The reactions of ethylene glycol on Mo(110) were
studied using temperature-programmed reaction, infrared
reflection absorption, high-resolution electron energy loss, and X-ray
photoelectron spectroscopies. The major reaction
pathway is double C−O bond scission to evolve gas-phase ethylene at
350 and 390 K. Both X-ray photoelectron
and infrared spectra demonstrate the existence of two surface
intermediates, a bidentate
(−OCH2CH2O−) and a
monodentate (−OCH2CH2OH) species,
at saturation coverage of ethylene glycol. We demonstrate that all
ethylene
glycol in the mixed overlayer of mono- and bidentate species reacts via
a bidentate surface intermediate. Furthermore,
in contrast to previous studies on other surfaces, the dialkoxide
ethylene glycol intermediate is shown to be more
reactive than similar monoalkoxides on Mo(110). Finally,
analysis of the infrared spectra demonstrates that the
bidentate species adsorbs with C
2 (or lower)
symmetry at 300 K.
The stability constants of the promising ligand calix[4]arene-1,3-crown-6 and divalent metals of radiopharmaceutical interest: lead, barium, and strontium, were determined via NMR and UV/Vis techniques.
Two sets of functionalised calix[4]arenes, either with a 1,3-crown ether bridge or with an open-chain oligo ether moiety in 1,3-position were prepared and further equipped with additional deprotonisable sulfonamide groups to establish chelating systems for selected cations Sr2+, Ba2+, and Pb2+ ions. To improve the complexation behaviour towards these cations, calix[4]arenes with oligo ether groups and modified crowns of different sizes were synthesized. Association constants were determined by UV/Vis titration in acetonitrile using the respective perchlorate salts and logK values between 3.2 and 8.0 were obtained. These findings were supported by the calculation of the binding energies exemplarily for selected complexes with Ba2+.
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