Suman Patra
Stanford University, Indian Association for the Cultivation of Science, IIT Guwahati
About
Dr. Suman Patra is a postdoctoral researcher in the Department of Chemistry at Stanford University, working under the mentorship of Prof. Edward I. Solomon. His research focuses on uncovering the mechanistic intricacies of non-coupled binuclear copper (NBC) enzymes, particularly tyramine β-monooxygenase (TBM), which catalyzes oxygen activation and selective C–H bond hydroxylation.His work integrates high-resolution spectroscopy, transient kinetics, and protein biochemistry to probe the formation, structure, and reactivity of short-lived copper-oxygen intermediates. As part of this effort, he performs cell culture and protein purification, enabling the isolation of active, recombinant copper enzymes for detailed spectroscopic and mechanistic studies. Through a multi-spectroscopic approach, primarily UV-Vis, CD, MCD, EXAFS, EPR, resonance Raman, and stopped-flow absorption spectroscopy, he investigates how the geometric and electronic structure of the active sites modulate reactivity and enable O₂ activation without direct Cu–Cu coupling.
Dr. Patra earned his Ph.D. in Chemistry from the Indian Association for the Cultivation of Science (IACS), Kolkata, under the supervision of Prof. Abhishek Dey, where he developed iron porphyrin-based electrocatalysts for the selective reduction of CO₂. His research emphasized mechanistic analysis using electrochemical methods coupled with in situ spectro-electrochemistry to monitor redox transitions and catalytic intermediates under applied potentials. These studies were complemented by density functional theory (DFT) calculations, which he used to model key intermediates, protonation pathways, and redox energetics, thereby providing molecular-level insight into how second-sphere interactions and ligand environments influence catalytic behaviour. His integrative experimental–computational approach provided a detailed understanding of structure-function relationships in multi-electron CO₂ reduction.
The mechanistic perspective and technical skillset developed during his doctoral work, particularly in combining spectroscopy, electrochemistry, and computation, now form the foundation of his postdoctoral research. His current studies extend those same principles to more complex metalloenzyme systems, addressing similar core questions about the role of electronic structure, metal-ligand coordination, and local environment in controlling reactivity. His long-term goal is to bridge synthetic and biological catalysis through a mechanistic lens, contributing to the development of efficient, selective systems for small-molecule activation and sustainable energy transformations.
Dr. Patra received his M.Sc. in Chemistry from the Indian Institute of Technology (IIT) Guwahati after qualifying the national IIT-JAM examination and completed his B.Sc. in Chemistry at St. Xavier’s College, Kolkata. Over the course of his academic training, he has cultivated a multidisciplinary research identity that spans coordination chemistry, spectroscopy, electrochemical catalysis, and theoretical modelling. His scientific vision centres on using spectroscopic and computational insight to guide the rational design of catalysts for environmentally relevant redox chemistry.
Employment
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Stanford University Postdoc2025 - Present
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Indian Association for the Cultivation of Science
Education
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Stanford University Postdoc2025 - Present
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Indian Association for the Cultivation of Science PhD2020 - 2025
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IIT Guwahati MSc2018 - 2020
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St. Xaviers College, Kolkata BSc2015 - 2018
Projects & Funding
Projects & funding information is unavailable.
Publications (18)
- Enhanced and selective oxygen reduction by iron porphyrin with a biguanide residue in the second coordination sphere Save
- Proton and Electron Transfer Control of Selectivity in Electrochemical CO2 Reduction: Selective Reduction of CO2 to CO, CH4, and C2H6 Catalyzed by the Same Iron Porphyrin Save
- Functional Nonheme Diiron(II) Complexes Catalyze the Direct Reduction of Nitrite to Nitric Oxide in Relevance to the Diiron Protein YtfE Save
- Electrostatic versus Hydrogen Bonding Control of Selectivity in CO2 Reduction by Iron Porphyrins Save
- Synthesis of ethane from CO 2 by a methyl transferase–inspired molecular catalyst Save
- Second sphere control of CO2 reduction selectivity by iron porphyrins: The role of spin state Save
- Reactivity of Thiolate and Hydrosulfide with a Mononuclear {FeNO}7 Complex Featuring a Very High N-O Stretching Frequency Save
- Investigation of the inherent characteristics of copper(ii) Schiff base complexes as antimicrobial agents Save
- Facile electrocatalytic proton reduction by a [Fe-Fe]-hydrogenase bio-inspired synthetic model bearing a terminal CN- ligand Save
- Kinetic isotope effect offers selectivity in CO2 reduction Save