Explore the words cloud of the STEREOPOL project. It provides you a very rough idea of what is the project "STEREOPOL" about.
The following table provides information about the project.
Coordinator |
THE UNIVERSITY OF BIRMINGHAM
Organization address contact info |
Coordinator Country | United Kingdom [UK] |
Project website | https://www.dovegrouplab.com/ |
Total cost | 2˙074˙731 € |
EC max contribution | 2˙074˙731 € (100%) |
Programme |
1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC)) |
Code Call | ERC-2015-CoG |
Funding Scheme | ERC-COG |
Starting year | 2016 |
Duration (year-month-day) | from 2016-09-01 to 2021-08-31 |
Take a look of project's partnership.
# | ||||
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1 | THE UNIVERSITY OF BIRMINGHAM | UK (BIRMINGHAM) | coordinator | 1˙621˙878.00 |
2 | THE UNIVERSITY OF WARWICK | UK (COVENTRY) | participant | 452˙852.00 |
Nature has evolved the ability to create large and complex molecules in which the 3-dimensional orientation of the atoms is critical to their performance. The essential nature of stereochemistry to the structure, and hence performance, of biopolymers makes it reasonable to expect such aspects of synthetic materials to be equally important. This area has however received little study, which is partially a consequence of the significant challenges of creating large macromolecules with well-defined stereochemistry at each repeat unit. This proposal is inspired by nature, to design polymers with exquisite structural control in which the behaviour and properties of the resultant materials will be dependent on their stereochemistry. Specifically, it will address the limitations in synthetic methodology for creating complex, functional stereocontrolled polymers and demonstrate the true potential of harnessing polymer materials with controlled stereochemistry. We will achieve this by focussing on the development of new methodologies for stereocontrolled ring-opening polymerisation of cyclic esters such that we will be able to readily access stereoregular, functional polymers, including achieving unique sequence controlled materials. While one focus will be on utilising renewable resources and green polymer synthesis methodologies, we will also take the first steps to demonstrating the utility of these novel materials by investigating the effects of stereochemistry on the bulk properties of materials as well as its ability to drive crystallisation-driven self-assembly and stereo-responsive nanoparticle behaviour for delivery applications. Achieving these goals promises to take polymers into the 3rd dimension and lead to significant technological breakthroughs in nanotechnology, medicine and sustainable materials among other areas of key future technological importance.
year | authors and title | journal | last update |
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2018 |
Laura J. Macdougall, Katherine L. Wiley, April M. Kloxin, Andrew P. Dove Design of synthetic extracellular matrices for probing breast cancer cell growth using robust cyctocompatible nucleophilic thiol-yne addition chemistry published pages: 435-447, ISSN: 0142-9612, DOI: 10.1016/j.biomaterials.2018.04.046 |
Biomaterials 178 | 2020-04-15 |
2019 |
Connor J. Stubbs, Joshua C. Worch, Hannah Prydderch, Matthew L. Becker, Andrew P. Dove Unsaturated Poly(ester-urethanes) with Stereochemically Dependent Thermomechanical Properties published pages: 174-181, ISSN: 0024-9297, DOI: 10.1021/acs.macromol.9b01700 |
Macromolecules 53/1 | 2020-04-15 |
2017 |
Guillaume Hedir, Christopher Stubbs, Phillip Aston, Andrew P. Dove, Matthew I. Gibson Synthesis of Degradable Poly(vinyl alcohol) by Radical Ring-Opening Copolymerization and Ice Recrystallization Inhibition Activity published pages: 1404-1408, ISSN: 2161-1653, DOI: 10.1021/acsmacrolett.7b00905 |
ACS Macro Letters 6/12 | 2020-04-15 |
2019 |
Yunxiang He, Jean-Charles Eloi, Robert L. Harniman, Robert M. Richardson, George R. Whittell, Robert T. Mathers, Andrew P. Dove, Rachel K. O’Reilly, Ian Manners Uniform Biodegradable Fiber-Like Micelles and Block Comicelles via “Living†Crystallization-Driven Self-Assembly of Poly( l -lactide) Block Copolymers: The Importance of Reducing Unimer Self-Nucleation via Hydrogen Bond Disruption published pages: 19088-19098, ISSN: 0002-7863, DOI: 10.1021/jacs.9b09885 |
