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Jean M. McKenna

Researcher at University of Sheffield

Publications -  22
Citations -  171

Jean M. McKenna is an academic researcher from University of Sheffield. The author has contributed to research in topics: Electrophilic addition & Benzyl acetate. The author has an hindex of 7, co-authored 22 publications receiving 168 citations.

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Bis-steroids as potential enzyme models: perylene solubilisation and dye spectral changes with aqueous solutions of some derivatives of conessine and cholic acid

TL;DR: Several bis-steroids derived from conessine or cholic acid solubilise perylene into aqueous solution without evidence of micelle formation, and cause spectral changes in pinacyanol iodide; however, these effects (characteristic of hydrophobic interaction) only on micellisation or not at all as discussed by the authors.
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Ultrafast coherent control and quantum encoding of molecular vibrations in D2+ using intense laser pulses

TL;DR: In this paper, a pump-probe-type technique is proposed to manipulate the D2+ ion with ultrashort pulse sequences, which can be used to realize a vibrational qubit.
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Geometry- and diffraction-independent ionization probabilities in intense laser fields: Probing atomic ionization mechanisms with effective intensity matching

TL;DR: In this article, an experimental technique for the comparison of ionization processes in ultrafast laser pulses irrespective of pulse ellipticity is presented. And the probability of recollision ionization in a linearly polarized laser pulse is discussed in terms of the Keldysh adiabaticity parameter {gamma}, and the influence of the precursor ionic states present in recollison ionization is observed.
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The mechanism of photolysis of benzyl halides and benzyl acetate in alcohols

TL;DR: In this paper, the photolysis of benzyl chloride, bromide, iodide, and acetate in methanol and t-butyl alcohol has been examined, and also 3,5-dimethoxybenzyl chloride in ethanol.
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The mechanism of photolysis of some benzyltrimethylammonium salts in water and in alcohols

TL;DR: In this article, the photolysis of a range of benzyltrimethylammonium and 3,5-dimethoxybenzyl trimethylmonium salts in water or methanol at 253.7 nm gave typically benzyl alcohols (or benzyl methyl ethers), toluenes, bibenzyls and isomers, and di- and tri-methylammium salts.