Abstract
AbstractTwo pure silver nanoparticles (Ag210(iPrPhS)71(Ph3P)5Cl and Ag211(iPrPhS)71(Ph3P)6Cl labeled as SD/Ag210 and SD/Ag211 (SD=SunDi), were found to co‐crystallize in forming compound 1. Single‐crystal X‐ray diffraction (SCXRD) revealed that they differ by only one Ag(PPh3). Their four‐shell nanoparticles consist of three pure Ag metal shells (Ag19@Ag52@Ag45) shielded by a silver‐organic Ag89(iPrPhS)71Cl[Ag(Ph3P)]n outermost shell. The number (n) of Ag(Ph3P) is five for SD/Ag210 and six for SD/Ag211. The pseudo‐fivefold symmetric Ag nanoparticles exhibit surface plasmon absorption similar to a true metallic state but at the nanoscale. This work exemplifies the important effects of phosphine in stabilizing large silver nanoparticles; and offers a platform to investigate the origin of differences in nanoscale metal materials, even differing by only one metal atom; it also sheds light on the regioselective binding of auxiliary Ph3P on the surface of silver nanoparticles.
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