纳米反应器
催化作用
化学
星团(航天器)
铜
基质(水族馆)
组合化学
化学工程
有机化学
计算机科学
海洋学
地质学
工程类
程序设计语言
作者
Wan‐Zhen Qiao,Baojing Xue,Rui Wang,Yuan Yang,Shuang‐Quan Zang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-06-30
卷期号:64 (35): e202511580-e202511580
被引量:4
标识
DOI:10.1002/anie.202511580
摘要
Chemical fixation of CO2 with propargylic amines/alcohols into high value-added fine chemicals represents promising and practical routes for CO2 resource utilization, but it remains a great challenge to achieve low-concentration CO2 conversion in both reactions through one single catalytic system. Herein, a robust copper cluster [(C6H15NH)(Cu8L8I)] (I@Cu8) with nanosized cavities has been constructed. Importantly, the I@Cu8 cluster as a nanoreactor can efficiently catalyze the chemical conversion of both propargylic amines and propargylic alcohols with CO2 at simulated flue gas concentrations, due to the unique substrate enrichment effect of its well-defined nanocavities. Catalytic mechanism investigation and DFT calculations illustrate that the excellent catalytic performance originates from the simultaneous activation of alkynyl (─C≡CH) bonds and amino/hydroxyl (─NHR/─OH) groups in the I@Cu8 catalytic system, in which the I@Cu8-substrate intermediates have been confirmed through ESI-MS analysis. Impressively, this is the first example of a cluster-based nanoreactor catalyst for low-concentration CO2 cyclization reactions with both propargylic amines and propargylic alcohols. This work provides a foundation for the construction of metal cluster-based catalysts for CO2 conversion into valuable chemicals.
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