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Spectroscopic investigation of cyclodextrin monomers,derivatives, polymers and azo dyes (1)
Authors:Miyoko Suzuki  Éva Fenyvesi  Mária Szilasi  József Szejtli  Márton Kajtár  Béla Zsadon  Yoshio Sasaki
Institution:(1) Faculty of Pharmaceutical Sciences, Osaka University, 1-6, Yamadaoka, 565 Suita, Osaka, Japan;(2) Chinoin Pharmaceutical Chemical Works, Tó u. 1-5, H-1045 Budapest, Hungary;(3) Department of Chemical Technology, Eötvös Loránd University, Muzeum krt 6-8, H-1088 Budapest, Hungary;(4) Institute of Organic Chemistry, Eötvös Loránd University, Muzeum krt 4/b, H-1088 Budapest, Hungary
Abstract:Circular dichroism (CD) and visible spectra of inclusion compounds between Methyl Orange (MO) analogues and agr-, beta-, gamma-cyclodextrin (cdx), 2,6-dimethyl-and 2,3,6-trimethyl-beta-cdx, water soluble agr-, beta-, gamma-cdx polymer products were investigated. In the CD-spectroscopic investigation, the complex with agr-cdx epichlorohydrin condensate showed a large amplitude and splitting of the induced pgr rarr pgr* band. Fractions of glyceryl ether of less than 2000 and polymer of more than 10000 dalton molecular mass were separated. Complexes of above two fractions and MO showed the same splitting spectral pattern. Job's plots from visible spectra showed the formation of the 1ratio1 complex and CD-data suggested the co-existence of the 2ratio1 MO-cdx complex. This splitting pattern showed the reversal of the signs when agr-cdx-ethyleneglycol-bis(epoxypropyl) ether was used and disappeared when larger host molecules and azo dyes were used. The splitting was explained by exciton interaction.
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