Amsharov

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Organization: Max Planck Institute for Solid State Research
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Co-reporter:Dr. A. Kromer;Dr. U. Wedig; E. Roduner; M. Jansen;Dr. Konstantin Yu. Amsharov
Angewandte Chemie International Edition 2013 Volume 52( Issue 48) pp:12610-12614
Publication Date(Web):
DOI:10.1002/anie.201305808
Co-reporter:Dr. A. Kromer;Dr. U. Wedig; E. Roduner; M. Jansen;Dr. Konstantin Yu. Amsharov
Angewandte Chemie 2013 Volume 125( Issue 48) pp:12842-12846
Publication Date(Web):
DOI:10.1002/ange.201305808
Co-reporter:Dr. Mikhail Kabdulov;Dr. Martin Jansen ;Dr. Konstantin Yu. Amsharov
Chemistry - A European Journal 2013 Volume 19( Issue 51) pp:17262-17266
Publication Date(Web):
DOI:10.1002/chem.201303838
Co-reporter:Andreas Mueller ;Konstantin Yu. Amsharov
European Journal of Organic Chemistry 2012 Volume 2012( Issue 31) pp:6155-6164
Publication Date(Web):
DOI:10.1002/ejoc.201200841

Abstract

We report herein the synthesis of six precursor molecules for the rational synthesis of isomerically pure armchair, zigzag, or chiral single-walled carbon nanotubes (SWCNTs). The polycyclic aromatic hydrocarbons possess the required carbon connectivity for the generation of extended hemispherical buckybowls with predefined geometry through intramolecular cyclodehydrogenation. The precursors for the short carbon nanotubes and the large-diameter hemispherical buckybowls have potential for the rational initiation of single-chirality SWCNT growth on metal surfaces. The options for the construction of precursors for various SWCNT chiralities based on the suggested synthesis strategy are presented.

Co-reporter:Andreas Mueller ;Konstantin Yu. Amsharov
European Journal of Organic Chemistry 2012 Volume 2012( Issue 36) pp:
Publication Date(Web):
DOI:10.1002/ejoc.201201448

No abstract is available for this article.

Co-reporter:K. Yu. Amsharov;M. A. Kabdulov ;Dr. Martin Jansen
Angewandte Chemie International Edition 2012 Volume 51( Issue 19) pp:4594-4597
Publication Date(Web):
DOI:10.1002/anie.201200516
Co-reporter:K. Yu. Amsharov;M. A. Kabdulov ;Dr. Martin Jansen
Angewandte Chemie 2012 Volume 124( Issue 19) pp:4672-4675
Publication Date(Web):
DOI:10.1002/ange.201200516
Co-reporter:K.Yu. Amsharov and P. Merz
The Journal of Organic Chemistry 2012 Volume 77(Issue 12) pp:5445-5448
Publication Date(Web):May 24, 2012
DOI:10.1021/jo300783y
A strategy for effective intramolecular aryl–aryl coupling of fluoroarenes through Al2O3-mediated HF elimination is reported. It is demonstrated that the C–F bond, which is widely believed to be the most passive functionality in organic chemistry, can be reconsidered as a useful functional group allowing very effective C–C bond formation. The solid-state strategy presented in this study opens the possibility for facile syntheses of insoluble extended polycyclic aromatic hydrocarbons.
Co-reporter:Mikhail A. Kabdulov, Konstantin Yu. Amsharov, Martin Jansen
Tetrahedron 2010 66(45) pp: 8587-8593
Publication Date(Web):
DOI:10.1016/j.tet.2010.09.055
Co-reporter:KonstantinYu. Amsharov Dr.;MikhailA. Kabdulov ;Martin Jansen
Chemistry - A European Journal 2010 Volume 16( Issue 20) pp:5868-5871
Publication Date(Web):
DOI:10.1002/chem.201000374
Co-reporter:Konstantin Yu. Amsharov;Mikhail A. Kabdulov ;Martin Jansen
European Journal of Organic Chemistry 2009 Volume 2009( Issue 36) pp:6328-6335
Publication Date(Web):
DOI:10.1002/ejoc.200900976

Abstract

Various functional groups have been tested as alternative promoters of the intramolecular condensation of benzo[c]phenanthrene under flash vacuum pyrolysis conditions. Methyl and fluorine functionalization were found to be promising approaches. Unexpectedly high selectivity was observed in the cyclization of fluorinated benzo[c]phenanthrenes. The mechanism for the condensation reaction and the advantages of fluorine as a promoter for the rational synthesis of fullerenes are discussed.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)

1,1':2',1''-TERPHENYL, 4-METHYL-
Triphenylene, 2-methyl-