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Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks

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서명/저자사항Leveraging 1,2-Azaborine's Distinct Electronic Structure to Access New Building Blocks.
개인저자McConnell, Cameron Reed.
단체저자명Boston College. GSAS - Chemistry.
발행사항[S.l.]: Boston College., 2019.
발행사항Ann Arbor: ProQuest Dissertations & Theses, 2019.
형태사항325 p.
기본자료 저록Dissertations Abstracts International 81-03B.
Dissertation Abstract International
ISBN9781085679114
학위논문주기Thesis (Ph.D.)--Boston College, 2019.
일반주기 Source: Dissertations Abstracts International, Volume: 81-03, Section: B.
Advisor: Liu, Shih-Yuan.
이용제한사항This item must not be sold to any third party vendors.
요약Described herein are three projects that derive from in-depth studies of the distinct electronic structure of monocyclic 1,2-dihydro-1,2-azaborine (heretofore referred to as simply 1,2-azaborine). In the first chapter, the first comprehensive review of the late-stage functionalization methods available for 1,2-azaborines as well as their bicyclic and polycyclic (BN-PAH) counterparts is presented. In the second chapter, the development of a general method for both C4 and C5 functionalization based on the building block approach is described. The distinct electronic structure of 1,2-azaborine enables the chemical separation and further functionalization of C4 and C5 borylated isomers. In the second part, the C4, C5, and C6 isomers of BN-styrene analogues were prepared using the newly developed azaborine building blocks. The corresponding polymers were synthesized and extensively characterized in order to compare the effects of the BN-bond positioning relative to the polymer chain. In the fourth and final chapter, 1,2-azaborine-containing phosphine ligands featuring a P-B bond are synthesized. A comparative electronic structure analysis is performed between the BN-phosphine ligands and their direct all-carbon counterparts.
일반주제명Organic chemistry.
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