产量(工程)
吸附
单层
甲醇
密度泛函理论
化学
材料科学
再现性
扩散
姜黄素
化学工程
氢
纳米技术
朗缪尔
金属有机骨架
朗缪尔吸附模型
计算化学
溶剂热合成
金属
有机化学
组合化学
作者
Büşra İpek,Zeynep Pinar Haslak,Bünyemin Çoşut,Hande Öztürk,İlknur Eruçar
出处
期刊:ACS omega
[American Chemical Society]
日期:2026-02-03
卷期号:11 (6): 10554-10567
被引量:4
标识
DOI:10.1021/acsomega.5c12081
摘要
Edible cyclodextrin-based metal organic frameworks (CD-MOFs) represent a sustainable platform for green synthesis. Yet, their reproducible synthesis remains a challenge for the MOF community. In this work, we explored the reproducibility of CD-MOF synthesis and resulting structural variations through five independent sample sets, each repeated three times via a controlled methanol vapor diffusion method. Increasing reaction temperature from 25 to 50 °C enhanced the thermodynamical favorability of γ-CD-MOF crystallization, as confirmed by Density Functional Theory (DFT) calculations. After identifying the optimized synthesis conditions that produced uniform cubic crystals with a high yield (83%), the resulting γ-CD-MOFs were tested for curcumin adsorption. The maximum loading capacity of curcumin reached 24.6%, with an equilibrium uptake of 1.5 mg/g at low concentrations, consistent with Langmuir monolayer adsorption. DFT calculations and molecular simulations revealed that hydrogen bonding, hydrophobic interactions, and strong host-guest affinity (∼65 kcal/mol) govern the adsorption process, predicting a maximum theoretical uptake capacity of 195.6 mg curcumin/g γ-CD-MOF. These results establish reproducible synthesis parameters and demonstrate the enhanced curcumin loading and stabilization capability of γ-CD-MOFs, underscoring their potential as efficient carriers for bioactive molecules.
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