Issue 35, 2015

As-stereogenic C2-symmetric organoarsines: synthesis and enantioselective self-assembly into a dinuclear triple-stranded helicate with copper iodide

Abstract

As-stereogenic C2-symmetric 2,5-diaryl-cis-1,4-dihydro-1,4-diarsinines (2,5-diaryl-cis-DHDAs) were synthesized without volatile precursors. A racemic mixture of the ligands enantioselectively self-assembled into a dinuclear triple-stranded helicate with copper iodide in quantitative yield. In the helicate, two metals were bridged via three enantiomerically pure ligands.

Graphical abstract: As-stereogenic C2-symmetric organoarsines: synthesis and enantioselective self-assembly into a dinuclear triple-stranded helicate with copper iodide

Supplementary files

Article information

Article type
Communication
Submitted
20 Apr 2015
Accepted
08 Jun 2015
First published
08 Jun 2015

Dalton Trans., 2015,44, 15372-15376

As-stereogenic C2-symmetric organoarsines: synthesis and enantioselective self-assembly into a dinuclear triple-stranded helicate with copper iodide

H. Adachi, H. Imoto, S. Watase, K. Matsukawa and K. Naka, Dalton Trans., 2015, 44, 15372 DOI: 10.1039/C5DT01490E

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