Abstract

Wurtzite CdSe quantum belts with L-type n-octylamine, L-type ammonia, or Z-type Cd(oleate)2 ligands are exchanged for several metal-dithiocarbamate ligands [M(S2CNR1R2)2]: Cd(S2CNPhMe)2, Cd(S2CNEt2)2, Zn(S2CNPhMe)2, and Zn(S2CNEt2)2. Successful ligand exchange with all M(S2CNR1R2)2 compounds occurs from {CdSe[Cd(oleate)2]0.19} quantum belts (QBs), which induce similar spectral shifts in the absorption spectra of the ligand-exchanged QBs. Spectroscopic data, experimentally determined lattice strains, and ligand exchanges with [Na][Et2NCS2] and [NH4][MePhNCS2] establish that the [M(S2CNR1R2)2] ligands bind as bound-ion-paired X-type ligands with (S2CNR1R2)- groups ligated directly to the QB surfaces and [M(S2CNR1R2)]+ groups serving as the charge-balancing ion-paired countercations. The X-type dithiocarbamate ligands do not impart any special electronic effects to the CdSe QBs.

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