The dimethyl-, di-n-butyl-, and diphenyltin(IV) dithiocarbarnate (dtc) complexes [{(RSn)-Sn-2(L-dtc)}(x)] 1-7 (1, L = L1, R = Me; 2, L = U. R = n-Bu; 3, L L2, R Me, x =.; 4, L = L2, R = n-Bu; 5, L = L3, R = Me, x = 2; 6, L = L3, R = n-Bu, x = 2; 7, L L3, R Ph, x = 2) have been prepared from a series of secondary amino acid (AA) homologues as starting materials: N-benzylglycine (alpha-AA derivative = L1), N-benzyl-3-aminopropionic acid (beta-AA derivative = L2), and N-benzyl-4-aminobutyric acid (gamma-AA derivative = L3). The resulting compounds have been characterized by elemental analysis, mass spectrometry, IR and NMR (H-1, C-13, and Sn-119) spectroscopy, thermogravimetric analysis, and X-ray crystallography, showing that in all complexes both functional groups of the heteroleptic ligands are coordinated to the tin atoms. By X-ray diffraction analysis, it could be shown that [{Me2Sn(L-2-dtc)}(x)] (3) is polymeric in the solid state, while the complexes derived from L3 (5-7) have dinuclear 18-membered macrocyclic structures of the composition [{(RSn)-Sn-2(L3-dtc)}(2)]. For the remaining compounds, it could not be established with certainty whether the structures are macrocyclic or polymeric. A theoretical investigation at the B3LYP/SBKJC(d,p) level of theory indicated that the alpha-AA-dtc complexes might have trinuclear macrocyclic structures. The macrocyclic complexes 5-7 have a double-calix-shaped conformation with two cavities large enough for the inclusion of aliphatic and aromatic guest molecules. They are self-complementary for the formation of supramolecuar synthons that give rise to 1 D molecular arrangements in the solid state. Preliminary recognition experiments with tetrabutylammonium acetate have shown that the [{(RSn)-Sn-2(L3-dtc)}(2)] macrocycles 6 and 7 might interact simultaneously with anions (AcO-), which coordinate to the tin atoms, and organic cations (TBA(divided by)), which accommodate within the hydrophobic cavity (ion-pair recognition).