicirikan dengan analisa unsur (CHN), spektroskopi FTIR , 1H-NMR, 13C-NMR, DEPT 135, 1H-1H COSY, 1H-13C HMQC dan 1H-13C HMBC. Kalkon 23, 28, 34, dan 41 telah dipilih untuk analisis kristolografi. This study was started by the synthesis and characterization of two main series of starting materials: alkylation of naphthaldehydes (2-8) and acetylation of substituted coumarins (9-11). The starting materials thus obtained were elucidated by the spectroscopic methods such as fourier transform infrared (FTIR), nuclear magnetic resonance (NMR) and CHN microanalyses. Single crystal X-ray diffraction (XRD) analyses have also been carried out wherein the crystals of compound 3, 34 and 41 crystallized in a triclinic crystal system. Five novel series of chalcones were subsequently synthesized by means of Claisen-Schmidt condensation wherein three series were derived from substituted acetyl coumarins (12-33) and the remaining two series was derived from substituted acetophenones (34-46). All the synthesized chalcones were characterized by elemental analysis (CHN), FTIR, 1H-NMR, 13C-NMR, DEPT 135, 1H-1H COSY, 1H-13C HMQC and 1H-13C HMBC spectroscopy. Selected chalcones, 23, 28, 34, and 41 were selected for crystallography analysis.
format Thesis
qualification_level Master's degree
author Lim , Sumithda Yeong Hui
author_facet Lim , Sumithda Yeong Hui
author_sort Lim , Sumithda Yeong Hui
title Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones
title_short Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones
title_full Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones
title_fullStr Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones
title_full_unstemmed Synthesis, Characterization And Biological Evaluation Of Naphthalene - And Coumarin-Based Chalcones
title_sort synthesis, characterization and biological evaluation of naphthalene - and coumarin-based chalcones
granting_institution Universiti Sains Malaysia
granting_department Pusat Pengajian Sains Fizik (School of Physics)
publishDate 2016
url http://eprints.usm.my/31375/1/SUMITHDA_LIM_YEONG_HUI_24.pdf
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