Fig. 3: Precursor and typical intermediates consisting of larger even- and odd-membered rings. | Nature Communications

Fig. 3: Precursor and typical intermediates consisting of larger even- and odd-membered rings.

From: On-surface synthesis and characterization of anti-aromatic cyclo[12]carbon and cyclo[20]carbon

Fig. 3

a Ia IV C20Cl12. b Ib IV C20Cl9. c Ic IV C20Cl2 with a 10-membered ring. d Id IV C20Cl2 with 8- and 10-membered rings. e Ie IV C20Cl4 with a 9-membered ring. f If IV C20Cl2 with a 13-membered ring. g Ig IV C20Cl2 with a 16-membered ring. Structures (a Ig I), AFM images (a IIg II), AFM simulations (b IIIg III), Laplace-filtered AFM images are shown (b IVg IV). AFM simulations are based on gas-phase DFT-calculated geometries. The scale bar in (a II) applies to all images. Reference set point of Δz for a II to g II: I = 5 pA, V = 0.3 V.

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