Preparations of CdTe quantum platelets, magic-size (CdTe) 13 nanoclusters, and CdTe quantum wires are described using (Me 2 N) 3 PTe (with (Me 2 N) 3 P) as a Te precursor. The (Me 2 N) 3 PTe/(Me 2 N) 3 P precursor mixture is shown to be more reactive than mixtures of trialkylphosphine tellurides and the corresponding trialkylphosphines, R 3 PTe/R 3 P, which are commonly employed in nanocrystal syntheses. For syntheses conducted in primary amine solvents, (Me 2 N) 3 PTe and (Me 2 N) 3 P undergo a transamination reaction, affording (Me 2 N) x (RHN) 3−x PTe and (Me 2 N) x (RHN) 3−x P (R = n-octyl or oleyl). The transaminated (Me 2 N) x (RHN) 3−x PTe derivatives are shown to be the likely Te precursors under those conditions. The enhanced reactivities of the tris(amino)phosphine tellurides are ascribed to increased nucleophilicity due to the amino-N lone pairs.