Three metal-organic frameworks with the general formula (BPZX = 3-X-4,4'-bipyrazolate, X = H, NH, NO) constructed with ligands having different functional groups on the same skeleton have been employed as heterogeneous catalysts for aerobic liquid-phase oxidation of cumene with O as oxidant. O adsorption isotherms collected at = 1 atm and = 195 and 273 K have cast light on the relative affinity of these catalysts for dioxygen. The highest gas uptake at 195 K is found for (3.2 mmol/g (10.1 wt % O)), in line with its highest BET specific surface area (926 m/g) in comparison with those of (317 m/g) and (645 m/g). The O isosteric heat of adsorption () trend follows the order > > . Interestingly, the selectivity in the cumene oxidation products was found to be dependent on the tag present in the catalyst linker: while cumene hydroperoxide (CHP) is the main product obtained with (84% selectivity to CHP after 7 h, = 4 bar, and = 363 K), further oxidation to 2-phenyl-2-propanol (PP) is observed in the presence of as the catalyst (69% selectivity to PP under the same experimental conditions).

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.inorgchem.0c00481DOI Listing

Publication Analysis

Top Keywords

metal-organic frameworks
8
heterogeneous catalysts
8
cobaltii bipyrazolate
4
bipyrazolate metal-organic
4
frameworks heterogeneous
4
cumene
4
catalysts cumene
4
cumene aerobic
4
oxidation
4
aerobic oxidation
4

Similar Publications

Glutathione-Responsive Metal-Organic-Framework-Derived MnO/(A/R)TiO Nanoparticles for Enhanced Synergistic Sonodynamic/Chemodynamic/Immunotherapy.

ACS Nano

January 2025

State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, 2699 Qianjin Street, Changchun 130012, China.

Despite the potential of sonodynamic therapy (SDT) in treating malignant tumors, the lack of effective sonosensitizers has limited its clinical implementation. In this study, we explored the relationship between the heteroatom doping concentration in metal-organic frameworks and interface formation after pyrolysis by regulating the addition of manganese sources and successfully derived Z-scheme heterojunctions MnO/(A/R)TiO (MTO) in situ from MIL-125-NH (Ti/Mn). The electron transfer pathway introduced by interfacial contact promoted carrier separation and greatly preserved the effective redox components, significantly influencing the performance of reactive oxygen species generation.

View Article and Find Full Text PDF

A smartphone-integrated colorimetric sensor is introduced for the rapid detection of phenolic compounds, including 8-hydroquinone (HQ), p-nitrophenol (NP), and catechol (CC). This sensor relies on the peroxidase-mimicking activity of aspartate-based metal-organic frameworks (MOFs) such as Cu-Asp, Ce-Asp, and Cu/Ce-Asp. These MOFs facilitate the oxidation of a colorless substrate, 3,3',5,5'-tetramethylbenzidine (TMB), by reactive oxygen species (ROS) derived from hydrogen peroxide (HO), resulting in the formation of blue-colored oxidized TMB (ox-TMB).

View Article and Find Full Text PDF

This perspective highlights the transformative potential of Metal-Organic Frameworks (MOFs) in environmental and healthcare sectors. It discusses work that has advanced beyond technology readiness levels of >4 including applications in capture, storage, and conversion of gases to value added products. This work showcases efforts in the most salient applications of MOFs which have been performed at a great cadence, enabled by the federal government, large companies, and startups to commercialize these technologies despite facing significant challenges.

View Article and Find Full Text PDF

An isoreticular metal-organic framework (MOF) series was constructed from nickel or cobalt nodes, phosphonate monoester, and bipyridine linkers. The cobalt-containing MOFs were found to catalyze the dehydrogenative C-H borylation of alkenes under mild conditions. This process selectively generates vinyl boronate without the formation of alkyl boronate byproducts and is insensitive to air, enabling large-scale preparation of the target products with isolated yields of over 80%.

View Article and Find Full Text PDF

This work presents the synthesis and characterization of three isomorphous lanthanide-based metal-organic frameworks (Ln-MOFs) (Ln3+ = Eu (1), Tb (2), and Sm (3)) supported by a pyridine-2,6-dicarboxamide-based linker offering appended arylcarboxylate groups. Single crystal X-ray diffraction studies highlight that these Ln-MOFs present three-dimensional porous architectures offering large cavities decorated with hydrogen bonding (H-bonding) groups. These Ln-MOFs display noteworthy luminescent characteristics.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!