Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/434815
Title: Synthesis of poly nuclear hetero aryl substituted novel terpyridine scaffold and their metal complexes Study on their interaction with ct DNA
Researcher: Desai Dipen Harishbhai
Guide(s): Patel Paresh N
Keywords: Applied Sciences
Chemistry
Poly nuclear science
University: Uka Tarsadia University
Completed Date: 2022
Abstract: The photoluminescence molecules have very unique importance in the advancement of science and technology. Here, we studied the poly-nuclear and hetero-aryl substituted novel terpyridine scaffolds.These designed moieties were synthesized by multicomponent condensation reactions with various acetyl pyridine derivatives in the presence of NH4OHand KOH. We have developed the unique protocol to synthesis highly substituted pyridine scaffolds that are not easily accessed by conventional methods. The structures of all newly prepared terpyridine molecules have been well established by preforming various spectral analysessuch as IR, NMR, DEPT, HRMS and single crystal XRD studies for selected molecules. Metal complexes of the terpyridine derivative obtained from 2- acetylpyridine were synthesized by reaction with various transition metals and lanthanides. Structures of all the prepared metal complexes were characterized by IR, MASS and single-crystal X-ray analysis for selected molecules. UV-visible and florescence spectra were recorded for all the synthesized compounds.The prepared scaffolds as such and their metal complexes may provide an efficient candidate for photo-luminescent chemistry.To check the possibility of medical application of prepared molecules, all the compounds were studied for their ct-DNA binding studies by UV absorption and emission spectrometry. The obtained results shown that all these molecules have good binding affinity with ct-DNA. newline
Pagination: xix,205p
URI: http://hdl.handle.net/10603/434815
Appears in Departments:Faculty of Applied Science

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02_preliminary pages.pdf1.49 MBAdobe PDFView/Open
03_content.pdf270.66 kBAdobe PDFView/Open
04_abstract.pdf43.45 kBAdobe PDFView/Open
05_chapter 1.pdf1.56 MBAdobe PDFView/Open
06_chapter 2.pdf3.64 MBAdobe PDFView/Open
07_chapter 3.pdf2.18 MBAdobe PDFView/Open
08_chapter 4.pdf3.74 MBAdobe PDFView/Open
09_chapter 5.pdf2.19 MBAdobe PDFView/Open
10_annexures.pdf157.44 kBAdobe PDFView/Open
80_recommendation.pdf440.98 kBAdobe PDFView/Open
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