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. 2017 Mar 24;409(14):3695–3706. doi: 10.1007/s00216-017-0313-y

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© The Author(s) 2017

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

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Fig. 3 — Separation of acenaphthenol enantiomers under HPLC conditions using β-CD additive to binary mobile phase composed of acetonitrile:water (35:65, v/v) using C-18 (a1) and C-30 (b1) stationary phases (both 15 cm long columns; mobile phase flow 0.5 mL/min) at different temperatures and corresponding peak integration results (a2, b2; peak areas for separated enantiomers were summarized). Graph inserted within plot a2 refers to acenaphthenol peak area data obtained on Supelcosil LC-18 column (10 cm, flow 1 mL/min) without and with β-cyclodextrin additive (labeled as empty circles and black dots, respectively)