Multicomponent coordination-driven self-assembly has proved to be a convenient approach to prepare advanced supramolecular coordination complexes (SCCs), especially for those with three-dimensional structures. Herein, we report the preparation of three tetragonal prismatic cages via the self-assembly of Pt(PEt)(OTf), three different linear dipyridyl ligands and porphyrin-based sodium benzoate ligands. Due to the efficient charge separation in the coordination process of Pt(PEt)(OTf) with pyridine and carboxylic acid and the directionality of metal-coordination bonds, these cages were prepared in high isolated yields (more than 90%). The absorption and emission properties as well as the singlet oxygen quantum yields of these cages were also studied, showing their potential applications as contrast agents for bio-imaging and photosensitizers for photodynamic therapy.
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http://dx.doi.org/10.1002/ijch.201800173 | DOI Listing |
Nanoscale
August 2024
New Chemistry Unit, School of Advanced Materials and International Centre for Material Science, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Jakkur P. O., Bengaluru-560064, India.
Layered transition metal dichalcogenides (TMDCs) are extensively investigated as catalyst materials for a wide range of electrochemical applications due to their high surface area and versatile electronic and chemical properties. Bulk TMDCs are van der Waals solids that possess strong in-plane bonding and weak inter-layer interactions. In the few-layer 2D TMDCs, several polymorphic structures have been reported as each individual layer can either retain octahedral or trigonal prismatic coordination.
View Article and Find Full Text PDFJ Am Chem Soc
March 2024
School of Chemistry and Chemical Engineering, Frontiers Science Center for Transformative Molecules and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, P. R. China.
Covalent organic cages are a prominent class of discrete porous architectures; however, their structural isomerism remains relatively unexplored. Here, we demonstrate the structural isomerism of chiral covalent organic cages that renders distinct enantioselective catalytic properties. Imine condensations of tetra-topic 5,10-di(3,5-diformylphenyl)-5,10-dihydrophenazine and ditopic 1,2-cyclohexanediamine produce two chiral [4 + 8] organic cage isomers with totally different topologies and geometries that depend on the orientations of four tetraaldehyde units with respect to each other.
View Article and Find Full Text PDFJ Am Chem Soc
February 2024
Yusuf Hamied Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom.
J Am Chem Soc
February 2024
Institut de Química Computacional i Catàlisi (IQCC) and Departament de Química, Universitat de Girona, Campus Montilivi, 17003 Girona, Catalonia, Spain.
Isomer-pure functionalized fullerenes are required to boost the development of fullerene chemistry in any field, but their multiple functionalization renders a mixture of regioisomers that are very difficult to purify by chromatography. For the specific case of C, its nonspherical geometry makes its regioselective functionalization more challenging than that of spherical C. In this work, the supramolecular mask approach is applied for the first time to C, which is encapsulated in two different nanocapsules to achieve the Bingel bis-cyclopropanation at α-bonds of opposite poles.
View Article and Find Full Text PDFJ Am Chem Soc
January 2024
School of Chemistry and Chemical Engineering, Anhui University of Technology, Ma'anshan 243032, P. R. China.
The construction of structurally well-defined supramolecular hosts to accommodate catalytically active species within a cavity is a promising way to address catalyst deactivation. The resulting supramolecular catalysts can significantly improve the utilization of catalytic sites, thereby achieving a highly efficient chemical conversion. In this study, the Co-metalated phthalocyanine () was successfully confined within a tetragonal prismatic metallacage, leading to the formation of a distinctive type of supramolecular photocatalyst ().
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