Abstract
Nitro-substituted π-electronic molecules are fascinating because of their unique electronic and optical properties and the ease of their transformation into various functional derivatives. Herein, nitro-introduced dipyrrolyldiketone BF2 complexes as anion-responsive π-electronic molecules were synthesized, and their electronic properties and anion-binding abilities were investigated by spectroscopic analyses and theoretical studies. The obtained nitro-substituted derivatives showed solvent-dependent UV/vis spectral changes and high anion-binding affinities due to the easily pyrrole-inverted conformations and polarized pyrrole NH sites upon the introduction of electron-withdrawing moieties.
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Kuno, A., & Maeda, H. (2021). Nitro-substituted dipyrrolyldiketone bf2 complexes as electronic-state-adjustable anion-responsive π-electronic systems. Molecules, 26(3). https://doi.org/10.3390/molecules26030595
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