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Rui Feng Li Zhang Huapeng Ruan Yue Zhao Gengwen Tan Xinping Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(18):6145-6149
The first main‐group element radical based one‐dimensional magnetic chain ( 1K )n was realized by one‐electron reduction of the pyridinyl functionalized borane 1 with elemental potassium in THF in the absence of 18‐crown‐6 (18‐c‐6). The electron spin density of ( 1K )n mainly resides at the boron centers with a considerable contribution from central benzene and pyridine moieties. The spin centers exhibit an antiferromagnetic interaction as demonstrated by magnetic measurements and theoretical calculations. In contrast, the reduction in the presence of 18‐c‐6 afforded the separated radical anion salt 1K(Crown) , in which the potassium cation was trapped by THF and 18‐c‐6 molecules. Further one‐electron reduction of 1K(Crown) and ( 1K )n led to the diamagnetic monomer and polymer, respectively. 相似文献
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Dr. Andong Zhang Prof. Dr. Wei Jiang Prof. Dr. Zhaohui Wang 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(2):762-767
The first example of a two-state (neutral and reduced), stable electron-accepting material and its radical anion is presented. FV-PDI, generated from cyclocarbonylation and then a carbonyl coupling reaction, shows a largely degenerate LUMO of −4.38 eV based on the delocalization of π-electrons across the whole molecular skeleton through a fulvalene bridge. The stability and electron affinity allow spontaneous electron transfer to afford a stable radical anion. Spectroscopic characterization and structural elucidation showed that the radical anion [FV-PDI].− has remarkable stability and near-infrared absorptions extending to 1200 nm. Single-crystal X-ray diffraction analyses revealed significant changes in the molecular shape and packing arrangement of the formed radical anion. The central C−C bond linking the two PDI halves is lengthened from approximately 1.33 to 1.43 Å, and the alternating arrangement of positively and negatively charged units favor the stable charge-transfer complex. 相似文献
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《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(51):16457-16460
A supramolecular complex that can be selectively reduced to radical anions in situ by facultative anaerobic bacteria is reported. To this end, a water‐soluble bifunctional monomer bearing perylene diimide was synthesized, and its supramolecular complex with cucurbit[7]uril was fabricated on the basis of host–guest complexation, which could be reduced to forming radical anions in the presence of E. coli . It was found that this supramolecular complex could display different ability of generating radical anions by facultative anaerobic and aerobic bacteria in terms of their various reductive abilities. The selective antibacterial activity of the supramolecular complex could be realized by the photothermal performance of the radical anions under near‐infrared irradiation. It is anticipated that this method may lead to a novel bacteria‐responsive photothermal therapy to regulate balance of bacterial flora. 相似文献
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