The As-pi interaction, in conjunction with reversible As-thiolate bond formation, is used to direct the self-assembly of dinuclear As2L2Cl2 (L = a dithiolate) macrocycles that exist as equilibrium mixtures of both syn and anti diastereomers. The diastereomeric excess of these self-assembly reactions is controlled in a predictable manner by prudent choice of different achiral, isomeric ligands. A general method for the preparation of AS(2)L(2)Cl(2) macrocycles is established, and strategies to control the diastereoselective self-assembly of regioisomeric macrocycles in solution and the crystalline state are described. A mechanism for the interconversion between diastereomers (a slow process on the NMR time scale) is suggested, and variable-temperature NMR spectroscopic data show that the diastereomeric excess (de) decreases with increasing temperature. anti-As-2(L-2,L-6)(2)Cl-2 crystallizes in monoclinic space group P2(1)/n with a = 6.3949(13), b = 19.675(4), c 10.967(2) A, = 106.817(3)degrees, and Z = 2. anti-AS(2)(L-1,L-5)(2)Cl-2 crystallizes in monoclinic space group P2(1)/c with a 6.813(4), b 19.085(12), c = 10.277(6) A, = 107.788(10)0, and Z = 4. syn-AS(2)(L-1,L-4)(2)Cl-2-CHCl3 crystallizes in triclinic space group P1 with a = 19.313(4), b = 19.923(4), c = 24.508(5) A, alpha = 78.110(4)degrees, beta = 78.860(5)degrees, 89.183(5)degrees, and Z = 12. AS(2) (L-1,L-4)(2)Cl-2 center dot C6H6 crystallizes in monoclinic space group P211n with a = 10.3332(7), b = 34.375(2), c 17.8593(12) A,beta= 98.9650(10)degrees, and Z = 8.