Crystallization-induced emission enhancement was achieved in metal nanoclusters for the first time.

A new method termed "in situ two-phase ligand exchange" was developed to obtain alloy nanoclusters. With this approach, a series of alloy nanoclusters were obtained for the first time, including AuAg(SR), AuAg(SR) (x = 4-8), AuCu(SR) (x = 0, 1), and AuCu(SR) (x = 2-5) (R = tert-butyl). Interestingly, single-crystal X-ray crystallography (SC-XRD) shows that their frameworks are all alike except for AuCu(SR) (x = 2-5), indicating that more Cu dopants alter the structure. AuCu(SR) (x = 2-5) exhibits a significantly different configuration. The optical absorption spectra of these bimetal nanoclusters (NCs) show distinct characteristic peaks, indicating that the metal-doping remarkably affects the electronic structure of NCs. The DFT calculations were also employed for determination of NC 1-3 frameworks and understanding their optical properties.

We report the observation of new doping behavior in Au36-xAgx(SR)24 nanoclusters (NCs) with x = 1 to 8. The atomic arrangements of Au and Ag atoms are determined by X-ray crystallography. The new gold-silver bimetallic NCs share the same framework as that of the homogold counterpart, i.e. possessing an fcc-type Au28 kernel, four dimeric AuAg(SR)3 staple motifs and twelve simple bridging SR ligands. Interestingly, all the Ag dopants in the Au36-xAgx(SR)24 NCs are selectively incorporated into the surface motifs, which is in contrast to the previously reported Au-Ag alloy structures with the Ag dopants preferentially displacing the core gold atoms. This distinct doping behavior implies that the previous assignments of an fcc Au28 core with four dimers and 12 bridging thiolates for Au36(SR)24 are more justified than other assignments of core vs. surface motifs. The UV-Vis adsorption spectrum of Au36-xAgx(SR)24 is almost the same as that of Au36(SR)24, indicating that the Ag dopants in the motifs do not change the optical properties. The similar UV-Vis spectra are further confirmed by TD-DFT calculations. DFT also reveals that the energies of the HOMO and LUMO of the motif-doped AuAg alloy NC are comparable to those of the homogold Au36 NC, indicating that the electronic structure is not disturbed by the motif Ag dopants. Overall, this study reveals a new silver-doping mode in alloy NCs.

A gold nanocluster Au17Cd2(PNP)2(SR)12 (PNP=2,6‐bis(diphenylphosphinomethyl)pyridine, SR=4‐MeOPhS) consisting of an icosahedral Au13 kernel, two Au2CdS6 staple motifs, and two PNP pincer ligands has been designed, synthesized and well characterized. This cadmium and PNP pincer ligand co‐modified gold nanocluster showed high catalytic efficiency in the KA2 reaction, featuring high TON, mild reaction conditions, broad substrate scope as well as catalyst recyclability. Comparison of the catalytic performance between Au17Cd2(PNP)2(SR)12 and the structurally similar single cadmium (or PNP) modified gold nanoclusters demonstrates that the co‐existence of the cadmium and PNP on the surface is crucial for the high catalytic activity of the gold nanocluster. This work would be enlightening for developing efficient catalysts for cascade reactions and discovering the catalytic potential of metal nanoclusters in organic transformations.

A Au4Ni2 nanocluster containing a square-planar [-PPh2-Au-S-Au-]2 ring and two nickel-pincer arms is reported here. Abundant intra- and inter-cluster noncolvalent interactions promote the assembly of the nanocluster into a porous...