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Research on the synthesis of catenated cages has been a growing field of interest in the past few years. While multiple types of catenated cages with different structures have been synthesized, the application of such systems has been much less explored. Specifically, the use of catenated cages in the separation of industrially relevant molecules that are present in coal tar has not been explored before. Herein, we demonstrate the use of a newly synthesized interlocked cage [CHNOPd] (), formed through the self-assembly of ligand (tris(4-(1-imidazole-1-yl)benzylidene)hydrazine-1-carbohydrazonhydrazide) with acceptor -[(tmchda)Pd(NO)] [tmchda = ±,,','-tetramethylcyclohexane-1,2-diamine] (). The interlocked cage was able to separate the isomers (anthracene and phenanthrene) using a simple solvent extraction technique. Using the same technique, the much more difficult separation of structurally and physiochemically similar compounds acenaphthene and acenaphthylene was performed for the first time with as the host. Other noninterlocked hexanuclear Pd cages having a wider cavity proved inefficient for such separation, demonstrating the uniqueness of the interlocked cage for such challenging separation.
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http://dx.doi.org/10.1021/acs.inorgchem.4c01376 | DOI Listing |
Nat Rev Chem
August 2025
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, Shanghai, China.
Mechanically interlocked molecules, including catenanes, rotaxanes and knots, are an intriguing class of synthetic targets with potential applications in molecular switches and machines. Although mechanically interlocked molecules are typically constructed using macrocyclic frameworks, the interlocking of two or more three-dimensional, shape-persistent cages remains relatively underexplored. Recent advances have accelerated the development of mechanically interlocked cages (MICs), which consist of interlocked three-dimensional molecular cages rather than macrocycles.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2025
Department of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn Straße 6, 44227, Dortmund, Germany.
Precise control over the catenation process in interlocked supramolecular systems remains a significant challenge. Here, we report a system in which a lantern-shaped PdL cage can dimerize to form two distinct PdL catenanes with different interlocking degree: a previously described quadruply interlocked double cage motif of D symmetry and an unprecedented triply interlocked structure of C symmetry. While the former structure features a linear arrangement of four Pd(II) centers, separated by three mechanically linked pockets, the new motif has a staggered shape.
View Article and Find Full Text PDFInorg Chem
August 2024
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bangalore 560012, India.
Research on the synthesis of catenated cages has been a growing field of interest in the past few years. While multiple types of catenated cages with different structures have been synthesized, the application of such systems has been much less explored. Specifically, the use of catenated cages in the separation of industrially relevant molecules that are present in coal tar has not been explored before.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2024
State Key Laboratory for Mechanical Behavior of Materials, Shaanxi International Research Center for Soft Matter, School of Materials Science and Engineering, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.
Although catenated cages have been widely constructed due to their unique and elegant topological structures, cyclic catenanes formed by the connection of multiple catenane units have been rarely reported. Herein, based on the orthogonal metal-coordination-driven self-assembly, we prepare a series of heterometallic [2]catenanes and cyclic bis[2]catenanes, whose structures are clearly evidenced by single-crystal X-ray analysis. Owing to the multiple positively charged nature, as well as the potential synergistic effect of the Cu(I) and Pt(II) metal ions, the cyclic bis[2]catenanes display broad-spectrum antibacterial activity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
March 2023
Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany.
Mechanically interlocked structures are fascinating synthetic targets and the topological complexity achieved through catenation offers numerous possibilities for the construction of new molecules with exciting properties. In the structural space of catenated organic cage molecules, only few examples have been realized so far, and control over the catenation process in solution is still barely achieved. Herein, we describe the formation of a quadruply interlocked catenane of giant chiral [8+12] salicylimine cubes.
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