摘要
A biomimetic assembly of per-O-methylated-cyclodextrin dimer with cobalt proto-porphyrin (Co III -PPIX@Py2CD) was achieved via covalent linkage between Co III of Co III -PPIX and pyridine N of Py2CD (primarily synthesized by the acyl chlorination reaction of two β-CDs monomers with 3,5-bis (bromomethyl) pyridine). Ultraviolet–visible (UV–vis) and circular dichroism (CD) absorption spectroscopy , and NMR hydrogen spectroscopy (H 1 -NMR) were adopted to carefully characterize the structure of Py2CD and its functional assembly with Co III -PPIX. X-ray photoelectron spectroscopy (XPS) was employed to affirm the binding of the as-obtained Co III -PPIX@Py2CD, whose electrochemical kinetics were extensively studied to validate the feasibility in the catalytic reduction of hydrogen peroxide (H 2 O 2 ). The developed sensor displayed the wide linear range for H 2 O 2 detection and the low detection limit of 2.47 × 10 −7 M. This work sheds some constructive lights on rational design and synthesis of preeminently biomimic carrier and high cost-effectiveness catalyst for (bio)analytical applications.
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