Academic Journal
A General Base-free Route toward the Building of Metal N‑Heterocyclic Carbenes into Covalent Organic Frameworks for CO 2 Conversion
العنوان: | A General Base-free Route toward the Building of Metal N‑Heterocyclic Carbenes into Covalent Organic Frameworks for CO 2 Conversion |
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المؤلفون: | Chang He, Duan-Hui Si, Lili Han, Zhong-Ning Xu, Ziao Chen, Rong Cao, Yuan-Biao Huang |
سنة النشر: | 2024 |
مصطلحات موضوعية: | Biophysics, Biochemistry, Molecular Biology, Developmental Biology, Cancer, Space Science, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, performing heterogeneous catalysts, offering combined advantages, noteworthy turnover frequency, immobilize metal n, functionalized porous materials, covalent organic frameworks, corresponding metal complexes, nhc single sites, highly efficient catalysts, facile synthesis method, free route toward, nhc – cof, 2 sub, nhc – cofs, nhc – co, general strategy would, free strategy, general base, facile base, efficient co |
الوصف: | Covalent organic frameworks (COFs) would be a promising platform to immobilize metal N-heterocyclic carbenes (M-NHCs) for efficient CO 2 conversion, but they are seldom reported. Herein, we develop a facile base-free strategy to prepare M-NHCs (M = Ir, Au, Pd) decorated M-NHC–COFs (Ir-NHC–COF, Au-NHC–COF, and Pd-NHC–COF) via the reactions of the imidazolium carboxylate functionalized NHC-based COF (NHC–CO 2 –COF) with the corresponding metal complexes under mild conditions. This facile synthesis method for the generation of the desired M-NHC single sites avoids the handling of the free carbenes and the use of strong bases. The obtained Ir-NHC–COF catalyst showed efficient catalytic activity and recyclability in the CO 2 hydrogenation process, attaining a noteworthy turnover frequency of up to 17244 h –1 , which placed it among the top-performing heterogeneous catalysts for this reaction. This study presents a universal and straightforward approach for attaching functional M-NHC single sites onto COFs, offering combined advantages and acting as highly efficient catalysts for CO 2 hydrogenation reactions. This general strategy would be widely applicable to prepare other M-NHC-functionalized porous materials with covalently bound M-NHC single sites for various applications in the future. |
نوع الوثيقة: | article in journal/newspaper |
اللغة: | unknown |
Relation: | https://figshare.com/articles/journal_contribution/A_General_Base-free_Route_toward_the_Building_of_Metal_N_Heterocyclic_Carbenes_into_Covalent_Organic_Frameworks_for_CO_sub_2_sub_Conversion/25302015 |
DOI: | 10.1021/acscatal.4c00037.s001 |
الاتاحة: | https://doi.org/10.1021/acscatal.4c00037.s001 https://figshare.com/articles/journal_contribution/A_General_Base-free_Route_toward_the_Building_of_Metal_N_Heterocyclic_Carbenes_into_Covalent_Organic_Frameworks_for_CO_sub_2_sub_Conversion/25302015 |
Rights: | CC BY-NC 4.0 |
رقم الانضمام: | edsbas.9F11F1AB |
قاعدة البيانات: | BASE |
DOI: | 10.1021/acscatal.4c00037.s001 |
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