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CHEMICAL ENGINEERING JOURNAL · 2019 · IF 8.355

Asymmetric alicyclic amine-polyether amine molecular chain structure for improved energy storage density of high-temperature crosslinked polymer capacitor

Siyu Chen,Guodong Meng,Bo Kong,Bing Xiao,Zhengdong Wang,Ziang Jing,Yushuan Gao,Guanglei Wu,Hong Wang,Yonghong Cheng

Crosslinked structure is proved to be efficient to improve breakdown strength ( E B ), thermal stability and charge-discharge efficiency ( η ) of polymer film capacitors, which is of great interest for their application in electric power systems and electrical automobile industry. However, highly crosslinked molecular networks usually lead to weak polarization ability of polymer, which greatly restrict their energy storage density ( U d ). To improve polymers’ high-field polarization ability while guaranteeing their E B and thermal stability, we propose the asymmetric molecular chain structure in crosslinked network of epoxy resin by attaching ring-like alicyclic amine (ACA) and linear polyether amine (PEA) on phenol via Mannich reaction. The film exhibits high U d up to 9.12 Jcm −3 at 550 MVm −1 and ambient temperature with 90% efficiency, which is a record high value for U d among single-layer polymer under the same condition. At 200 MVm −1 and 120 °C, a future operating condition towards electric-vehicle applications, prepared film still exhibits U d of 1 Jcm −3 with 90% efficiency, which is twice of the state-of-the-art BOPP. The results prove that the asymmetric ACA-PEA structure can greatly improve U d of crosslinked polymer film while maintaining superior energy storage efficiency at high temperature. This work paves a new way for the material design of high-performance polymer film capacitor.

研究领域: 材料科学 · 电气工程
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JOURNAL OF BIOLOGICAL CHEMISTRY · 2025 · IF 3.9

Multifunctional Molecular Agent for Tau-targeted Combinational Therapy of Alzheimer’s Disease

Junjie Wu,Keke Chai,Ying Tu,Kang Fang,Shuo Shi,Xiaochun Hu,Jihong Liu,Tianming Yao

Tau aggregation inhibitors or neurotoxic-metal chelators have been extensively studied as potential treatment for Alzheimer’s disease. However, it is a great challenge to improve their therapeutic effects while reducing neurotoxicity. Herein, we designed and synthesized two new compounds, (1,4,7,10-tetraazacyclododecane-1,4,7,10-tetrayl)tetrakis((3,4,5-trihydroxyphenyl)methanone) ( 4GA ) and (4,10-dimethyl-1,4,7,10-tetraazacyclododecane-1,7-diyl)bis((3,4,5-trihydroxyphenyl)methanone) ( 2GA ). Each molecule is composed of a 1,4,7,10-tetraazacyclododecane (cyclen) core as the supramolecular chelator to copper ions, attached by 2 or 4 gallic acid polyphenol arms to capture tau peptide chain like a molecular hairpin. We interestingly found 4GA and 2GA could inhibit self-aggregation through blocking the misfolding of tau peptide, suppress the promotion of Cu 2+ on tau aggregation by removing Cu 2+ from dyshomeostasis, and clear reactive oxygen species (ROS) triggered by Cu 2+ using their reductive gallic acid groups. More significantly, the synthesized compounds exhibit remarkable efficiency on both in vitro and at cellular level. Our rational design of multifunctional therapeutic agent that simultaneously targets tau misfolding process, copper dyshomeostasis and oxidative stress of ROS, may hold considerable implications for the treatment of AD.

研究领域: 神经科学 · 药物化学 · 生物无机化学 · 分子生物学 · 药理学
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