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Two donor/acceptor complexes between halide anion donors and the tetraiodothiophene acceptor with tetra(n-butyl)ammonium countercations, {(H9C4)4N⊕X⊖···(IC)4Sg (X⊖ = I⊖, SCN⊖) could be crystallized from acetone solutions of the components R4N⊕X$ and (IC)4S by using low-gradient techniques. Low temperature structural studies revealed that the molecule packing motifs are layers of halide anion/tetraiodothiophene patterns penetrated each by one of the four R4N⊕ n-butyl chains. The structure discussion emphasizes observed regularities such as the preferred coordination X⊖···I by the polyiodo acceptor molecules to dimers, followed by the additional aggregation to layers and the inclusion of one n-butyl chain fromeach voluminous R4N⊕ countercation. Especially this effect could be an essential crystallization principle for the fascinating self-assembly comprising a halide anion and a polyiodo acceptor molecule.
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Bock et al. (2002) studied this question.
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