Synthesis of fluorinated oxygen- and sulfur-containing heteroaromatics
dc.contributor.author | Leary, Eileen M. | |
dc.contributor.author | Jones, David J. | |
dc.contributor.author | O'Donovan, Fiona P. | |
dc.contributor.author | O'Sullivan, Timothy P. | |
dc.contributor.funder | Irish Research Council | en |
dc.contributor.funder | University College Cork | en |
dc.date.accessioned | 2017-06-20T15:36:58Z | |
dc.date.available | 2017-06-20T15:36:58Z | |
dc.date.issued | 2015-06-11 | |
dc.date.updated | 2017-06-20T11:03:21Z | |
dc.description.abstract | Milk protein concentrate (79% protein) reconstituted at 13.5% (w/v) protein was heated (90 °C, 25 min, pH 7.2) with or without added calcium chloride. After fractionation of the casein and whey protein aggregates by fast protein liquid chromatography, the heat stability (90 °C, up to 1 h) of the fractions (0.25%, w/v, protein) was assessed. The heat-induced aggregates were composed of whey protein and casein, in whey protein:casein ratios ranging from 1:0.5 to 1:9. The heat stability was positively correlated with the casein concentration in the samples. The samples containing the highest proportion of caseins were the most heat-stable, and close to 100% (w/w) of the aggregates were recovered post-heat treatment in the supernatant of such samples (centrifugation for 30 min at 10,000 × g). κ-Casein appeared to act as a chaperone controlling the aggregation of whey proteins, and this effect was stronger in the presence of αS- and β-casein. | en |
dc.description.sponsorship | University College Cork (Strategic Research Fund) | en |
dc.description.status | Peer reviewed | en |
dc.description.version | Accepted Version | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.citation | O’Leary, E. M., Jones, D. J., O’Donovan, F. P. and O'Sullivan, T. P. (2015) 'Synthesis of fluorinated oxygen- and sulfur-containing heteroaromatics', Journal of Fluorine Chemistry, 176, pp. 93-120. doi: 10.1016/j.jfluchem.2015.06.002 | en |
dc.identifier.doi | doi:10.1016/j.jfluchem.2015.06.002 | |
dc.identifier.endpage | 120 | en |
dc.identifier.issn | 0022-1139 | |
dc.identifier.journaltitle | Journal of Fluorine Chemistry | en |
dc.identifier.startpage | 93 | en |
dc.identifier.uri | https://hdl.handle.net/10468/4118 | |
dc.identifier.volume | 176 | en |
dc.language.iso | en | en |
dc.publisher | Elsevier | en |
dc.rights | © 2015 Elsevier B.V. This manuscript version is made available under the CC-BY-NC-ND 4.0 license | en |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Organofluorine chemistry | en |
dc.subject | Fluorobenzofurans | en |
dc.subject | Fluoropyrones | en |
dc.subject | Fluorocoumarins | en |
dc.subject | Fluoroflavones | en |
dc.subject | Fluorochromones | en |
dc.subject | Fluoroxanthones | en |
dc.subject | Fluorothiophenes | en |
dc.subject | Fluorobenzothiophenes | en |
dc.title | Synthesis of fluorinated oxygen- and sulfur-containing heteroaromatics | en |
dc.type | Article (peer-reviewed) | en |
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