催化作用
材料科学
水溶液
水解
限制
粒子(生态学)
生物相容性材料
纳米技术
组合化学
水介质
工作(物理)
矿化(土壤科学)
动力学
原位
化学工程
化学
粒径
密度泛函理论
航程(航空)
催化效率
纳米尺度
酶催化
定义明确
酶
静电学
作者
Jesús Cases Díaz,Joaquín Calbo,Mónica Giménez‐Marqués
标识
DOI:10.1021/acsami.6c09388
摘要
Hydrolytically unstable metal-organic frameworks (MOFs) remain difficult to synthesize under aqueous, biocompatible conditions, limiting their integration with biomacromolecules. Here, we report a polyol-assisted aqueous strategy for the synthesis of highly crystalline HKUST-1 with tunable particle size under mild conditions. Polyols act as cosolvents that promote framework formation while enabling precise control over particle size through modulation of precursor concentration. Combined experimental studies and density functional theory calculations reveal that polyols stabilize the Cu(II) paddlewheel secondary building units against water-mediated hydrolysis, thereby enabling crystalline HKUST-1 formation in water. Importantly, these synthetic conditions are fully compatible with in situ protein encapsulation. Proteins spanning a broad range of electrostatic properties were successfully incorporated, yielding protein@HKUST-1 biocomposites that preserve structural integrity and retain enzymatic activity over multiple catalytic cycles. This work establishes a practical strategy for stabilizing hydrolytically unstable MOFs during aqueous synthesis, and broadens their integration with biomacromolecules for biotechnological and biomedical applications.
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