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Jennifer R. Hiscock

Researcher at University of Kent

Publications -  84
Citations -  2699

Jennifer R. Hiscock is an academic researcher from University of Kent. The author has contributed to research in topics: Hydrogen bond & Chemistry. The author has an hindex of 22, co-authored 67 publications receiving 2315 citations. Previous affiliations of Jennifer R. Hiscock include University of Southampton.

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Managing research throughout COVID-19: Lived experiences of supramolecular chemists

TL;DR: The international Women in Supramolecular Chemistry network believes that taking an area-specific approach effectively supports equality, diversity, and inclusion, and demonstrate that research leaders have often taken responsibility for their teams' mental health and well-being at the cost of their own as mentioned in this paper .
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Supramolecular self-associating amphiphiles: determination of molecular self-association properties and calculation of critical micelle concentration using a high-throughput, optical density based methodology.

TL;DR: In this article , the authors derived critical micelle concentration values for four supramolecular self-associating amphiphiles using the standard pendant drop approach and presented a new high-throughput, optical density measurement based methodology, to enable the estimation of critical microelle concentrations over multiple temperatures.
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Anionic Self‐Assembling Supramolecular Enhancers of Antimicrobial Efficacy against Gram‐Negative Bacteria

TL;DR: In this paper , the use of anionic supramolecular self-associating amphiphiles (SSAs) as antimicrobial efficacy enhancers for commonly used antimicrobial agents, to which there is known resistance, against Gram-negative bacteria was investigated.
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Ionicity-dependent proton-coupled electron transfer of supramolecular self-assembled electroactive heterocycles

TL;DR: The effect of self-assembly on proton-coupled electron transfer has implications for the understanding of electron transfer kinetics in aqueous organic redox flow batteries, especially at high concentration where organic-organic intermolecular interactions become dominant even for highly soluble organic species.