Abstract

This M.S. Thesis research objective is designed towards the racemic synthesis of a novel diastereoselectively pure, sterically bulky, cyclopropyl-containing, N-heterocyclic carbene (NHC) ligand. It is hypothesized that introduction of the sterically bulky cyclopropyl moiety at the N-substituent position of the imidazolium backbone will cause the self-assembly to develop a well defined C2-symmetric N-heterocyclic ligand, thereby limiting the free rotation about the C-N bond and creating a well-defined chiral pocket. It was discovered through utilizing classic synthetic methods that a diastereomeric imidazolium salt product was yielded, which can be attributed to the racemic synthesis of a diastereomeric cyclopropane starting material.

Library of Congress Subject Headings

Catalysts--Synthesis; Ligands--Synthesis; Carbenes (Methylene compounds); Asymmetric synthesis; Enantioselective catalysis

Publication Date

12-2014

Document Type

Thesis

Student Type

Graduate

Degree Name

Chemistry (MS)

Department, Program, or Center

School of Chemistry and Materials Science (COS)

Advisor

Michael Coleman

Advisor/Committee Member

Thomas Smith

Advisor/Committee Member

Matthew Lynn

Comments

Physical copy available from RIT's Wallace Library at QD501 .M55 2015

Campus

RIT – Main Campus

Plan Codes

CHEM-MS

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