Research outputs
2025
Organocatalytic glycolysis of polyethylene terephthalate and product separation by membrane filtration
Sutton, J., Grause, G., Hmayed, A. A. R., Street, S. T. G., Dove, A. P., & Wood, J. (2025). Organocatalytic glycolysis of polyethylene terephthalate and product separation by membrane filtration. CHEMICAL ENGINEERING JOURNAL, 512. doi:10.1016/j.cej.2025.162400
Precision Stealth Nanofibers via PET-RAFT Polymerisation: Synthesis, Crystallization-driven Self-assembly and Cellular Uptake Studies
Street, S. T. G., Shteinberg, E., Hernandez, J. D. G., Parkin, H. C., Harniman, R. L., Willerth, S., & Manners, I. (2025). Precision Stealth Nanofibers via PET-RAFT Polymerisation: Synthesis, Crystallization-driven Self-assembly and Cellular Uptake Studies. CHEMISTRY-A EUROPEAN JOURNAL, 31(22). doi:10.1002/chem.202500108
2024
Mechanism of Action and Design of Potent Antibacterial Block Copolymer Nanoparticles
Parkin, H. C., Street, S. T. G., Gowen, B., Da-Silva-Correa, L. H., Hof, R., Buckley, H. L., & Manners, I. (2024). Mechanism of Action and Design of Potent Antibacterial Block Copolymer Nanoparticles. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 146(8), 5128-5141. doi:10.1021/jacs.3c09033
2023
Optimization of precision nanofiber micelleplexes for DNA delivery
Street, S. T. G., Parkin, H. C., Shopperly, L., Chrenek, J., Letwin, K., Willerth, S. M., & Manners, I. (2023). Optimization of precision nanofiber micelleplexes for DNA delivery. BIOMATERIALS SCIENCE, 11(10), 3512-3523. doi:10.1039/d2bm02014a
2022
Length-Controlled Nanofiber Micelleplexes as Efficient Nucleic Acid Vehicles
Street, S. T. G., Chrenek, J., Harniman, R. L., Letwin, K., Mantell, J. M., Borucu, U., . . . Manners, I. (2022). Length-Controlled Nanofiber Micelleplexes as Efficient Nucleic Acid Vehicles. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. doi:10.1021/jacs.2c06695
Structure-activity relationship studies on divalent naphthalene diimide G quadruplex ligands with anticancer and antiparasitic activity
Perez-Soto, M., Penalver, P., Street, S. T. G., Weenink, D., O'Hagan, M. P., Ramos-Soriano, J., . . . Morales, J. C. (2022). Structure-activity relationship studies on divalent naphthalene diimide G quadruplex ligands with anticancer and antiparasitic activity. BIOORGANIC & MEDICINAL CHEMISTRY, 71. doi:10.1016/j.bmc.2022.116946
Uniform, length-tunable antibacterial 1D diblock copolymer nanofibers
Parkin, H. C., Garcia-Hernandez, J. D., Street, S. T. G., Hof, R., & Manners, I. (2022). Uniform, length-tunable antibacterial 1D diblock copolymer nanofibers. POLYMER CHEMISTRY, 13(20), 2941-2949. doi:10.1039/d2py00262k
Precision polymer nanofibers with a responsive polyelectrolyte corona designed as a modular, functionalizable nanomedicine platform
Street, S. T. G., He, Y., Harniman, R. L., Garcia-Hernandez, J. D., & Manners, I. (2022). Precision polymer nanofibers with a responsive polyelectrolyte corona designed as a modular, functionalizable nanomedicine platform. POLYMER CHEMISTRY, 13(20), 3009-3025. doi:10.1039/d2py00152g
2021
Cargo Encapsulation in Uniform, Length-Tunable Aqueous Nanofibers with a Coaxial Crystalline and Amorphous Core
