A series of new trigonal pyramidal {SeO(OH)} bridging lanthanide-containing antimono-seleno-tungstates [HN(CH)]NaCsH[LnSeWO(OH)(HO)(SbWO)(SeWO)(SeSbWO)]·32HO [Ln = Tb (), Dy (), Ho (), Er ()] have been prepared by the synthetic strategy of simultaneously using the antimonotungstate precursor and simple material in an acidic aqueous solution and structurally characterized by single-crystal X-ray diffraction, powder X-ray diffraction, IR spectrometry, and thermogravimetric analysis. Their molecular structures contain an unprecedented hexameric polyoxoanion [LnSeWO(OH)(HO)(SbWO)(SeWO)(SeSbWO)] constituted by two equivalent trimeric subunits LnWO(HO)(SbWO)(SeWO)(SeSbWO) bridged via two μ-{SeO(OH)} linkers. Furthermore, the catalytic oxidation of various aromatic sulfides and sulfur mustard simulant 2-chloroethyl ethyl sulfide (CEES) by compound as the heterogeneous catalyst has been investigated, exhibiting high conversion and selectivity as well as good stability and recyclability.
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http://dx.doi.org/10.1021/acs.inorgchem.4c00767 | DOI Listing |
Molecules
April 2024
State Key Laboratory of Applied Organic Chemistry, College of Chemistry and Chemical Engineering, Lanzhou University, Lanzhou 730000, China.
The diselenide bond has attracted intense interest in redox-responsive drug delivery systems (DDSs) in tumor chemotherapy, due to its higher sensitivity than the most investigated bond, namely the disulfide bond. Here, a diselenide-bridged doxorubicin dimeric prodrug (D-DOX) was designed by coupling two doxorubicin molecules with a diselenodiacetic acid (DSeDAA) molecule via α-amidation, as a redox-triggered drug self-delivery system (DSDS) for tumor-specific chemotherapy. The drug release profiles indicated that the D-DOX could be cleaved to release the derivatives selenol (DOX-SeH) and seleninic acid (DOX-SeOOH) with the triggering of high GSH and HO, respectively, indicating the double-edged sword effect of the lower electronegativity of the selenide atom.
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