Matthew K. Kiesewetter

University of Rhode Island — United States

Materials Science · Physical Sciences

22h-index2.6kcitations47works0.02yr avg
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Research Topics

biodegradable polymer synthesis and properties(17), Carbon dioxide utilization in catalysis(17), Synthesis and Properties of Aromatic Compounds(9), Synthetic Organic Chemistry Methods(9), Advanced Polymer Synthesis and Characterization(8)

Publications47 total

Determining sulfur speciation in oxidatively crosslinked degradable polymers using sulfur <scp>K</scp>‐edge <scp>X</scp>‐ray absorption spectroscopy
Journal of Polymer Science·2024Open Access
N-Heterocyclic carbene-based gold etchants
Beilstein Journal of Nanotechnology·2023· 2 citedOpen Access
Nanoscale Carbonate Ion-Selective Amperometric/Voltammetric Probes Based on Ion–Ionophore Recognition at the Organic/Water Interface: Hidden Pieces of the Puzzle in the Nanoscale Phase
Analytical Chemistry·2023· 7 citedOpen Access
Using Surrogate Insects in Acid Bioassays for Development of New Controls for Varroa destructor (Arachnida: Varroidae)
Journal of Economic Entomology·2022Open Access
Organocatalytic ring-opening polymerization of thionolactones: anything O can do, S can do better
Polymer Chemistry·2020· 13 citedOpen Access
Bisurea and Bisthiourea H-Bonding Organocatalysts for Ring-Opening Polymerization: Cues for the Catalyst Design
Macromolecules·2019· 40 citedOpen Access
The mechanistic duality of (thio)urea organocatalysts for ring-opening polymerization
Organic & Biomolecular Chemistry·2019· 49 citedOpen Access
H-Bonding Organocatalysts for Ring-Opening Polymerization at Elevated Temperatures
Macromolecules·2018· 45 citedOpen Access
Synthesizing Stilbene by Olefin Metathesis Reaction Using Guided Inquiry To Compare and Contrast Wittig and Metathesis Methodologies
Journal of Chemical Education·2018· 17 citedOpen Access
Bifunctional and Supramolecular Organocatalysts for Polymerization
2018· 5 citedOpen Access
Quantitative Measurements of Polymer Hydrophobicity Based on Functional Group Identity and Oligomer Length
Macromolecules·2018· 48 citedOpen Access
Urea and Thiourea H-Bond Donating Catalysts for Ring-Opening Polymerization: Mechanistic Insights via (Non)linear Free Energy Relationships
Macromolecules·2018· 77 citedOpen Access
Investigations into Ring-Opening Polymerization of Functionalized ϵ-Caprolactones
Digital Commons - URI (University of Rhode Island)·2018Open Access
H-Bonding Organocatalysts for the Living, Solvent-Free Ring-Opening Polymerization of Lactones: Toward an All-Lactones, All-Conditions Approach
Macromolecules·2017· 67 citedOpen Access
Coupled equilibria in H-bond donating ring-opening polymerization: The effective catalyst-determined shift of a polymerization equilibrium
European Polymer Journal·2017· 16 citedOpen Access
Triclocarban: Commercial Antibacterial and Highly Effective H-Bond Donating Catalyst for Ring-Opening Polymerization
ACS Macro Letters·2017· 54 citedOpen Access
Bis- and Tris-Urea H-Bond Donors for Ring-Opening Polymerization: Unprecedented Activity and Control from an Organocatalyst
ACS Macro Letters·2016· 103 citedOpen Access
Controlled Organocatalytic Ring-Opening Polymerization of ε-Thionocaprolactone
Macromolecules·2016· 57 citedOpen Access
Cocatalyst Binding Effects in Organocatalytic Ring-Opening Polymerization of <scp>l</scp>-Lactide
Macromolecules·2015· 44 cited
Rate Accelerated Organocatalytic Ring-Opening Polymerization of <scp>l</scp>-Lactide via the Application of a Bis(thiourea) H-bond Donating Cocatalyst
Macromolecules·2015· 64 citedOpen Access
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Frequent Co-authors

Cheryl D. Stevenson(12), Richard C. Reiter(10), Robert M. Waymouth(9), James L. Hedrick(7), Nayanthara U. Dharmaratne(7), Partha Priya Datta(7), Elizabeth T. Kiesewetter(7), Jinal U. Pothupitiya(6), Timothy J. Bannin(4), Kurt V. Fastnacht(4), Robert G. Griffin(4), Timothy M. Swager(4), Oleg I. Kazakov(4), Justin A. Edward(3), Rukshika S. Hewawasam(3), Danielle N. Coderre(3), U. L. D. Inush Kalana(3), Rajendra Rathore(3), Steven J. Peters(3), Matthew N. Gard(3)