{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,20]],"date-time":"2025-10-20T00:39:11Z","timestamp":1760920751410,"version":"build-2065373602"},"reference-count":23,"publisher":"Wiley","issue":"18","license":[{"start":{"date-parts":[[2005,11,4]],"date-time":"2005-11-04T00:00:00Z","timestamp":1131062400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J of Separation Science"],"published-print":{"date-parts":[[2005,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>The enantiomers of 1\u2010(\u03b1\u2010aminobenzyl)\u20102\u2010naphthol and 2\u2010(\u03b1\u2010aminobenzyl)\u20101\u2010naphthol analogs were separated isothermally on a cellulose\u2010<jats:italic>tris<\/jats:italic>\u20103,5\u2010dimethylphenyl carbamate\u2010based chiral stationary phase (Chiralcel OD\u2010H), at 10\u00b0C increments in the range of 5\u201335\u00b0C, using <jats:italic>n<\/jats:italic>\u2010hexane\/2\u2010propanol\/diethylamine as mobile phase. The mobile phase composition and temperature were varied to achieve baseline resolutions in a single chromatographic run. The dependence of the natural logarithms of selectivity factors, ln \u03b1, on the inverse of temperature, 1\/<jats:italic>T<\/jats:italic>, was used to determine the thermodynamic data of the enantiomers. The thermodynamic data revealed that all the compounds in this study separate <jats:italic>via<\/jats:italic> the same enthalpy\u2010driven chiral recognition mechanism.<\/jats:p>","DOI":"10.1002\/jssc.200500138","type":"journal-article","created":{"date-parts":[[2005,11,16]],"date-time":"2005-11-16T09:54:53Z","timestamp":1132134893000},"page":"2505-2510","source":"Crossref","is-referenced-by-count":15,"title":["Structural and temperature effects in the high\u2010performance liquid chromatographic enantioseparation of 1\u2010(\u03b1\u2010aminobenzyl)\u20102\u2010naphthol and 2\u2010(\u03b1\u2010aminobenzyl)\u20101\u2010naphthol analogs"],"prefix":"10.1002","volume":"28","author":[{"given":"Anita","family":"Sztojkov\u2010Ivanov","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Istv\u00e1n","family":"Szatm\u00e1ri","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Antal","family":"P\u00e9ter","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ferenc","family":"F\u00fcl\u00f6p","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2005,12,7]]},"reference":[{"key":"e_1_2_1_2_2","first-page":"381","volume":"1","author":"Betti M.","year":"1941","journal-title":"Org. 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