Constructing magnetic molecular solids by employing three-atom ligands as bridges

Ammonium thiocyanate (NH4SCN) is introduced to exchange the long, insulating ligands used in colloidal nanocrystal (NC) synthesis. The short, air-stable, environmentally benign thiocyanate ligand electrostatically stabilizes a variety of semiconductor and metallic NCs in polar solvents, allowing solution-based deposition of NCs into thin-film NC solids. NH4SCN is also effective in replacing ligands on NCs after their assembly into the solid state. The spectroscopic properties of this ligand provide unprecedented insight into the chemical and electronic nature of the surface of the NCs. Spectra indicate that the thiocyanate binds to metal sites on the NC surface and is sensitive to atom type and NC surface charge. The short, thiocyanate ligand gives rise to significantly enhanced electronic coupling between NCs as evidenced by large bathochromic shifts in the absorption spectra of CdSe and CdTe NC thin films and by conductivities as high as (2 ± 0.7) × 103 Ω–1 cm–1 for Au NC thin films deposited from solut...

Thiocyanate-Capped Nanocrystal Colloids: Vibrational Reporter of Surface Chemistry and Solution-Based Route to Enhanced Coupling in Nanocrystal Solids

Rhodium(II) carboxylates

Structural, antimicrobial and spectral studies of copper(II) complexes of 2-benzoylpyridine N(4)-phenyl thiosemicarbazone

We report the synthesis and characterization of gold core palladium shell (Au@Pd) nanoparticles with thickness-controlled shell as an improved transition-metal substrate for surface-enhanced Raman scattering (SERS). By changing the molar ratio of H2PdCl4 to Au, the Pd shell thickness can be precisely controlled from a few nanometers down to ca. one monolayer. A series of characterizations were performed using transmission electron microscopy (TEM), UV−vis, SERS, and electrochemical techniques. The results confirmed the core−shell structure and the uniform and pinhole-free nature of the Pd shell, ensuring the properties of Pd without possible interference from Au. Consistent with theoretical prediction, the core−shell setting borrows high SERS activity from the Au core through the long-range electromagnetic enhancement in addition to the enhancement from the Pd shell itself. Moreover, their SERS activity can be optimized by the tunable shell thickness and core size. The nm-Au@Pd/Pd electrodes allow us to o...

R.A. Bailey

Papers

Infrared spectra of complexes of the thiocyanate and related ions