Journal of the American Chemical Society 141/48 | 2020-04-15 |
2018 |
Maria C. Arno, Ruairà P. Brannigan, Gina M. Policastro, Matthew L. Becker, Andrew P. Dove pH-Responsive, Functionalizable Spyrocyclic Polycarbonate: A Versatile Platform for Biocompatible Nanoparticles published pages: 3427-3434, ISSN: 1525-7797, DOI: 10.1021/acs.biomac.8b00744 |
Biomacromolecules 19/8 | 2020-04-15 |
2017 |
Laura J. Macdougall, Maria M. Pérez-Madrigal, Maria C. Arno, Andrew P. Dove Nonswelling Thiol–Yne Cross-Linked Hydrogel Materials as Cytocompatible Soft Tissue Scaffolds published pages: 1378-1388, ISSN: 1525-7797, DOI: 10.1021/acs.biomac.7b01204 |
Biomacromolecules 19/5 | 2020-04-15 |
2018 |
Laura J. Macdougall, Maria M. Pérez-Madrigal, Joshua E. Shaw, Maria Inam, Judith A. Hoyland, Rachel O\'Reilly, Stephen M. Richardson, Andrew P. Dove Self-healing, stretchable and robust interpenetrating network hydrogels published pages: 2932-2937, ISSN: 2047-4830, DOI: 10.1039/c8bm00872h |
Biomaterials Science 6/11 | 2020-04-15 |
2020 |
Maria C. Arno, Maria Inam, Andrew C. Weems, Zehua Li, Abbie L. A. Binch, Christopher I. Platt, Stephen M. Richardson, Judith A. Hoyland, Andrew P. Dove, Rachel K. O’Reilly Exploiting the role of nanoparticle shape in enhancing hydrogel adhesive and mechanical properties published pages: , ISSN: 2041-1723, DOI: 10.1038/s41467-020-15206-y |
Nature Communications 11/1 | 2020-04-15 |
2018 |
Beste Orhan, Mathieu J.-L. Tschan, Anne-Laure Wirotius, Andrew P. Dove, Olivier Coulembier, Daniel Taton Isoselective Ring-Opening Polymerization of rac -Lactide from Chiral Takemoto’s Organocatalysts: Elucidation of Stereocontrol published pages: 1413-1419, ISSN: 2161-1653, DOI: 10.1021/acsmacrolett.8b00852 |
ACS Macro Letters 7/12 | 2020-04-15 |
2019 |
Joshua C. Worch, Hannah Prydderch, Sètuhn Jimaja, Panagiotis Bexis, Matthew L. Becker, Andrew P. Dove Stereochemical enhancement of polymer properties published pages: 514-535, ISSN: 2397-3358, DOI: 10.1038/s41570-019-0117-z |
Nature Reviews Chemistry 3/9 | 2020-04-15 |
2017 |
Maria Inam, Joseph R. Jones, Maria M. Pérez-Madrigal, Maria C. Arno, Andrew P. Dove, Rachel K. O’Reilly Controlling the Size of Two-Dimensional Polymer Platelets for Water-in-Water Emulsifiers published pages: 63-70, ISSN: 2374-7943, DOI: 10.1021/acscentsci.7b00436 |
ACS Central Science 4/1 | 2020-04-15 |
2017 |
Wei Yu, Maria Inam, Joseph R. Jones, Andrew P. Dove, Rachel K. O\'Reilly Understanding the CDSA of poly(lactide) containing triblock copolymers published pages: 5504-5512, ISSN: 1759-9954, DOI: 10.1039/C7PY01056G |
Polymer Chemistry 8/36 | 2019-06-18 |
2017 |
Guillaume G. Hedir, Maria C. Arno, Marvin Langlais, Jonathan T. Husband, Rachel K. O\'Reilly, Andrew P. Dove Poly(oligo(ethylene glycol) vinyl acetate)s: A Versatile Class of Thermoresponsive and Biocompatible Polymers published pages: 9178-9182, ISSN: 1433-7851, DOI: 10.1002/anie.201703763 |
Angewandte Chemie International Edition 56/31 | 2019-06-18 |
2017 |
Maria Inam, Graeme Cambridge, Anaïs Pitto-Barry, Zachary P. L. Laker, Neil R. Wilson, Robert T. Mathers, Andrew P. Dove, Rachel K. O\'Reilly 1D vs. 2D shape selectivity in the crystallization-driven self-assembly of polylactide block copolymers published pages: 4223-4230, ISSN: 2041-6520, DOI: 10.1039/C7SC00641A |
Chemical Science 8/6 | 2019-06-18 |
2017 |
Maria C. Arno, Maria Inam, Zachary Coe, Graeme Cambridge, Laura J. Macdougall, Robert Keogh, Andrew P. Dove, Rachel K. O’Reilly Precision Epitaxy for Aqueous 1D and 2D Poly(ε-caprolactone) Assemblies published pages: 16980-16985, ISSN: 0002-7863, DOI: 10.1021/jacs.7b10199 |
Journal of the American Chemical Society 139/46 | 2019-06-18 |
2017 |
Mathieu J.-L. Tschan, Nga Sze Ieong, Richard Todd, Jack Everson, Andrew P. Dove Unlocking the Potential of Poly( Ortho Ester)s: A General Catalytic Approach to the Synthesis of Surface-Erodible Materials published pages: 16664-16668, ISSN: 1433-7851, DOI: 10.1002/anie.201709934 |
Angewandte Chemie International Edition 56/52 | 2019-06-18 |
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