4.8 Article

MOF Polymer Composites Exhibit Faster Nitric Oxide Catalysis than MOF Crystallites

期刊

ACS MATERIALS LETTERS
卷 4, 期 12, 页码 2434-2439

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AMER CHEMICAL SOC
DOI: 10.1021/acsmaterialslett.2c00742

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  1. National Institutes of Health [5R01HL140301]
  2. Assistant Secretary of Defense for Health Affairs [W81XWH-18-2-0048]

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This study compares the release of nitric oxide (NO) from unprocessed metal-organic frameworks (MOF) powders and MOF-polymer composites as catalysts. The results show that the rate of NO generation changes when a polymer composite is used as the catalyst, indicating that the findings for MOF powder catalysts may not always be applicable to MOF-polymer composites.
Metal-organic frameworks (MOFs), a class of crystalline solids, show promise for application as heterogeneous catalysts. Applying MOFs in industrial settings usually requires that unprocessed MOF powder be immobilized within a continuous phase, such as a polymer; however, it is unknown in general if this immobilization impacts MOF catalyst behavior. Therefore, it is necessary to directly compare unprocessed MOF powders and MOF-polymer composites as catalysts. Herein, we study the biomedically important release of nitric oxide (NO) from endogenous S-nitrosoglutathione (GSNO) catalyzed by the unprocessed powder and polymer composite forms of H3[(Cu4Cl)3(BTTri)8] (CuBTTri). The NO release system is especially appropriate as CuBTTri has found real-world application in the field of biomedical materials. The results show, in this system, that the rate of NO generation changes when a CuBTTri polymer composite is the catalyst as opposed to the unprocessed MOF powder. Hence, findings for MOF powder catalysts may not always translate to MOF-polymer composites.

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