posted on 2017-04-13, 00:00authored byNikhil S. Japtiwale
<p>C-C coupling reactions are of high interest to synthetic chemists due to their ability to accomplish chemical transformations often involving value addition to the substrates.<sup> </sup>The high impact of the research in this area is evident by a Nobel Prize awarded to Richard F. Heck, Ei-ichi Negishi, and Akira Suzuki in the year 2010. This thesis outlines a research project in the area of C-C coupling reactions to synthesize industrially relevant products using substrate molecules typically small oxygenates, such as, acetic acid, and C2-C3 aldehydes. The focus is on the development of suitable catalysts to accomplish these transformations efficiently. Self C-C coupling of acetic acid, and propionaldehyde via ketonization and aldol condensation, respectively, are the reactions under investigation during the course of this thesis project. Acetone, and 2-methyl-2-pentenal are the desired products, which have a wide range of industrial applications. However, tendency of these molecules to form longer carbon chains via continuous coupling is a major drawback during these reactions. Therefore, a catalyst that is highly selective to the desired products and that can deliver competitive yields is needed. With this regard, novel materials containing cerium and/or manganese heteroatoms incorporated in the zeolite frameworks are tested as catalysts. The data show the presence of Ce<sup>3+</sup>, and Mn<sup>3+</sup> heteroatom species in the crystalline zeolite framework, and these catalysts are active at low temperature during self-aldol condensation reaction as well as can deliver higher rates to the desired products during the C-C coupling reactions of small oxygenates tested.</p>