The synthesis and crystal structure of the complex formed by the all-cis ep
imer of C-methylcalix[4]resorcinarene (1) and triethylammonium nitrate are
reported. "1(HNEt3+)(4) . (NO3-)(4)(2)", crystallizes in the monoclinic spa
ce group P2(1)/n, a=25.796(2), b= 16.6048(11), c=29.5659(10) Angstrom, beta
=94.636(4)degrees, V= 12623(2) Angstrom(3), Z= 8. Refinement led to a final
conventional R-1 value of 0.128 for 12428 reflections and 1473 parameters.
The resorcinarene displays the usual bowl-type shape, with four hydroxyl p
rotons involved in intramolecular hydrogen bonds, whereas the remaining fou
r make hydrogen bonds with four bridging nitrate ions, which results in the
formation of infinite chains. Those chains are arranged so as to form laye
rs, between which the triethylammonium ions and the remaining nitrate ions
are hydrogen-bonded one to another.