Since the first proposal that fullerenes are capable of hosting atoms, ions, or clusters by the late Smalley in 1985, tremendous examples of endohedral metallofullerenes (EMFs) have been reported. Breaking the dogma that monometallofullerenes (mono-EMFs) always exist in the form of M@C2n while clusterfullerenes always require multiple (two to four) metal cations to stabilize a cluster that is unstable as a single moiety, here we show an unprecedented monometallic endohedral clusterfullerene entrapping an yttrium cyanide cluster inside a popular C82 cage--YCN@C(s)(6)-C82. X-ray crystallography and (13)C NMR characterization unambiguously determine the cage symmetry and the endohedal cyanide structure, unexpectedly revealing that the entrapped YCN cluster is triangular. The unprecedented monometallic clusterfullerene structure unveiled by YCN@C(s)(6)-C82 opens up a new avenue for stabilizing a cluster by a single metal cation within a carbon cage, and will surely stimulate further studies on the stability and formation mechanism of EMFs.
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http://dx.doi.org/10.1038/srep01487 | DOI Listing |
Phys Chem Chem Phys
October 2024
Instituto de Investigaciones en Catálisis y Petroquímica "Ingeniero José M. Parera" (INCAPE), Facultad de Ingeniería Química, Universidad Nacional del Litoral - CONICET, Centro Científico Tecnológico CONICET Santa Fe (CCT-SF), Santa Fe, Argentina.
In this work, supported Pt monometallic catalysts were prepared using oxide and carbon supports by conventional impregnation methods. Similar Pt metallic nanoparticle sizes (mean sizes about 1.8-2 nm) have been obtained using different Pt precursor loadings (0.
View Article and Find Full Text PDFACS Appl Bio Mater
September 2024
Department of Pharmacology, Saveetha Dental College, and Hospitals, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai 600077, Tamil Nadu, India.
Nanofluids hold significant promise in diverse applications, particularly in biomedicine, where noble trimetallic nanofluids outperformed their monometallic counterparts. The composition, morphology, and size of these nanofluids play pivotal roles in their functionality. Controlled synthesis methods have garnered attention, focusing on precise morphology, content, biocompatibility, and versatile chemistry.
View Article and Find Full Text PDFInorg Chem
September 2023
Department of Chemistry, University of Bath, Bath BA2 7AY, U.K.
We report three niobium-based initiators for the catalytic ring-opening polymerization (ROP) of ε-caprolactone, exhibiting good activity and molecular weight control. In particular, we have prepared on the gram-scale and fully characterized a monometallic cationic alkoxo-Nb(V) ε-caprolactone adduct representing, to the best of our knowledge, an unprecedented example of a metal complex with an intact lactone monomer and a functional ROP-initiating group simultaneously coordinated at the metal center. At 80 °C, all three systems initiate the immortal solution-state ROP of ε-caprolactone via a coordination-insertion mechanism, which has been confirmed through experimental studies, and is supported by computational data.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
February 2022
Univ Rennes, CNRS, ISCR, Institut des Sciences Chimiques de Rennes)-UMR 6226, 35000, Rennes, France.
By their conformational flexibility, Möbius aromatic hexaphyrins provide a dynamic chirality attractive to develop stimuli responsive systems such as chiroptical switches. A regular [28]hexaphyrin has been equipped with a chiral coordinating arm to achieve transfer of chirality from a fix stereogenic element to the dynamic Möbius one. The arm allows straightforward formation of labile monometallic Zn complexes with an exogenous ligand, either a carboxylato or an amino with opposite inwards/outwards orientations relative to the Möbius ring.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2019
Department of Chemistry and Biochemistry, University of South Carolina, Columbia, SC, 29208, USA.
We report the first study of a gas-phase reaction catalyzed by highly dispersed sites at the metal nodes of a crystalline metal-organic framework (MOF). Specifically, CuRhBTC (BTC =benzenetricarboxylate) exhibited hydrogenation activity, while other isostructural monometallic and bimetallic MOFs did not. Our multi-technique characterization identifies the oxidation state of Rh in CuRhBTC as +2, which is a Rh oxidation state that has not previously been observed for crystalline MOF metal nodes.
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