Nilay Hazari

Nilay Hazari's picture
Professor of Chemistry
Address: 
225 Prospect St, New Haven, CT 06511-8499
+1 (203) 432-0885

Member of Yale faculty since 2009

Research Research in the Hazari group involves synthetic inorganic and organometallic chemistry, with an emphasis on reaction mechanisms and catalysis. The long term goal of most projects is to develop homogeneous transition metal catalysts for chemical transformations, which could result in the development of more energy efficient and affordable industrial processes. Furthermore, we believe that it is important to understand reaction mechanisms, as this can play a crucial role in improving catalysts. A variety of techniques including multinuclear NMR spectroscopy, IR and UV-Visible spectroscopy, mass spectrometry, X-ray crystallography, isotopic labelling studies and computational chemistry are used to characterize compounds and investigate reaction mechanisms. In addition, the Hazari group collaborates with Professor André Taylor’s group in the Chemical and Environmental Engineering Department at Yale to incorporate small organic and organometallic molecules into Carbon Nanotubes and Organic Photovoltaics.

More specifically, projects in the group relate to: (1) the development of catalysts for the hydrogenation of carbon dioxide into formic acid and methanol and the reverse dehydrogenation of formic acid and methanol into carbon dioxide and hydrogen; (2) the design and synthesis of catalysts for the incorporation of carbon dioxide into organic molecules; (3) understanding the pathways of activation for well-defined Ni and Pd precatalysts for cross-coupling and the synthesis of new precatalysts for cross-coupling; (4) the development of small organic and organometallic molecules to dope Carbon Nanotubes for applications in electronics; and (5) the synthesis of dye molecules which can participate in Förster Resonance Energy Transfer in Organic Photovoltaics. In most of the Hazari groups’ research computational chemistry is used to support experimental observations.

Education

Postdoctoral Fellow, California Institute of Technology, 2006-2009
D.Phil. University of Oxford, 2006
M.S. University of Sydney, 2003
B.S. University of Sydney, 2002

Honors

American Chemical Society Harry Gray Award for Creative Work in Inorganic Chemistry by a Young Investigator, 2017
Arthur Greer Memorial Prize for Outstanding Scholarship by Junior Faculty Members in the Social Sciences and Sciences at Yale University, 2015
Selected as a ‘Rising Star’ by the 41st International Conference on Coordination Chemistry, 2014
Camille and Henry Dreyfus Teacher Scholar Award, 2014
Alfred P. Sloan Research Fellow, 2013
Organometallics Fellow (from the American Chemical Society JournalOrganometallics), 2012
National Science Foundation Career Award, 2012
Rhodes Scholarship for New South Wales, 2003

Recent Publications

Mohadjer Beromi, M.; Nova, A.; Balcells, D.’ Brasacchio, A. M.; Brudvig, G. W.; Guard, L. M.; Hazari, N.; Vinyard, D. J. Mechanistic Study of an Improved Ni Precatalyst for Suzuki-Miyaura Reactions of Aryl Sulfamates: Understanding the Role of Ni(I) Species. J. Am. Chem. Soc. 2017, 139, 922-936.

Goh, T.; Huang, J.-S.; Yager, K. G.; Sfeir, M. Y.; Nam, C.-Y.; Tong, X.; Guard, L. M.; Melvin, P. R.; Antonio, F.; Bartolome, B. G.; Lee, M. L.; Hazari, N.; Taylor, A. D. Quaternary Organic Solar Cells Enhanced by Co-crystalling Squaraines with Power Conversion Efficiencies >10%. Adv. Energy Mater. 2016, 6, 1600660.

Guard, L. M.; Mohadjer Beromi, M.; Brudvig, G. W.; Hazari, N.; Vinyard, D. J. Comparison of dppf-Supported Ni Precatalysts for the Suzuki-Miyaura Reaction: The Observatoin and Activity of Ni(I). Angew, Chem., Int. Ed. 2015, 54, 13352-13356.

Zhang, Y.; MacIntosh, A.; Wong, J. L.; Bielinski, E. A.; Williard, P. G.; Mercado, B. Q.; Hazari, N.; Bernskoetter, W. H. Iron Catalyzed CO2 Hydrogenation to Formate Enhanced by Lewis Acid Co-Catalysts. Chem. Sci. 2015, 6, 4291-4299.

Bielinski, E. A.; Lagaditis, P. O.; Zhang, Y.; Mercado, B. Q.; Würtele, C.; Bernskoetter, W. H.; Hazari, N.; Schneider, S. Lewis Acid Assisted Formic Acid Dehydrogenation Using a Pincer Supported Iron Catalyst. J. Am. Chem. Soc. 2014, 136, 10234-10237.

Suh, H.-W.; Guard, L. M.; Hazari, N. A Mechanistic Study of Allene Carboxylation with CO2 Resulting in the Development of a Pd(II) Pincer Complex for the Catalytic Hydroboration of CO2. Chem. Sci. 2014, 5, 3859-3872.

Hruszkewycz, D. P.; Ballcells, D.; Guard, L. M.; Hazari, N.; Tilset, M. Insight into the Efficiency of Cinnamyl Supported Precatalysts for the Suzuki-Miyaura Reaction: the Observation of Pd(I) Dimers with Bridging Allyl Ligands During Catalysis. J. Am. Chem. Soc. 2014, 136, 7300-7316.

Research Interests

Room Number: 
KCL 210