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Fluorinated molecules are widely used in pharmaceutical and agrochemical industries. Multifluoroalkyl-containing compounds have attracted increasing attention for their unique ability to alter the activity of drugs and bioactive molecules. Herein, we report an efficient Rh(III)-catalyzed, redox-neutral, C–H multifluoroalkenylation of benzamides with multifluoroalkenes, which provides a versatile protocol for accessing a wide range of multifluoroalkenylated arenes. [ABSTRACT FROM AUTHOR]

Introduction: Ventricular assist devices (VADs) are considered an effective treatment for patients with advanced heart failure, while complications associated with blood damage remain a burden. Structure design innovation has the potential to reduce hemolysis and improve hemocompatibility. Methods: In this research, a novel mixed‐flow blood pump that integrates structural features of the axial and centrifugal VADs was proposed. The pump consists of an inducer, a mixed impeller supported by two ceramic pivot bearings, and a volute. The flow field and laminar viscous shear stress were analyzed by the in silico simulation. The hydraulic and hemolytic performance were evaluated in vitro by using a 3D printed pump. Results: The flow field distribution showed that streamlines in the connection area were smoothly transitioned through structural integration and no irregular flow occurred in the entire flow channel. The axial blades work as a fluid accelerator (generating 18.56% of the energy), and the centrifugal blades provide the main pressure head. The proportion of fluid inside the pump exposed to low laminar viscous shear stress (<50 Pa) and high laminar viscous shear stress (>150 Pa) was 99.02% and 0.03%, respectively. The in vitro hemolysis test results showed that the NIH (Normalized Index of Hemolysis) value of the mixed pump is 0.0079 ± 0.0039 g/100 L (n = 6). Conclusion: It can be concluded that the mixed flow structure is effective at improving hydraulic performance, eliminating flow disturbance, and minimizing shear stresses. This novel pump design is expected to provide a new direction for the development of next‐generation VADs. [ABSTRACT FROM AUTHOR]

• LDAOs are rich in quinone groups. • The redox of quinone groups realizes charge storage. • The feasibility of LDAOs as renewable charge storage materials was investigated. • Lignin structure significantly affects its energy storage performance. Lignin-derived aromatic oligomers (LDAOs) are the primary components of lignin depolymerization products. They are typically utilized as renewable crosslinking agents or resin materials with a considerably lower application value than aromatic monomers. Notably, LDAOs are rich in quinone groups, which enable storage and release of charges. In this work, the feasibility of LDAOs as renewable charge storage materials was investigated. LDAOs were first reacted with formaldehyde to generate a synthetic polymer (SP-AOF) via a phenol-formaldehyde condensation reaction. SP-AOF was subsequently incorporated with reduced graphene oxide (rGO), namely rGO/SP-AOF. As expected, the hybrid electrode exhibited high specific capacitance (250 F/g), which was approximately three times higher than that of rGO (87 F/g). This was due to the presence of quinone groups in SP-AOF, which could contribute to the overall capacitance with pseudocapacitance. Moreover, the hybrid electrode was able to deliver a high specific capacitance of 210 F/g even at a high specific current of 10 A/g. 1H−13C heteronuclear single quantum coherence nuclear magnetic resonance (2D HSQC NMR) and phosphorus nuclear magnetic resonance spectroscopy (31P NMR) analyses revealed that SP-AOF displayed higher quinone content (3.76 mmol/g) than commercially available lignin (organosolv and alkali lignin), which resulted in higher energy storage performance. This study provides a promising strategy for the utilization of aromatic oligomers as raw materials to manufacture high-performance lignin-derived energy storage materials. [ABSTRACT FROM AUTHOR]