Nitro-Substituted Stilbeneboronate Pinacol Esters and Their Fluoro-Adducts. Fluoride Ion Induced Polarity Enhancement of Arylboronate Esters
datasetposted on 08.06.2007, 00:00 by Alexander Oehlke, Alexander A. Auer, Ina Jahre, Bernhard Walfort, Tobias Rüffer, Petra Zoufalá, Heinrich Lang, Stefan Spange
A series of stilbeneboronate pinacol cyclic esters, containing none to three nitro groups, have been synthesized by various olefination reactions and characterized by X-ray single-crystal structure analysis. A stilbeneboronate ester bearing electron-acceptor groups experiences transition to a push−pull π-electron system upon complexation with one fluoride ion at the boron atom. The UV−vis absorption maxima of the presented nitro-substituted stilbeneboronate esters are red-shifted upon addition of fluoride ions, indicating this binding event. The enhancement of the polarity of the investigated compounds and the changes in the electronic system were investigated by UV−vis absorption spectroscopy and solvatochromism. Additionally, studies were performed by natural bond orbital (NBO) analysis and RI-CC2 calculations of the vertical excitation energies. The synergism of fluoride ion complexation and solvation upon the UV−vis band shift is interpreted in terms of linear solvation energy relationships (LSERs) using the Kamlet−Taft solvent parameter set. It is found that the UV−vis absorption of the fluoro-boronates is strongly dependent on the solvents hydrogen-bond donating ability.
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absorptionnitro groupsfluoride ionsolefination reactionsstilbeneboronate pinacol cyclic estersfluoride ion complexationbinding eventUVboron atomNBOsolvation energy relationshipsexcitation energiesFluoride Ion Induced Polarity Enhancementfluoride ionArylboronate EstersA seriesLSERanalysisstilbeneboronate ester