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ORIGINAL PAPER Li‐Ying Sun Corresponding Author sunxlx@outlook.com Intensive Care Unit, Beijing Friendship Hospital, Capital Medical University, Beijing, China Correspondence Li‐Ying Sun, Intensive Care Unit, Beijing Friendship Hospital, Capital Medical University, 95 Yong‐an Road, Beijing, 100050, China.
The full text of this article hosted at iucr.org is unavailable due to technical difficulties. Communication Supramolecular Control of Photocycloadditions in Solution: In Situ Stereoselective Synthesis and Release of Cyclobutanes Li‐Li Ma Key Laboratory of Synthetic and Natural Functional Molecule Chemistry, College of Chemistry and Materials Science, Northwest University, Xi'an, 710127 P. R. China These authors contributed equally to this work.
A procedure for the synthesis of three‐dimensional hexakisimidazolium cage compounds has been developed. The reaction of the trigonal trisimidazolium salts H L(PF ) , decorated with three N‐olefinic pendants, and silver oxide yielded trinuclear trisilver(I) hexacarbene molecular cylinders of the type [Ag L ]3+ with the olefinic pendants from the two different tricarbene ligands arranged in three pairs.
A procedure for the synthesis of three‐dimensional hexakisimidazolium cage compounds has been developed. The reaction of the trigonal trisimidazolium salts H L(PF ) , decorated with three N‐olefinic pendants, and silver oxide yielded trinuclear trisilver(I) hexacarbene molecular cylinders of the type [Ag L ]3+ with the olefinic pendants from the two different tricarbene ligands arranged in three pairs.
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