All Outputs (3)

Excited-State Aromatic Interactions in the Aggregation-Induced Emission of Molecular Rotors (2017)
Journal Article
Sturala, J., Etherington, M. K., Bismillah, A. N., Higginbotham, H. F., Trewby, W. J., Aguilar, J. A., Bromley, E. H., Avestro, A.-J., Monkman, A. P., & McGonigal, P. R. (2017). Excited-State Aromatic Interactions in the Aggregation-Induced Emission of Molecular Rotors. Journal of the American Chemical Society, 139(49), 17882-17889. https://doi.org/10.1021/jacs.7b08570

Small, apolar aromatic groups, such as phenyl rings, are commonly included in the structures of fluorophores in order to impart hindered intramolecular rotations, leading to desirable solid-state luminescence properties. However, they are not normall... Read More about Excited-State Aromatic Interactions in the Aggregation-Induced Emission of Molecular Rotors.

Construction of a chassis for a tripartite protein-based molecular motor (2017)
Journal Article
Small, L. S., Bruning, M., Thomson, A. R., Boyle, A. L., Davies, R. B., Curmi, P. M., …Bromley, E. H. (2017). Construction of a chassis for a tripartite protein-based molecular motor. ACS Synthetic Biology, 6(6), 1096-1102. https://doi.org/10.1021/acssynbio.7b00037

Improving our understanding of biological motors, both to fully comprehend their activities in vital processes, and to exploit their impressive abilities for use in bionanotechnology, is highly desirable. One means of understanding these systems is t... Read More about Construction of a chassis for a tripartite protein-based molecular motor.

Log D versus HPLC derived hydrophobicity: The development of predictive tools to aid in the rational design of bioactive peptoids (2017)
Journal Article
Bolt, H., Williams, C., Brooks, R., Zuckermann, R., Cobb, S., & Bromley, E. (2017). Log D versus HPLC derived hydrophobicity: The development of predictive tools to aid in the rational design of bioactive peptoids. Biopolymers, 108(4), Article e23014. https://doi.org/10.1002/bip.23014

Hydrophobicity has proven to be an extremely useful parameter in small molecule drug discovery programmes given that it can be used as a predictive tool to enable rational design. For larger molecules, including peptoids, where folding is possible, t... Read More about Log D versus HPLC derived hydrophobicity: The development of predictive tools to aid in the rational design of bioactive peptoids.