Understanding the effects of building block rings of π electron-rich organic photocatalysts in CO2 transformation to amino acids

Understanding the effective factors in the performance of some Oligo (p-phenylenes) (OPPs) and Polycyclic Aromatic Hydrocarbons (PAHs), as efficient organocatalysts in photocatalytic CO2 transformations are the main goals of this investigation. The studies are based on density functional theory (DFT) calculations on the mechanistic aspects of C-C bond formation through a coupling reaction between CO2 center dot- and amine radical. The reaction is performed through two successive single electron transfer steps. After careful kinetic investigations by Marcus' theory rules, powerful descriptors are used to describe the behavior of observed barrier energies of electron transfer steps. The studied PAHs and OPPs consist of different numbers of rings. Thus, it can be considered different charge densities, afforded from pi electrons, of PAHs and OPPs that cause distinguished efficiency in kinetic aspects of electron transfer steps. Electrostatic Surface Potential (ESP) analyses reveal a good relationship between the charge density of the studied organocatalysts in single electron transfer (SET) steps and the kinetic parameters of the steps. Moreover, the contribution of rings in the framework of PAHs and OPPs would be another effective factor in the barrier energies of SET steps. Aromatic properties of the rings, studied by the Anisotropy of the Current-Induced Density (ACID), Nucleus-Independent Chemical Shift (NICS), the multi-center bond order (MCBO), and AV1245 Indexes, are the other impressive factors in the role of rings in SET steps. The results show that the aromatic properties of the rings are not similar to each other. Higher aromaticity affords remarkable reluctance of the corresponding ring to participate in SET steps.

Automated summary

The effective factors in the performance of Oligo (p-phenylenes) (OPPs) and Polycyclic Aromatic Hydrocarbons (PAHs) as organocatalysts in photocatalytic CO2 transformations were investigated using density functional theory calculations. The study focused on the mechanistic aspects of C-C bond formation in a coupling reaction between CO2 center dot- and amine radical. The results showed that the charge density and aromatic properties of the studied organocatalysts and rings played important roles in the kinetic aspects of the electron transfer steps.