Calixarene-based alkynyl-bridged gold(i) isocyanide and phosphine complexes as building motifs for the construction of chemosensors and supramolecular architectures‡
Literature Information
Franky Ka-Wah Hau, Kai-Leung Cheung, Nianyong Zhu, Vivian Wing-Wah Yam
A series of calixarene-based alkynyl-bridged Au(I) isocyanide and phosphine complexes has been designed and synthesized. These complexes are found to exhibit intense emission in dichloromethane solution, in the solid state and in the glass state at 298 K and 77 K. The gold(I) isocyanide complexes with a triazolyl group as a receptor site have been shown to switch on a low-energy emission band upon addition of Zn2+ ions. The new low-energy emission band is ascribed to result from the switching on of the Au⋯Au interaction upon the binding of the Zn2+ ion that gives rise to a reduced HOMO–LUMO energy gap. Furthermore, an interesting supramolecular architecture of tetranuclear gold(I) phosphine stabilized by Au⋯Au interactions has been isolated. Short Au⋯Au distances are found in the X-ray crystal structure.
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Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry












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