The inaccessibility of uniform-diameter, single-chirality carbon nanotubes (CNTs) in pure form continues to thwart efforts by scientists to use these ultrathin materials in innovative applications that could revolutionize nanoscale electronics. Stimulated by the challenge to address this long-standing problem, we and other organic chemists have envisioned a new production strategy involving the controlled elongation of small hydrocarbon templates, such as hemispherical nanotube end-caps, prepared by bottom-up chemical synthesis; the diameter and rim structure encoded in the template would dictate the diameter and chirality of the resulting CNT. Toward that objective, a short [5,5] CNT has now been synthesized by stepwise chemical methods. This C(50)H(10) geodesic polyarene has been isolated, purified, crystallized, and fully characterized by NMR spectroscopy, UV-vis absorption spectroscopy, high resolution mass spectrometry, and X-ray crystallography.
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http://dx.doi.org/10.1021/ja209461g | DOI Listing |
Org Lett
January 2025
Key Laboratory of Precision and Intelligent Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China.
A 1,1-hydroboration of alkynylgermanes with unique -Ge/B stereochemistry under transition-metal-free conditions is reported. Mechanistic studies suggest that a pathway involving α-boration followed by a stepwise 1,2-Ge/H shift on the intermediate structurally lies between an alkyne-Ge π complex and a typical vinyl cation. The resulting Ge/B bimetallic modules, along with a /Ge/B trimetallic variant, can be conveniently transformed into trisubstituted olefins through iterative divergent cross-coupling.
View Article and Find Full Text PDFChem Commun (Camb)
January 2025
Jiangsu Key Laboratory of Function Control Technology for Advanced Materials, School of Environmental and Chemical Engineering Jiangsu Ocean University Lianyungang, Jiangsu 222005, China.
We propose an effective method for selectively extracting the valuable metals from the spent LiNiCoMnO cathode material using an oxalic acid-based deep eutectic solvent. Through regulation of the coordination environment, NiO, CoO, and MnO are stepwise separated and further applied in the electrochemical conversion of raw PET bottles to high-purity formic acid.
View Article and Find Full Text PDFChem Sci
January 2025
Department of Chemistry, University at Albany, State University of New York Albany New York 12222 USA
The chemical reduction of a pyracylene-hexa--hexabenzocoronene-(HBC)-fused nanographene TPP was investigated with K and Rb metals to reveal its multi-electron acceptor abilities. The reaction of TPP with the above alkali metals, monitored by UV-vis-NIR and H NMR spectroscopy, evidenced the stepwise reduction process. The use of different solvents and secondary ligands enabled isolation of single crystals of three different reduced states of TPP with 1, 2, and 3 electrons added to its π-system.
View Article and Find Full Text PDFAdv Healthc Mater
January 2025
National and Local Joint Engineering Research Center of Biomedical Functional Materials, School of Chemistry and Materials Science, Nanjing Normal University, Nanjing, 210023, China.
Bacterial infections can lead to severe medical complications, including major medical incidents and even death, posing a significant challenge in clinical trauma repair. Consequently, the development of new, efficient, and non-resistant antimicrobial agents has become a priority for medical practitioners. In this study, a stepwise hydrothermal reaction strategy is utilized to prepare FeO@MoS core-shell nanoparticles (NPs) with photosynthesis-like activity for the treatment of bacterial infections.
View Article and Find Full Text PDFNat Commun
January 2025
Beijing National Laboratory for Molecular Sciences (BNLMS), State Key Laboratory of Rare Earth Materials Chemistry and Applications, PKU-HKU Joint Laboratory in Rare Earth Materials and Bioinorganic Chemistry, College of Chemistry and Molecular Engineering, Peking University, Beijing, China.
Dual active sites with synergistic valence state regulation under oxidizing and reducing conditions are essential for catalytic reactions with step-wise mechanisms to modulate the complex adsorption sites of reactant molecules on the surfaces of heterogeneous catalysts with maximized catalytic performances, but it has been rarely explored. In this work, uniformly dispersed CuCo alloy and CoO nanosheet composite catalysts with dual active sites are constructed, which shows huge boost in activity for catalyzing water-gas shift reaction (WGSR), with a record high reaction rate reaching 204.2 μmol g s at 300 °C for CuCoO amongst the reported Cu-based and Co-based catalysts.
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