Single-molecule conductance of a B−N substituted phenanthrene derivative and its isoelectronic CC counterpart was investigated by the scanning tunneling microscopy break junction (STM-BJ) technique. The incorporation of the B−N motif results in a better single-molecule conductivity than the CC analogue. Furthermore, the Lewis acid−base reaction between F − and the B atom of the B−N motif leads to a decrease of the conductance of the BN derivative, which can be understood due to the shifting of the energy positions of the LUMO, as revealed by quantum transport calculations, even though the HOMO−LUMO gap decreases in the B−F Lewis acid−base. These findings provide insights for modulating electron transport properties by isoelectronic structure design. The B−N isoelectronic substituted structure could be a feasible way to design single-molecule devices such as switches and chemical sensors.
The outer membrane cytochrome OmcA functions as a terminal metal reductase in the dissimilatory metal-reducing bacterium Shewanella oneidensis MR-1. The ten-heme centers shuttle electrons from the transmembrane donor complex to extracellular electron acceptors. Here, the crystallization and preliminary crystallographic analysis of OmcA are reported. Crystals of OmcA were grown by the sitting-drop vapor-diffusion method using PEG 20 000 as a precipitant. The OmcA crystals belonged to space group P2 1 , with unit-cell parameters a = 93.0, b = 246.0, c = 136.6 Å , = 90, = 97.8, = 90 . X-ray diffraction data were collected to a maximum resolution of 3.25 Å .
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