Selenium (Se) substitution drastically increases the transition temperature of iridium ditelluride (IrTe$_{2}$) to a diamagnetic superstructure from 278 K to 560 K. Transmission electron microscopy experiments revealed that this enhancement is accomp
anied by the evolution of non-sinusoidal structure modulations from $q = 1/5(10bar{1})$- to $q = 1/6(10bar{1})$-types. These comprehensive results are consistent with the concept of the destabilization of polymeric Te-Te bonds at the transition, the temperature of which is increased by chemical and hydrostatic pressure and by the substitution of Te with the more electronegative Se. This temperature-induced depolymerization transition in IrTe$_{2}$ is unique in crystalline inorganic solids.
