Representation of Molecular Structures with Persistent Homology Leads to the Discovery of Molecular Groups with Enhanced CO2 Binding

14 May 2020, Version 2
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Developing alternative strategies for efficient separation of CO2 and N2 is of general interest for the reduction of anthropogenic carbon emissions. In recent years, machine learning and high-throughput computational screening have been valuable tools in accelerated first-principles screening for the discovery of the next generation of functionalized molecules and materials. The application of machine learning for chemical applications requires the conversion of molecular structures to a machine-readable format known as a molecular representation. The choice of such representations impacts the performance and outcomes of chemical machine learning methods. Herein, we present a new concise and size-consistent molecular representation derived from persistent homology,an applied branch of mathematics. We have demonstrated its applicability in a high-throughput computational screening of a large molecular database (GDB-9) with more than 133,000 organic molecules. Our target is to identify novel molecules that selectively interact with CO2. The methodology and performance of the novel molecular fingerprinting method is presented and the new chemically-driven persistence image representation is used to screen the GDB-9 database to suggest molecules and/or functional groups with enhanced properties.

Keywords

machine Learning Applied
non-covalent interactions
High-Throughput Computational Screening

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