Synthesis of cyclo[18]carbon via debromination of C18Br6

التفاصيل البيبلوغرافية
العنوان: Synthesis of cyclo[18]carbon via debromination of C18Br6
المؤلفون: Steffen L. Woltering, Harry L. Anderson, Lorel M. Scriven, Leo Gross, Przemyslaw Gawel, Katharina Kaiser, Kirsten E. Christensen, Alistair J. Sterling, Fabian Schulz
المصدر: Journal of the American Chemical Society, vol 142, iss 30
Journal of the American Chemical Society
بيانات النشر: American Chemical Society, 2020.
سنة النشر: 2020
مصطلحات موضوعية: Polyyne, Communication, Bilayer, Sodium, Oxide, Alternation (geometry), Halogenation, Cumulene, chemistry.chemical_element, General Chemistry, 010402 general chemistry, 01 natural sciences, Biochemistry, Catalysis, 0104 chemical sciences, chemistry.chemical_compound, Crystallography, Colloid and Surface Chemistry, chemistry, Chemical Sciences, Cyclocarbon
الوصف: Cyclo[18]carbon (C18, a molecular carbon allotrope) can be synthesized by dehalogenation of a bromocyclocarbon precursor, C18Br6, in 64% yield, by atomic manipulation on a sodium chloride bilayer on Cu(111) at 5 K, and imaged by high-resolution atomic force microscopy. This method of generating C18gives a higher yield than that reported previously from the cyclocarbon oxide C24O6. The experimental images of C18were compared with simulated images for four theoretical model geometries, including possible bond-angle alternation:D18hcumulene,D9hpolyyne,D9hcumulene, andC9hpolyyne. Cumulenic structures, with (D9h) and without (D18h) bond-angle alternation, can be excluded. Polyynic structures, with (C9h) and without (D9h) bond-angle alternation, both show a good agreement with the experiment and are challenging to differentiate.
وصف الملف: application/pdf
اللغة: English
DOI: 10.1021/jacs.0c05033
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53b6534ee5f07c67b77188ad696173c0
https://doi.org/10.1021/jacs.0c05033
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....53b6534ee5f07c67b77188ad696173c0
قاعدة البيانات: OpenAIRE