1995
DOI: 10.1021/j100027a040
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Association of 1:1 Inclusion Complexes of Cyclodextrins into Homo- and Heterodimers: A Spectroscopic Study Using a TICT-Forming Fluorescent Probe as a Guest Compound

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Cited by 59 publications
(44 citation statements)
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“…The molar ratio [ 1 c ]/[ 1 b ] of the two complexes, obtained from the EPR spectra, increased linearly with increasing concentration of the dissolved β‐CD. When recording the EPR spectra in strongly basic solutions (pH>12.5) the signals of the 1:2 complex 1 c disappeared while those of the 1:1 complex remained (see Supporting Information), similar to what had been found previously with a pyrene‐modified γ‐CD8a and with the 1:2 complex between 4‐(dimethylamino) benzonitrile and β‐CD 8b. The lability of the 1:2 complex at high pH values is attributed to the fact that in basic media dissociation of the secondary CD hydroxy group (p K a =12.5) takes place to form an anionic species.…”
Section: Spectroscopic and Thermodynamic Parameters For CD Complex Fosupporting
confidence: 84%
“…The molar ratio [ 1 c ]/[ 1 b ] of the two complexes, obtained from the EPR spectra, increased linearly with increasing concentration of the dissolved β‐CD. When recording the EPR spectra in strongly basic solutions (pH>12.5) the signals of the 1:2 complex 1 c disappeared while those of the 1:1 complex remained (see Supporting Information), similar to what had been found previously with a pyrene‐modified γ‐CD8a and with the 1:2 complex between 4‐(dimethylamino) benzonitrile and β‐CD 8b. The lability of the 1:2 complex at high pH values is attributed to the fact that in basic media dissociation of the secondary CD hydroxy group (p K a =12.5) takes place to form an anionic species.…”
Section: Spectroscopic and Thermodynamic Parameters For CD Complex Fosupporting
confidence: 84%
“…The upward displacements of H-3 and H-5 of β-CD indicated that these protons are located near an electron cloud that induced anisotropic magnetic shielding. 43 Similar results have been described in the literature 44 as evidence of complexation.…”
Section: Tga Analysissupporting
confidence: 86%
“…8). According to the enthalpy-entropy compensation theory [31][32][33], the gain of enthalpy on the formation of inclusion compounds is achieved with the loss of entropy [34], DS1 is negative primarily due to the restricted rotation of the host and the guest in the formed complex [35]. The negative enthalpy change in these complexes reveals the presence of hydrophobic interaction [36,37] in the AFB 1 -CD systems.…”
Section: Article In Pressmentioning
confidence: 99%
“…Complexation of the cyclodextrin and either wholly or partially included guest molecules results in a number of interesting spectroscopic effects [21][22][23][24][25][26][27][28][29][30][31][32][33][34]. We have studied the solvent and complex formation effects on the fluorescence spectrum and enhancement factor of the molecule, AFB 1 in different temperatures.…”
Section: Introductionmentioning
confidence: 99%