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The construction of isotypic high-nuclearity inorganic cages with identical pristine parent structure and increasing nuclearity is highly important for molecular growth and structure-property relationship study, yet it still remains a great challenge. Here, we provide an in situ growth approach for successfully synthesizing a series of new giant hollow polymolybdate dodecahedral cages, , , and , whose structures are growth based on giant polymolybdate cage . Remarkably, they show two pathways of nuclear growth based on , that is, the growth of 10 and 20 Mo centers on the inner and outer surfaces to afford and , respectively, and the growth of 10 Mo centers both on the inner and outer surfaces to give . To the best of our knowledge, this is the first study to display the internal and external nuclear growth of a giant hollow polyoxometalate cage. More importantly, regular variations in structure and nuclearity confer these polymolybdate cages with different optical properties, oxidative activities, and hydrogen atom transfer effect, thus allowing them to exhibit moderate to excellent photocatalytic performance in oxidative cross-coupling reactions between different unactivated alkanes and N-heteroarenes. In particular, and with better comprehensive abilities can offer the desired coupling product with yield up to 92% within 1 h.
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http://dx.doi.org/10.1021/jacs.4c08043 | DOI Listing |
J Am Chem Soc
August 2024
Guangdong Provincial Key Laboratory of Carbon Dioxide Resource Utilization, School of Chemistry, South China Normal University, Guangzhou, Guangdong 510006, China.
The construction of isotypic high-nuclearity inorganic cages with identical pristine parent structure and increasing nuclearity is highly important for molecular growth and structure-property relationship study, yet it still remains a great challenge. Here, we provide an in situ growth approach for successfully synthesizing a series of new giant hollow polymolybdate dodecahedral cages, , , and , whose structures are growth based on giant polymolybdate cage . Remarkably, they show two pathways of nuclear growth based on , that is, the growth of 10 and 20 Mo centers on the inner and outer surfaces to afford and , respectively, and the growth of 10 Mo centers both on the inner and outer surfaces to give .
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2023
School of Chemistry, National and Local Joint Engineering Research Center of MPTES in High Energy and Safety LIBs, Engineering Research Center of MTEES (Ministry of Education), Key Lab. of ETESPG (GHEI), South China Normal University, 510006, Guangzhou, P. R. China.
Structural variants of high-nuclearity clusters are extremely important for their modular assembly study and functional expansion, yet the synthesis of such giant structural variants remains a great challenge. Herein, we prepared a lantern-type giant polymolybdate cluster (L-Mo ) containing equal metal nuclearity with the famous Keplerate type Mo (K-Mo ). The skeleton of L-Mo features a rare truncated rhombic triacontrahedron, which is totally different with the truncated icosahedral K-Mo .
View Article and Find Full Text PDFJ Am Chem Soc
August 2020
School of Chemistry, South China Normal University, Guangzhou 510006, P. R. China.
The synthesis of hollow opening polyhedral cages has always been an attractive but challenging goal, especially with regard to inorganic polyhedral cages. Herein, we present a novel, 240-nuclearity giant polymolybdate cage prepared via hydrothermal synthesis. This cage is composed of 20 tripod-shaped [MoO(SO)]/[MoO(SO)] building blocks with three connected vertices and 30 cubane-type [MoO] edge building blocks, featuring a rare, nearly regular pentagonal dodecahedron with a large inner cavity (diameter up to 1.
View Article and Find Full Text PDFJ Mater Chem B
January 2018
State Key Laboratory of Supramolecular Structure and Materials, College of Chemistry, Jilin University, Changchun, 130012, China.
A uniform ultra-small (<10 nm) nanosized dendritic composite was reported for combined photothermal-chemotherapy, wherein a giant ring-like polymolybdate cluster was introduced for the first time as a photothermal therapeutic agent. The giant polyoxometalate cluster possesses strong absorption characteristics in the near infrared region, whereas it has never been applied for biomaterials due to its sensitivity towards environment and structural instability under physiological conditions. Herein, a cationic dendron bearing triethylene glycol monomethyl ether terminal groups was used to cover a giant polyanionic cluster Mo surface through a simple electrostatic interaction.
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