Synthesis, spectra, crystal structures and anticancer studies of 26‐membered macrocyclic dibutyltin(IV) dithiocarbamate complexes: Single‐source precursors for tin sulfide nanoparticles

Four new macrocyclic dinuclear dibutyltin(IV) dithiocarbamate complexes of the type [Bu2Sn(dtc)]2, where dtc = hexane‐1,6‐diylbis(4‐fluorobenzyldithiocarbamate) anion (1), hexane‐1,6‐diylbis(4‐chlorobenzyldithiocarbamate) anion (2), hexane‐1,6‐diylbis(furfuryldithiocarbamate) anion (3) and hexane‐1,6‐diylbis(pyrrole‐2‐ylmethyldithiocarbamate) anion (4), have been prepared. The dithiocarbamate ligands efficiently self‐assemble with Bu2Sn(IV) to form bimetallic 26‐membered macrocycles. All the complexes have been characterized using elemental analysis, infrared and NMR (1H and 13C) spectroscopies and X‐ray crystallography. Single‐crystal X‐ray diffraction analysis of all the complexes confirms the formation of the dinuclear metallomacrocycles in which dithiocarbamate ligands are asymmetrically bound to the tin atoms. The coordination sphere around the tin atom in 1–4 can be described as a skew trapezoidal bipyramid. The dimensions of the cavity of the macrocycles of 1–4 are ca 8.0 × 9.0 Å2. Complexes 1–4 were evaluated for their in vitro anticancer activity against MCF‐7 and HL‐60 cells. Complexes 1 and 2 are more active against MCF‐7 and HL‐60. Thermal decomposition of 1 and 4 yielded tin sulfides. They were characterized using powder X‐ray diffraction (PXRD), high‐resolution transmission electron microscopy and UV diffuse reflectance and energy‐dispersive X‐ray spectroscopies. PXRD studies reveal that the as‐prepared tin sulfides are composed of orthorhombic phase of SnS. Four new macrocyclic dinuclear dibutyltin(IV) dithiocarbamate complexes of the type [Bu2Sn(dtc)]2 have been prepared. The coordination sphere around the tin atom in all the complexes can be described as a skew trapezoidal bipyramid. The dimensions of the cavity of the macrocycles are ca 8.0 × 9.0 Å2. All the complexes were evaluated for their in vitro anticancer activity against MCF‐7 and HL‐60 cells. Thermal decomposition of the complexes yielded tin sulfide nanoparticles.