We report the decomposition of the Pt1Ag24(SPhCl2)18 nanocluster into a crown-like Pt1Ag4(SR)8 (SR = 2,4-SPhCl2 and 4-SPhBr) complex. UV-vis spectra and single crystal X-ray diffraction were used to track the structure-conversion process. Based on the total structure, the differences in ligand exchange rates at different sites and the effects on the stability were mapped out. This work can not only help us understand the ligand exchange behavior of the clusters, but also provide experimental support for the design of stable metal clusters.
Chirality has risen as an attractive topic in materials research in recent years, but the attainment of enantiopure materials remains a major challenge. Herein, we obtained homochiral nanoclusters by a recrystallization strategy, without any chiral factors (i.e., chiral ligands, counterions, etc.). Through the rapid flipping of configuration of silver nanoclusters in solution, the initial racemic Ag40 (triclinic) nanoclusters are converted to homochiral (orthorhombic) as revealed by X-ray crystallography. In the seeded crystallization, one homochiral Ag40 crystal is used as a seed to direct the growth of crystals with specific chirality. Furthermore, enantiopure Ag40 nanoclusters can be used as amplifiers for the detection of chiral carboxylic drugs. This work not only provides chiral conversion and amplification strategies to obtain homochiral nanoclusters but also explains the chirality origin of nanoclusters at the molecular level.
Ligands play an essential role in cluster assembly; however, understanding this behavior at the atomic level is far off. In this work, Cd12Ag32(S-PhOMe)36(PPh)4@Cd6Ag2(S-PhOMe)6Cl6(PPh3)8@Ag6(S-PhOMe)6Cl2 (Abbrev. Cd12Ag32-1) and Cd12Ag32(S-c-C6H11)36 (Abbrev. Cd12Ag32-2) were synthesized and structurally determined by single-crystal X-ray diffraction. An important finding is the selective adsorption of phosphine ligands that is caused by the different types of thiol ligands. In addition, Cd12Ag32-1 follows a unique stacking pattern in a superlattice with multiple inter-cluster channels. Overall, this study is helpful for an in-depth understanding of the effect of mixed ligands on nanocluster formation and the correlation between structure and properties in the nanocluster range.
