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. Author manuscript; available in PMC: 2010 Jun 3.
Published in final edited form as: J Am Chem Soc. 2009 Jun 3;131(21):7402–7410. doi: 10.1021/ja900766b

Figure 7.

Figure 7

Different stereoelectronic environments experienced by the buried methyl groups of 2 and 6 bound within 1. The methyl group directed towards the cavitand wall (equatorial, in red) only experiences the anisotropic shielding of a single aromatic ring at a given time whiles the one deep in the cavity (axial, blue) experiences the effects of the four aromatics of the resorcinarene cone (NMR shifts expressed in ppm).