Please use this identifier to cite or link to this item: https://doi.org/10.1021/co200136b
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dc.titleSynthesis of a novel BODIPY library and its application in the discovery of a fructose sensor
dc.contributor.authorZhai, D.
dc.contributor.authorLee, S.-C.
dc.contributor.authorVendrell, M.
dc.contributor.authorLeong, L.P.
dc.contributor.authorChang, Y.-T.
dc.date.accessioned2014-06-23T05:51:47Z
dc.date.available2014-06-23T05:51:47Z
dc.date.issued2012-02-13
dc.identifier.citationZhai, D., Lee, S.-C., Vendrell, M., Leong, L.P., Chang, Y.-T. (2012-02-13). Synthesis of a novel BODIPY library and its application in the discovery of a fructose sensor. ACS Combinatorial Science 14 (2) : 81-84. ScholarBank@NUS Repository. https://doi.org/10.1021/co200136b
dc.identifier.issn21568952
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77174
dc.description.abstractWe prepared a new library of 160 compounds by conjugation of a BODIPY core to a collection of aldehydes. This library was screened against 52 biologically relevant analytes and we identified one fluorescent sensor of fructose (Fructose Orange). Fructose Orange showed a 24-fold fluorescence increase upon recognition of fructose and an outstanding selectivity among 24 different saccharides. NMR studies confirmed that five different binding interactions were formed between the sensor and fructose. Furthermore, Fructose Orange was applied to the quantification of fructose in soft drinks, being the most selective fluorescent sensor for fructose reported to date. © 2012 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/co200136b
dc.sourceScopus
dc.subjectchemosensor
dc.subjectfluorescence
dc.subjectmolecular recognition
dc.subjectsaccharides
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/co200136b
dc.description.sourcetitleACS Combinatorial Science
dc.description.volume14
dc.description.issue2
dc.description.page81-84
dc.identifier.isiut000300116000001
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