Complex mixtures can be ionized directly from paper for quantitative mass spectrometric analysis of trace components. Prior separations are an option.

Synthetic biology based on bacteria has been displayed in antitumor therapy and shown good performance. In this study, an engineered bacterium Escherichia coli MG1655 is designed with NDH‐2 enzyme (respiratory chain enzyme II) overexpression (Ec‐pE), which can colonize in tumor regions and increase localized H2O2 generation. Following from this, magnetic Fe3O4 nanoparticles are covalently linked to bacteria to act as a catalyst for a Fenton‐like reaction, which converts H2O2 to toxic hydroxyl radicals (•OH) for tumor therapy. In this constructed bioreactor, the Fenton‐like reaction occurs with sustainably synthesized H2O2 produced by engineered bacteria, and severe tumor apoptosis is induced via the produced toxic •OH. These results show that this bioreactor can achieve effective tumor colonization, and realize a self‐supplied therapeutic Fenton‐like reaction without additional H2O2 provision.

The effect of ZnO on the crystal structure, sintering behavior, and electrical conductivity of yttrium‐doped BaCeO3–BaZrO3 was investigated by unfixing or fixing the yttrium content noted as BaCe0.5Zr0.3Y0.2−xZnxO2.9−0.5x and BaCe0.5Zr0.3Y0.2O2.9+yZnO, respectively. Studies on the two series revealed that BaO·ZnO eutectic, rather than ZnO, was responsible for the sintering densification. For BaCe0.5Zr0.3Y0.2−xZnxO2.9−0.5x, the evaporation of ZnO·BaO eutectic was observed after sintering at 1300°C for 10 h, and few impurities were detected by XRD with x<0.20. For BaCe0.5Zr0.3Y0.2O2.9+yZnO, the concomitant loss of BaO with ZnO caused A‐site deficiency and led to impurities of Y2O3 for y=0.08 and 0.14, and Y2BaZnO5 for y=0.20 during the sintering. For both series, ZnO enhanced the relative density, which was above 97% with x or y varying from 0.02 to 0.08. Energy‐dispersive X‐ray spectroscopy analysis revealed that ZnO hardly entered the perovskite phase. The conductivity study also suggested that ZnO did not serve as a dopant and that yttrium content was essential for sustaining a high ionic conduction. Excessive ZnO was especially detrimental to the grain boundary conduction and thus lowered the total electrical conduction. The optimized composition of BaCe0.5Zr0.3Y0.2O2.9+0.04ZnO has been obtained, with both a high relative density (∼98.5%) and a high electrical conductivity (1.35 × 10−2 S/cm at 600°C).

Rhodium(III)-catalyzed C-H activation of heteroarenes and functionalization with bifunctional substrates such as anthranils allows facile construction of quinoline-fused heterocycles under redox-neutral conditions. The couplings feature broad substrate scope and provide step-economical access to two classes of quinoline-fused condensed heterocycles.

Homocoupling of weakly coordinating sulfoxonium ylides was accomplished via ruthenium (II) catalyzed C−H activation process. This strategy provides a convenient, efficient and step‐economic method to access 3‐substituted isocoumarins with good functional group tolerance. The sulfoxonium ylide acts both as the convenient aromatic substrate and the acylmethylation reagent in this transformation. Moreover, the products could be transformed to diverse valuable derivatives.magnified image

In article number https://doi.org/10.1002/adma.201808278, Xian‐Zheng Zhang and co‐workers develop an integrative bioreactor based on engineered bacteria for tumor therapy. This bioreactor displays bacterial tumor tropism and spontaneously supplies localized H2O2 for a therapeutic Fenton‐like reaction, achieving precise and long‐term tumor therapy.

In this study, a facile and efficient method to synthesize monofluoroalkenes by photoredox catalytic defluorinative alkylation of gem-difluoroalkenes with 4-alkyl-1,4-dihydropyridines under mild conditions (room temperature) is described. This novel strategy is applicable for a broad range of gem-difluoroalkene substrates with good functional group tolerance and a variety of 4-alkyl-1,4-dihydropyridines (including primary, secondary, and even tertiary alkyl radicals). Moreover, it also allows the challenging radical coupling with glycosyl-based 4-alkyl-1,4-dihydropyridines (DHPs) to synthesize monofluoroalkenylated saccharides.

An efficient synthesis of substituted benzenes via a base-catalyzed [3 + 3] aerobic oxidative aromatization of α,β-unsaturated carbonyl compounds with dimethyl glutaconate was reported. All the reactions were carried out under mild, metal-free conditions to afford the products in high to excellent yields with molecular oxygen as the sole oxidant and water as the sole byproduct. Furthermore, a more convenient tandem [3 + 2 + 1] aerobic oxidative aromatization reaction was developed through the in situ generation of the α,β-unsaturated carbonyl compounds from aldehydes and ketones.