5 results match your criteria: "School of Chemistry and Molecular Engineering East China University of Science and Technology[Affiliation]"

Design of a Membrane-Anchored DNAzyme-Based Molecular Machine for Enhanced Cancer Therapy by Customized Cascade Regulation.

ACS Pharmacol Transl Sci

September 2024

Key Laboratory for Advanced Materials, Feringa Nobel Prize Scientist Joint Research Center, Joint International Laboratory for Precision Chemistry, Frontiers Science Center for Materiobiology & Dynamic Chemistry, School of Chemistry and Molecular Engineering East China University of Science and Technology, Shanghai 200237, P. R. China.

Synthetic DNAzyme-based structures enable dynamic cell regulation. However, engineering an effective and targeted DNAzyme-based structure to perform customizable multistep regulation remains largely unexplored. Herein, we designed a membrane-anchored DNAzyme-based molecular machine to implement dynamic inter- and intracellular cascade regulation, which realizes efficient T-cell/cancer cell interactions and subsequent receptor mediated cancer cell uptake.

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Size Reduction to Enhance Crystal-to-Liquid Phase Transition Induced by -to- Photoisomerization Based on Molecular Crystals of Phenylbutadiene Ester.

Materials (Basel)

July 2024

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering East China University of Science and Technology, 130 Meilong Road, Shanghai 200237, China.

Harnessing the photoinduced phase transitions in organic crystals, especially the changes in shape and structure across various dimensions, offers a fascinating avenue for exact spatiotemporal control, which is crucial for developing future smart devices. In our study, we report a new photoactive molecular crystal made from ()-2-(3-phenyl-allylidene)malonate (()-PADM). When exposed to ultraviolet (UV) light at 365 nm, this compound experiences an -to- photoisomerization in liquid solution and a crystal-to-liquid phase transition in solid crystals.

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Nickel-catalyzed acylation of vinylpyridine with alkylzincs under 1 atm CO.

Org Biomol Chem

March 2024

Key Laboratory for Advanced Materials and Joint International Research Laboratory of Precision Chemistry and Molecular Engineering, Feringa Nobel Prize Scientist Joint Research Center, Frontiers Science Center for Materiobiology and Dynamic Chemistry, School of Chemistry and Molecular Engineering East China University of Science and Technology, 130 Meilong Road, Shanghai, 200237, China.

A nickel-catalyzed acylation of vinylpyridines with CO at atmospheric pressure is reported, allowing for an expedient approach to synthesize β-acyl pyridine derivatives with high regio- and chemoselectivity. The electron-withdrawing property of pyridine plays pivotal roles in activating the alkenyl group, thereby facilitating this carbonylative process. In addition to vinylpyridines, other alkenylheterocycles such as thiazole and quinoline were also suitable for this method.

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For metal halide perovskite solar cells, bidentate passivation (BP) is highly effective, but currently, only passivation sites rather than molecular environments are being considered. Here, the authors report an effective approach for high-performance fully printable mesoscopic perovskite solar cells (FP-PSCs) through the BP strategy using the multidentate molecule 6-chloropurine (6-CP). By utilizing density functional theory (DFT) calculations, X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FTIR) characterizations, the competition mechanism is identified of BP between the chlorine atom and neighboring nitrogen atom of the imidazole and pyrimidine rings.

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Herein, we report the evaluation and synthesis of a reaction based fluorescent probe for the detection of Peroxynitrite (ONOO-). exhibits selective fluorescence off-on response for ONOO over other reactive oxygen species, including HO. Moreover, is biocompatible and has been used to visualize exogenous ONOO in HeLa cells.

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