A new metal-organic polyhedron with a high surface area of 407 m g, possessing high CO uptake, is reported, which is synthesized using 4-connected Cu(CO) paddle-wheel moieties and 3-connected semi-rigid tripodal carboxylates. This material possesses a high density of Cu(II) Lewis acidic sites and demonstrates excellent performance as a heterogeneous catalyst for the chemical fixation of CO into cyclic carbonates under ambient conditions.

Download full-text PDF

Source
http://dx.doi.org/10.1039/d2cc01734bDOI Listing

Publication Analysis

Top Keywords

metal-organic polyhedron
8
polyhedron high
8
high uptake
8
ambient conditions
8
[ml] metal-organic
4
high
4
uptake efficient
4
efficient chemical
4
chemical conversion
4
conversion ambient
4

Similar Publications

Confining CoSe/MoSe2 Heterostructures in Interconnected Carbon Polyhedrons for Superior Potassium Storage.

ChemSusChem

January 2025

Jilin University, School of Materials Science and Engineering, Renmin street 5988, School of Materials Science and Engineering, Jilin University, 130022, Changchun, CHINA.

Metal selenides hold promise as feasible anode materials for potassium-ion batteries (PIBs), but still face problems such as poor potassium storage kinetics and dramatic volume expansion. Coupling heterostructure engineering with structural design could be an effective strategy for rapid and stable K+ storage. Herein, CoSe/MoSe2 heterojunction encapsulated in nitrogen-doped carbon polyhedron and further interconnected by three-dimensional nitrogen-doped carbon nanofibers (CoMoSe@NCP/NCFs) is ingeniously constructed.

View Article and Find Full Text PDF

The reaction between molybdenum(ii) acetate and 5-aminoisophthalic acid (HIso-NH) afforded [MoO(μ-O)(Iso-NH)], a novel molybdenum(v) metal-organic polyhedron (MOP) with a triangular antiprismatic shape stabilized by intramolecular N-H⋯O hydrogen bonds. The synthesis conditions, particularly the choice of solvent and reaction time, led to the precipitation of the Mo(v)-MOP in five distinct crystalline forms. These forms vary in their packing arrangements, co-crystallized solvent molecules, and counter-cations, with three phases containing dimethylammonium (dma) and the other two containing diethylammonium (dea).

View Article and Find Full Text PDF

Space Exploration of Metal-Organic Frameworks in the Mesopore Regime.

Acc Chem Res

January 2025

Key Laboratory of Biomedical Polymers, Ministry of Education, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.

ConspectusThe past decades have witnessed the proliferation of porous materials offering high surface areas and the revolution in gas storage and separation, where metal-organic frameworks (MOFs) stand out as an important family. Alongside the pursuit of higher surface area, the increase in the size of guests, such as nanoparticles and biomolecules, has also led to the demand for larger space defined by the pores and cages within the MOF structure, from the conventional micropore regime (<2 nm) toward the mesopore regime (2-50 nm). Among the essential elements in the design of MOFs, molecular building blocks, their coordination and spatial arrangement, the chemistry for molecular design, and coordination bonds have become relatively mature, offering precise control of the shape and environment of the molecularly defined 3D cages; however, the correlation between the geometrical parameters and the size of polyhedrons describing the cages, concerning the spatial arrangement of building blocks, is much less explored.

View Article and Find Full Text PDF

The controllable encapsulation of host molecules (such as porphyrin, phthalocyanine, crown ether, calixarene or cucurbituril organic macrocycles, cages, metal-organic polyhedrons and enzymes) into the pores of metal-organic frameworks (MOFs) to form host-in-host (host@MOF) materials has attracted increasing research interest in various fields. These host@MOF materials combine the merits of MOFs as a host matrix and functional host molecules to exhibit synergistic functionalities for the formation of guest@host@MOF materials in sorption and separation, ion capture, catalysis, proton/ion conduction and biosensors. (This guest@host@MOF construction is reminiscent of Russian (Matrjoschka) dolls which are nested dolls of decreasing size placed one inside another.

View Article and Find Full Text PDF

Tc is one of the potentially toxic radioactive substances owing to its long half-life and a high degree of environmental mobility. Hence, the sequestration of Tc from radioactive waste has become enormously important and a contemporary research priority. However, selective extraction of this species in its stable oxoanionic form (TcO ) is very challenging on account of bottlenecks such as low charge density, less hydrophilic nature, Herein, an ultrathin hybrid composite material has been strategically designed and fabricated by covalent anchoring of a chemically stable amino functionalized nanosized cationic metal-organic polyhedron with a positively charged robust ionic covalent organic framework.

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!