“…Since the trans influence of the halogen ligand is much smaller than that of the dithiocarbamate ligand, the Te--Sax bond is stronger than all the Te--Seq bonds. This situation is realized in complexes of the general formula Te(R1RzNCS2)3C1 with R 1 = R 2 = Et [as the 1:1 dioxane solvate, (6)] (von Deuten, Schnabel & Klar, 1980), R 1 = R 2 = CH2CH2OH [as the dihydrate, (7)] (Rao, Seshasayee, Aravamudan & Radha, 1983) and R 1 = Me, R 2 = CHECH2OH [as the dihydrate, (8)] (Husebye & Thowsen, 1981), where there is strengthened axial coordination (Te~S 2.465-2.512,~, trans C1--Te~S angle 174.9-179.1 °) and significantly weakened equatorial coordination (Te~S 2.801-2.874 A, cis angle 108.3-114.1°). The structure of the Br analogue of (8), compound (9), is practically the same (Husebye, 1979).…”