Andrey A. Fokin
Andrey A. Fokin
National Technical University of Ukraine Kiev Polytechnic Institute
Verified email at - Homepage
Cited by
Cited by
Selective alkane transformations via radicals and radical cations: Insights into the activation step from experiment and theory
AA Fokin, PR Schreiner
Chemical reviews 102 (5), 1551-1594, 2002
Diamonds are a chemist's best friend: diamondoid chemistry beyond adamantane
H Schwertfeger, AA Fokin, PR Schreiner
Angewandte Chemie International Edition 47 (6), 1022-1036, 2008
Many density functional theory approaches fail to give reliable large hydrocarbon isomer energy differences
PR Schreiner, AA Fokin, RA Pascal, A de Meijere
Organic Letters 8 (17), 3635-3638, 2006
Overcoming lability of extremely long alkane carbon–carbon bonds through dispersion forces
PR Schreiner, LV Chernish, PA Gunchenko, EY Tikhonchuk, ...
Nature 477 (7364), 308-311, 2011
How accurate are DFT treatments of organic energies?
MD Wodrich, C Corminboeuf, PR Schreiner, AA Fokin, PR Schleyer
Organic letters 9 (10), 1851-1854, 2007
One-dimensional aggregation of regioregular polyalkylthiophenes
N Kiriy, E Jähne, HJ Adler, M Schneider, A Kiriy, G Gorodyska, S Minko, ...
Nano Letters 3 (6), 707-712, 2003
Monochromatic electron photoemission from diamondoid monolayers
WL Yang, JD Fabbri, TM Willey, JRI Lee, JE Dahl, RMK Carlson, ...
Science 316 (5830), 1460-1462, 2007
Stable alkanes containing very long carbon–carbon bonds
AA Fokin, LV Chernish, PA Gunchenko, EY Tikhonchuk, H Hausmann, ...
Journal of the American Chemical Society 134 (33), 13641-13650, 2012
Metal‐free, selective alkane functionalizations
AA Fokin, PR Schreiner
Advanced Synthesis & Catalysis 345 (9‐10), 1035-1052, 2003
Functionalized nanodiamonds part I. An experimental assessment of diamantane and computational predictions for higher diamondoids
AA Fokin, BA Tkachenko, PA Gunchenko, DV Gusev, PR Schreiner
Chemistry–A European Journal 11 (23), 7091-7101, 2005
Diamondoids: functionalization and subsequent applications of perfectly defined molecular cage hydrocarbons
MA Gunawan, JC Hierso, D Poinsot, AA Fokin, NA Fokina, BA Tkachenko, ...
New Journal of Chemistry 38 (1), 28-41, 2014
From Dodecahedrapentaene to the “[n]Trannulenes”. A New In-Plane Aromatic Family
AA Fokin, H Jiao, PR Schleyer
Journal of the American Chemical Society 120 (36), 9364-9365, 1998
Functionalized nanodiamonds: Triamantane and [121] tetramantane
PR Schreiner, NA Fokina, BA Tkachenko, H Hausmann, M Serafin, ...
The Journal of organic chemistry 71 (18), 6709-6720, 2006
Substituent effects on the Bergman cyclization of (Z)‐1,5‐hexadiyne‐3‐enes: a systematic computational study
M Prall, A Wittkopp, AA Fokin, PR Schreiner
Journal of Computational Chemistry 22 (13), 1605-1614, 2001
Band gap tuning in nanodiamonds: first principle computational studies
AA Fokin, PR Schreiner
Molecular Physics 107 (8-12), 823-830, 2009
Functionalized nanodiamonds part 3: thiolation of tertiary/bridgehead alcohols
BA Tkachenko, NA Fokina, LV Chernish, JEP Dahl, S Liu, RMK Carlson, ...
Organic letters 8 (9), 1767-1770, 2006
Selective C–H Activation of Aliphatic Hydrocarbons under Phase‐Transfer Conditions
PR Schreiner, O Lauenstein, IV Kolomitsyn, S Nadi, AA Fokin
Angewandte Chemie International Edition 37 (13‐14), 1895-1897, 1998
Origin of the monochromatic photoemission peak in diamondoid monolayers
WA Clay, Z Liu, W Yang, JD Fabbri, JE Dahl, RMK Carlson, Y Sun, ...
Nano letters 9 (1), 57-61, 2009
σ/σ-and π/π-interactions are equally important: multilayered graphanes
AA Fokin, D Gerbig, PR Schreiner
Journal of the American Chemical Society 133 (50), 20036-20039, 2011
Negative-electron-affinity diamondoid monolayers as high-brilliance source for ultrashort electron pulses
S Roth, D Leuenberger, J Osterwalder, JE Dahl, RMK Carlson, ...
Chemical Physics Letters 495 (1-3), 102-108, 2010
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