Garcia-Hernandez, J. D., Street, S. T. G., Kang, Y., Zhang, Y., & Manners, I. (2021). Cargo Encapsulation in Uniform, Length-Tunable Aqueous Nanofibers with a Coaxial Crystalline and Amorphous Core. MACROMOLECULES, 54(12), 5784-5796. doi:10.1021/acs.macromol.1c00672
Imide Condensation as a Strategy for the Synthesis of Core-Diversified G-Quadruplex Ligands with Anticancer and Antiparasitic Activity**
Street, S. T. G., Penalver, P., O'Hagan, M. P., Hollingworth, G. J., Morales, J. C., & Galan, M. C. (2021). Imide Condensation as a Strategy for the Synthesis of Core-Diversified G-Quadruplex Ligands with Anticancer and Antiparasitic Activity**. CHEMISTRY-A EUROPEAN JOURNAL, 27(28), 7712-7721. doi:10.1002/chem.202100040
2020
Cellular uptake and targeting of low dispersity, dual emissive, segmented block copolymer nanofibers
Street, S. T. G., He, Y., Jin, X. -H., Hodgson, L., Verkade, P., & Manners, I. (2020). Cellular uptake and targeting of low dispersity, dual emissive, segmented block copolymer nanofibers. CHEMICAL SCIENCE, 11(32), 8394-8408. doi:10.1039/d0sc02593c
2018
Extending the Scope of "Living" Crystallization-Driven Self-Assembly: Well-Defined 1D Micelles and Block Comicelles from Crystallizable Polycarbonate Block Copolymers
Finnegan, J. R., He, X., Street, S. T. G., Garcia-Hernandez, J. D., Hayward, D. W., Harniman, R. L., . . . Manners, I. (2018). Extending the Scope of "Living" Crystallization-Driven Self-Assembly: Well-Defined 1D Micelles and Block Comicelles from Crystallizable Polycarbonate Block Copolymers. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 140(49), 17127-17140. doi:10.1021/jacs.8b09861
2017
Divalent Naphthalene Diimide Ligands Display High Selectivity for the Human Telomeric G-quadruplex in K<SUP>+</SUP> Buffer
Street, S. T. G., Chin, D. N., Hollingworth, G. J., Berry, M., Morales, J. C., & Galan, M. C. (2017). Divalent Naphthalene Diimide Ligands Display High Selectivity for the Human Telomeric G-quadruplex in K<SUP>+</SUP> Buffer. CHEMISTRY-A EUROPEAN JOURNAL, 23(29), 6953-6958. doi:10.1002/chem.201700140
Is UV-Induced Electron-Driven Proton Transfer Active in a Chemically Modified A•T DNA Base Pair?
Rottger, K., Marroux, H. J. B., Chemin, A. F. M., Elsdon, E., Oliver, T. A. A., Street, S. T. G., . . . Roberts, G. M. (2017). Is UV-Induced Electron-Driven Proton Transfer Active in a Chemically Modified A•T DNA Base Pair?. JOURNAL OF PHYSICAL CHEMISTRY B, 121(17), 4448-4455. doi:10.1021/acs.jpcb.7b02679
2015
Catalytic Conversion of Ethanol to <i>n</i>-Butanol Using Ruthenium P-N Ligand Complexes
Wingad, R. L., Gates, P. J., Street, S. T. G., & Wass, D. F. (2015). Catalytic Conversion of Ethanol to <i>n</i>-Butanol Using Ruthenium P-N Ligand Complexes. ACS CATALYSIS, 5(10), 5822-5826. doi:10.1021/acscatal.5b01327
2014
A Flexible Solution to Anion Transport: Powerful Anionophores Based on a Cyclohexane Scaffold
Cooper, J. A., Street, S. T. G., & Davis, A. P. (2014). A Flexible Solution to Anion Transport: Powerful Anionophores Based on a Cyclohexane Scaffold. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 53(22), 5609-5613. doi:10.1002/anie.201311071