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Xiaolong Zheng Mingzhu Liu Mingxin He Prof. David J. Pine Prof. Marcus Weck 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2017,129(20):5599-5603
A facile method to synthesize shape-shifting patchy particles on the colloidal scale is described. The design is based on the solvent-induced shifting of the patch shape between concave and convex features. The initial concave patchy particles were synthesized in a water suspension by a swelling-induced buckling process. Upon exposure to different solvents, the patches were tuned reversibly to be either concave or convex. These particles can be assembled into chained, branched, zigzag, and cyclic colloidal superstructures in a highly site-specific manner by surface–liquid capillary bridging. The biphasic nature of the particles also enables site-selective surface functionalization. 相似文献
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Marconi N. Peas‐Defrutos Camino Bartolom Max García‐Melchor Pablo Espinet 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(11):3539-3543
By combining kinetic experiments, theoretical calculations, and microkinetic modeling, we show that Pf/Rf (C6F5/C6Cl2F3) exchange between [AuPf(AsPh3)] and trans‐[RhRf(CO)(AsPh3)2] does not occur by typical concerted Pf/Rf transmetalation via electron‐deficient double bridges. Instead, it involves asymmetric oxidative insertion of the RhI complex into the (Ph3As)Au?Pf bond to produce a [(Ph3As)Au?RhPfRf(CO)(AsPh3)2] intermediate, followed by isomerization and reductive elimination of [AuRf(AsPh3)]. Interesting differences were found between the LAu?Ar asymmetric oxidative insertion and the classical oxidative addition process of H2 to Vaska complexes. 相似文献