Reactions of silver(I) perchlorate with the nonplanar aromatic compounds tr
iptycene (L-1), 9,9-bifluorenylidene (L-2), (R)-(+)-1,1-bi-2-naphthol (L-3)
and 2,5-norbornadiene (L-4) have isolated four novel hydrocarbon-bridged p
olymeric complexes: [Ag-3(L-1)(3)(ClO4)(3)]. 2C(6)H(5)Me (1), [Ag-2(L-2)(2)
(ClO4)(2)]. C6H4Me2 (2), [Ag-2(L-3)(C6H6)(2)(ClO4)(2)] (3), and [Ag(L-4)(Cl
O4)] (4). Structural studies using single-crystal X-ray diffraction have sh
own that all compounds contain extended two- or three-dimensional structure
s based on cation-rr interactions. While complex 1 in the solid stale conta
ins a three-dimensional architecture in which die triangular molecule tript
ycene exhibits an unprecedented mu-eta(2)-eta(2) or mu-eta(2)-eta(2)-eta(1)
coordination mode depending on the steric requirements of the network, 3 r
epresents the first example of pi coordination of naphthol-containing micro
pores in its metal complexes. Infinite chains consisting of alternating sil
ver ions and hydrocarbon molecules observed in both 2 and 4 are linked toge
ther by perchlorates, affording 2-D frameworks. The potential use of these
pi complexes for the rational control and synthesis of polymeric organometa
llic materials is discussed. Crystal data: 1, C74H58Ag3Cl3O12, monoclinic,
Cc, a = 37.951(4) Angstrom, b = 8.047(4) Angstrom, c = 20.882(5) Angstrom,
beta = 93.72(1)degrees, V= 6365(3) Angstrom(3), Z = 4; 2, C60H42Ag2Cl2O8. m
onoclinic, P2(1)/n, a = 12.317(4) Angstrom, b = 7.961(1) Angstrom, c = 24.7
41(1) Angstrom, beta = 100.015(1)degrees, V = 2389(6) Angstrom(3) , Z = 2;
3, C32H26Ag2Cl2O10, tetragonal, P4(1)2(1)2, a = 8.759(6) Angstrom, c = 39.9
67(8) Angstrom V= 3065(3) Angstrom(3), Z = 4; 4, C7H8-AgClO4 monoclinic, p2
(1)/n, a = 9.847(4) Angstrom, b = 9.0543 Angstrom, c = 10.662(3) Angstrom,
beta = 106.72(2)degrees, V= 910.3(4) Angstrom(3), Z = 4.