Modern bottom-up synthesis to nanocrystalline solid-state materials often lacks the reasoned product control that molecular chemistry boasts from having over a century of research and development. In this study, six transition metals including iron, cobalt, nickel, ruthenium, palladium, and platinum were reacted with the mild reagent didodecyl ditelluride in their acetylacetonate, chloride, bromide, iodide, and triflate salts. This systematic analysis demonstrates how rationally matching the reactivity of metal salts to the telluride precursor is necessary for the successful production of metal tellurides. The trends in reactivity suggest that radical stability is the better predictor of metal salt reactivity than hard–soft acid–base theory. Of the six transition-metal tellurides, the first colloidal syntheses of iron and ruthenium tellurides (FeTe2 and RuTe2) are reported.

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