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Facile synthesis and anion binding studies of fluorescein/benzo-12-crown-4 ether based bis-dipyrromethane (DPM) receptors
Ist Teil von
RSC advances, 2023-10, Vol.13 (43), p.342-3428
Ort / Verlag
Cambridge: Royal Society of Chemistry
Erscheinungsjahr
2023
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
Two novel fluorescein as well as benzo-12-crown-4 ether functionalized dipyrromethane receptors (
DPM3
and
DPM4
) have successfully been synthesized. The anion (used as their TBA salts) binding studies of thus prepared
DPM3
and
DPM4
receptors were evaluated by the UV-visible spectrophotometric titrations. Binding affinities as well as the stoichiometry were determined through the UV-visible titrations data with the involvement of the BindFit (v0.5) package available online at
https://supramolecular.org
. Moreover, binding events were validated by means of the comparison of the partial
1
H-NMR spectrum of the simple host molecule with that of the host-guest complex, and the 1 : 1 stoichiometry were further confirmed by the Job's method of continuous variation. From the results, we observed the binding constant (
K
a
) values of
DPM3/DPM4
with various tested anions in the range of 516.07 M
−1
to 63789.81 M
−1
, depending upon the nature/shape/size of the anions. Moreover, the anion-π interactions were confirmed by the partial
1
H-NMR spectral data, and further supported by the literature reported systems. The authors hope that such types of valued receptors will be benefitted in future for the recognizing/binding of a variety of biologically important anions.
Two novel fluorescein as well as benzo-12-crown-4 ether functionalized dipyrromethane receptors (
DPM3
and
DPM4
) have successfully been synthesized.