Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/4257
Title: Exploration and development of benzimidazole-based phosphine ligands towards suzuki-miyaura cross-coupling
Authors: Yeung, Chung-chiu
Keywords: Hong Kong Polytechnic University -- Dissertations
Ligands (Biochemistry)
Benzimidazoles
Issue Date: 2010
Publisher: The Hong Kong Polytechnic University
Abstract: The research study is focused on the development of easily accessible heterocyclic phosphine ligands. The first part of the investigation is the attempted study of electronic effects towards the reactivity of indolyl phosphine ligands while the second part is the design and synthesis of newly developed benzimidazole-based phosphine ligands and their applications on Suzuki-Miyaura Coupling. In the study of indolyl phosphine ligand, we tried to examine the electronic effect by the incorporation of different substituted groups on the 5-position of the indole ring on the ligand template. We aim to study the importance of the electronic density on the phosphorus atom over the reactivity of the ligands. We propose that the reactivity of the ligands should be directly proportional to the electron density of P donor atom of ligands. A family of 5-substituted indolyl phosphine ligands were successfully prepared and their reactivity was compared by the same Suzuki coupling reaction under mild reaction conditions in order to demonstrate their reactivity differences. We believe this research findings will contribute to the future development of related ligands. In my second project, a new scaffold, benzimidazole, was used for the ligand design. Benzimidazole is attractive as it is commercially available with a reasonable price. In addition, the synthesis of benzimidazole-based phosphine ligand is atom economic that less side products are formed. However, using ligands with benzimidazole scaffold is not electron-rich enough for Suzuki coupling. Based on the research concept of my first project, we modified the ligand design by adding two methyl groups on the benzimidazole scaffold. The new dimethyl benzimidazole-based phosphine ligand is highly effective for Suzuki coupling of both activated and deactivated aryl chlorides with moderate catalytst loading.
Description: 218 leaves : ill. ; 30 cm.
PolyU Library Call No.: [THS] LG51 .H577M ABCT 2010 Yeung
URI: http://hdl.handle.net/10397/4257
Rights: All rights reserved.
Appears in Collections:Thesis

Files in This Item:
File Description SizeFormat 
b24250247_link.htmFor PolyU Users 162 BHTMLView/Open
b24250247_ir.pdfFor All Users (Non-printable) 9.93 MBAdobe PDFView/Open
Show full item record

Page view(s)

399
Last Week
2
Last month
Checked on Jan 15, 2017

Download(s)

311
Checked on Jan 15, 2017

Google ScholarTM

Check



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.