Chemical Vapor Transport (CVT) is a useful synthetic method for low-dimensional nanomaterials. This seminar will discuss how we’ve used it to achieve high-quality 1-D and 2-D material synthesis at high yields and larger scales than previously reported for transition metal chalcogenides and transition metal chalcohalides, and how CVT has been used for the controlled growth of several uranium and thorium chalcogenides.

Creating and curating new data appends the way we approach materials science. In additive manufacturing (AM), the fabrication of parts and objects with high complexity and high performance is advantageous over other methods. Using nanocomposites enables highly improved properties even with “commodity polymers” that do not need to undergo high-temperature processes or extensive reformulation. With artificial intelligence and machine learning (AI/ML), optimizing the formulation and manufacturing methods is possible.

Increasing CO₂ emissions into the atmosphere have led to global warming and other climate issues. One way to combat this is through the photocatalytic CO₂ reduction reaction. In this reaction, CO₂ and water are used as reactants to produce value-added products such as CO, CH₄, CH₃OH, and C₂H₅OH. TiO₂ is one of the most common photocatalysts due to its relatively high efficiency, low cost, and availability.

Photoelimination of ligands in transition metal complexes can create reactive species that can act as catalysts and reagents for several useful reactions. To better understand the dynamics of this process, the photoelimination of the ligands in the tricarbonylnitrosylcobalt complex was studied as a model for the elimination of nitrosyl ligands from mixed-ligand species.

The Nacsa Group uses electron transfer techniques to address challenges in organic synthesis. Our lab works in two main areas. The first uses electrochemistry to develop new approaches for dehydration reactions, such as the synthesis of amides and esters from carboxylic acids, with an emphasis on catalysis. Dehydrative transformations are workhorse operations in pharmaceutical R&D, but owing to the wasteful reagents overwhelmingly used to accomplish them, industry has long called for methods that avoid these reagents.

Nucleophilic dearomatization receives attention for its ability to install stereogenicity within a molecule using few steps. Whilst using aromatic substrates as a starting material can be difficult due to the low reactivity, methods have been developed to utilized them as building blocks. Exploring into pharmaceuticals and natural products will show a common moiety in di/tetrahydro pyridine and piperidines. These moieties can be synthesized via nucleophilic dearomatization of pyridines.