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Zirconium-metalloporphyrin PCN-222: mesoporous metal-organic frameworks with ultrahigh stability as biomimetic catalysts.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Feng, Dawei Gu, Zhi-yuan Li, Jian-rong Jiang, Hai-Long Wei, Zhangwen Zhou, Hai Yun |
| Copyright Year | 2012 |
| Abstract | In nature, metalloporphyrins are well known for performing many biological functions in aqueous media, such as light harvesting, oxygen transportation, and catalysis. Heme, the iron–porphyrin derivative, is the cofactor for many enzyme/ protein families, including peroxidases, cytochromes, hemoglobins, and myoglobins. Using synthetic systems to mimic natural enzymes with high catalytic activity and substrate selectivity has been a sought-after goal in the last decade. Direct application of a heme as an oxidation catalyst in aqueous solution is usually challenging due to the formation of catalytically inactive dimers and catalyst self-destruction in the oxidizing reaction media. One promising approach is to load heme on supports, such as zeolites, clays, nanoparticles, hydrogels, or carbon materials, a practice which inevitably dilutes the density of active sites. An alternative approach is to protect the heme center by modifying the porphyrin to produce dendrimers or molecular crystals, which is a synthetically demanding method. Herein, we propose a unique strategy employing heme-like active centers as structural motifs for the assembly of highly stable porous materials, which should possess well-defined mesochannels and ultrahigh stability in aqueous solution. Metal-organic frameworks (MOFs) are a new class of crystalline porous materials with fascinating structures and intriguing properties, such as permanent porosity, high surface area, and uniform open cavities. The availability of various building blocks consisting of metals and organic linkers makes it possible to construct MOFs with unique properties for diverse applications. However, these desirable features of MOFs have rarely been applied to an enzymatic mimic, especially for catalysis in an aqueous medium, despite the fact that the assembly of ligands bearing high-density active sites into 3D frameworks may provide an ideal system to both enhance the catalytic activity and protect the cofactors. One of the main reasons is the lack of water-stable MOFs containing redox-active metal centers. Furthermore, most MOFs are microporous (pore size< 2 nm). Although they are suitable for gas storage, the small pore size slows down diffusion and limits the access of large substrate molecules to the active sites inside a MOF. Therefore, MOFs with mesopores, accessible redox sites, and ultrahigh stability, especially in aqueous media, are indispensible for any successful biomimetic attempt. Herein we have employed Fe-TCPP (TCPP= tetrakis(4carboxyphenyl)porphyrin) as a heme-like ligand and chosen highly stable Zr6 clusters as nodes for the assembly of stable Zr-MOFs. With carefully selected starting materials, we have successfully constructed a 3D heme-like MOF, designated as PCN-222(Fe) (Figure 1; PCN= porous coordination net- |
| Starting Page | 133 |
| Ending Page | 133 |
| Page Count | 1 |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://chem.rutgers.edu/sites/default/files/02-05-2013%20-%20Zhou,%20Joe%20-%20Abstract%20-%20Zirconium.pdf |
| Alternate Webpage(s) | http://staff.ustc.edu.cn/~jianglab/fulltexts/36.pdf |
| PubMed reference number | 22907870v1 |
| Alternate Webpage(s) | https://doi.org/10.1002/anie.201204475 |
| DOI | 10.1002/anie.201204475 |
| Journal | Angewandte Chemie |
| Volume Number | 51 |
| Issue Number | 41 |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | Biomimetics Catalysis Dendrimers Ephrin Type-B Receptor 1, human Heme Hemoglobin Hydrogels Inactive - Biochemical Activity Level Iron Ligands Material Pore Size Metalloporphyrins Metals Myoglobin Oxygen Peroxidases Porphyrins Solute Carrier Organic Anion Transporter Family Member 1b1 Zeolites Zirconium chemical cofactor clay enzyme activity oxidation tetracarboxyphenylporphine |
| Content Type | Text |
| Resource Type | Article |
