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Diastereo-specific conformational properties of neutral, protonated and radical cation forms of (1R, 2S)-cis- and (1R, 2R)-trans-amino-indanol by gas phase spectroscopy1. Issue 39 (21st October 2015)
Record Type:
Journal Article
Title:
Diastereo-specific conformational properties of neutral, protonated and radical cation forms of (1R, 2S)-cis- and (1R, 2R)-trans-amino-indanol by gas phase spectroscopy1. Issue 39 (21st October 2015)
Main Title:
Diastereo-specific conformational properties of neutral, protonated and radical cation forms of (1R, 2S)-cis- and (1R, 2R)-trans-amino-indanol by gas phase spectroscopy1
<abstract abstract-type="toc"> <title> <x xml:space="preserve">Abstract</x> </title> <p> <graphic position="anchor" id="ga" xlink:href="ark:/27927/pgkgntvqx6" xlink:type="simple" xmlns:xlink="http://www.w3.org/1999/xlink" />The effects of ionisation and protonation on the geometric and electronic structure of a prototypical aromatic amino-alcohol with two chiral centres are revealed by IR and UV spectroscopy.</p> </abstract>