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Hayashida, O. and Hamachi, I. (2004) Fluorophore Appended Saccharide Cyclophane: Self-Association, Fluorescent Properties, Heterodimers with Cyclodextrins, and Cross-Linking Behavior with Peanut Agglutinin of Dansyl-Modified Saccharide Cyclophane. The Journal of Organic Chemistry, 69, 3509-3516. http://dx.doi.org/10.1021/jo0496852

has been cited by the following article:

• TITLE: Synthesis of a Rhodamine-Appended Cyclophane as a Fluorescence Host in Water

  AUTHORS: Osamu Hayashida, Yu Kaku

  KEYWORDS: Host-Guest Chemistry, Water-Soluble Cyclophane, Fluorescent Sensing

  JOURNAL NAME: Advances in Chemical Engineering and Science, Vol.4 No.4, September 19, 2014

  ABSTRACT: A cationic water-soluble cyclophane (1a) having a rhodamine moiety as a red-fluorescence fluorophore was prepared by reaction of a monoamine derivative of tetraaza[6.1.6.1]paracyclophane having three N-t-butoxycarbonyl-β-alanine residues with rhodamine B isothiocyanate, followed by removal of the protecting groups. The guest-binding behavior of 1a toward anionic guests such as dabsyl derivative and 4-(1-pyrene)butanoate was investigated by fluorescence spectroscopy. The results suggested the formation of host-guest complexes with a stoichiometric ratio of 1:1 and the binding constants (K) of the host-guest complexes were evaluated.