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Steric hindrance-enforced distortion as a general strategy for the design of fluorescence "turn-on" cyanide probes
KTH, School of Biotechnology (BIO), Theoretical Chemistry and Biology.ORCID iD: 0000-0001-6508-8355
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2013 (English)In: Chemical Communications, ISSN 1359-7345, E-ISSN 1364-548X, Vol. 49, no 86, 10136-10138 p.Article in journal (Refereed) Published
Abstract [en]

For the rational design of fluorescence "turn-on" cyanide probes, a general strategy is developed by introducing a dicyanovinyl group at the sterically demanding position of a large pi framework.

Place, publisher, year, edition, pages
2013. Vol. 49, no 86, 10136-10138 p.
Keyword [en]
Intramolecular Charge-Transfer, Excimer Fluorescence, 1, 1'-Binaphthyl Scaffold, Optical-Properties, Rational Design, Anion, Chemosensor, Chemodosimeter, Viscosity, Red
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:kth:diva-133665DOI: 10.1039/c3cc46008hISI: 000325642400026Scopus ID: 2-s2.0-84885109338OAI: oai:DiVA.org:kth-133665DiVA: diva2:662782
Note

QC 20131108

Available from: 2013-11-08 Created: 2013-11-08 Last updated: 2017-12-06Bibliographically approved

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Li, Xin

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