Matthew K. Kiesewetter
Affiliations: | 2013- | Chemistry | University of Rhode Island, Providence, RI, United States |
Area:
Organic Chemistry, Catalysis, PolymersWebsite:
http://www.chm.uri.edu/chemsite2013/index.php?email=mkiesewetter&dest=facpage&back=Faculty%20and%20Research&this=index.php?dest=facres&button=facresGoogle:
"Matthew Kiesewetter"Bio:
http://www.chm.uri.edu/mkiesewetter/mkiesewetter_cv.pdf
http://searchworks.stanford.edu/view/8788896
Mean distance: 7.31
Parents
Sign in to add mentor| Robert M. Waymouth | grad student | 2010 | Stanford | |
| (Mechanistic insights towards new reactions and materials) | ||||
| Timothy M. Swager | post-doc | 2010-2013 | MIT | |
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Publications
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| Dharmaratne NU, Pothupitiya JU, Kiesewetter MK. (2019) The mechanistic duality of (thio)urea organocatalysts for ring-opening polymerization. Organic & Biomolecular Chemistry |
| Hewawasam RS, Kalana ULDI, Dharmaratne NU, et al. (2019) Bisurea and Bisthiourea H-Bonding Organocatalysts for Ring-Opening Polymerization: Cues for the Catalyst Design Macromolecules. 52: 9232-9237 |
| Coderre DN, Fastnacht KV, Wright TJ, et al. (2018) H-Bonding Organocatalysts for Ring-Opening Polymerization at Elevated Temperatures Macromolecules. 51: 10121-10126 |
| Pothupitiya JU, Hewawasam RS, Kiesewetter MK. (2018) Urea and Thiourea H-Bond Donating Catalysts for Ring-Opening Polymerization: Mechanistic Insights via (Non)linear Free Energy Relationships Macromolecules. 51: 3203-3211 |
| Bannin TJ, Datta PP, Kiesewetter ET, et al. (2018) Synthesizing Stilbene by Olefin Metathesis Reaction Using Guided Inquiry To Compare and Contrast Wittig and Metathesis Methodologies Journal of Chemical Education. 96: 143-147 |
| Dharmaratne NU, Pothupitiya JU, Bannin TJ, et al. (2017) Triclocarban: Commercial Antibacterial and Highly Effective H-Bond Donating Catalyst for Ring-Opening Polymerization Acs Macro Letters. 6: 421-425 |
| Pothupitiya JU, Dharmaratne NU, Jouaneh TMM, et al. (2017) H-Bonding Organocatalysts for the Living, Solvent-Free Ring-Opening Polymerization of Lactones: Toward an All-Lactones, All-Conditions Approach Macromolecules. 50: 8948-8954 |
| Datta PP, Pothupitiya JU, Kiesewetter ET, et al. (2017) Coupled equilibria in H-bond donating ring-opening polymerization: The effective catalyst-determined shift of a polymerization equilibrium European Polymer Journal. 95: 671-677 |
| Datta PP, Kiesewetter MK. (2016) Controlled Organocatalytic Ring-Opening Polymerization of ε-Thionocaprolactone. Macromolecules. 49: 774-780 |
| Fastnacht KV, Spink SS, Dharmaratne NU, et al. (2016) Bis- and Tris-Urea H-Bond Donors for Ring-Opening Polymerization: Unprecedented Activity and Control from an Organocatalyst Acs Macro Letters. 5: 982-986 |