Mary Rodgers

Professor

Wayne State University

United States

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Mary Rodgers is a Professor at Wayne State University in the United States. Her research interests include the structural and energetic properties of nucleosides and their protonated forms, with a focus on protonation-induced tautomerization and glycosidic bond stability. She has contributed to the understanding of base pairing energies in nucleoside analogues and the implications for i-motif structures relevant to DNA nanotechnology. Her recent publications explore various modifications to nucleosides and their effects on molecular interactions and stability.

Articles (13)

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2025

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2024

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2024

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2023

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2022

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2022

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2021

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2021

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2021

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2021

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2020

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2020

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2020

Collaborators (2)

E. Israel

Wayne State University

UNITED STATES

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Harrison Roy

Wayne State University

UNITED STATES

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Mary Rodgers

Research Interests

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Articles (13)

Structural and Energetic Effects of the 2-Amino and 2′- and 3′-Hydroxy Substituents of Protonated Guanosine Nucleosides: IRMPD, ER-CID, and Theoretical Studies of Protonated Guanosine and Inosine Nucleosides

Protonation-Induced Tautomerization Lowers the Activation Barriers for N-Glycosidic Bond Cleavage of Thymidine and 5-Methyluridine

Influence of 5-fluorination on the structure and glycosidic bond stability of the protonated canonical DNA and RNA cytidine nucleosides: Oh, what a difference the 2′-hydroxy substituent makes?

Influence of 2′-Modifications (O-Methylation, Fluorination, and Stereochemical Inversion) on the Base Pairing Energies of Protonated Cytidine Nucleoside Analogue Base Pairs: Implications for the Stabilities of i-Motif Structures

5-Halogenation of Uridine Suppresses Protonation-Induced Tautomerization and Enhances Glycosidic Bond Stability of Protonated Uridine: Investigations via IRMPD Action Spectroscopy, ER-CID Experiments, and Theoretical Calculations

Influence of 5-Halogenation on the Base-Pairing Energies of Protonated Cytidine Nucleoside Analogue Base Pairs: Implications for the Stabilities of Synthetic i-Motif Structures for DNA Nanotechnology Applications

Influence of 5-Methylation and the 2′- and 3′-Hydroxy Substituents on the Base Pairing Energies of Protonated Cytidine Nucleoside Analogue Base Pairs: Implications for the Stabilities of i-Motif Structures

1-Alkyl-3-methylimidazolium cation binding preferences in hexafluorophosphate ionic liquid clusters determined using competitive TCID measurements and theoretical calculations

Nature and strength of intrinsic cation–anion interactions of 1-alkyl-3-methylimidazolium hexafluorophosphate clusters

Infrared multiple photon dissociation action spectroscopy of protonated unsymmetrical dimethylhydrazine and proton-bound dimers of hydrazine and unsymmetrical dimethylhydrazine

Absolute Trends and Accurate and Precise Gas-Phase Binding Energies of 1-Alkyl-3-Methylimidazolium Tetrafluoroborate Ionic Liquid Clusters from Combined Independent and Competitive TCID Measurements

Gas-Phase Binding Energies and Dissociation Dynamics of 1-Alkyl-3-Methylimidazolium Tetrafluoroborate Ionic Liquid Clusters

Influence of the local environment on the intrinsic structures of gas-phase cytidine-5′-monophosphates

Collaborators (2)

E. Israel

Harrison Roy

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