These authors contributed equally to this work.
Full Paper
Donor-Induced Helical Inversion of 1,1′-Binaphthyl Connecting with Two Molybdenum Complexes
Article first published online: 31 AUG 2012
DOI: 10.1002/chem.201201671
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Ma, L., Jin, R., Bian, Z., Kang, C., Chen, Y., Xu, J. and Gao, L. (2012), Donor-Induced Helical Inversion of 1,1′-Binaphthyl Connecting with Two Molybdenum Complexes. Chem. Eur. J., 18: 13168–13172. doi: 10.1002/chem.201201671
- †
These authors contributed equally to this work.
Publication History
- Issue published online: 27 SEP 2012
- Article first published online: 31 AUG 2012
- Manuscript Received: 12 MAY 2012
Funded by
- National Natural Science Foundation of China. Grant Number: 20502024
- State Key Laboratory of Polymer Physics and Chemistry
Keywords:
- biaryls;
- chirality;
- circular dichroism;
- helical structures;
- molybdenum
Abstract
An atropisomeric biaryl molecule with a given absolute configuration could present two opposite helical conformations through the rotation around C
C single bond. To the best of our knowledge, the biaryl system is the simplest helical inversion model apart from stereomutation between two enantiomers. Herein, we first report such true helical inversion phenomena of biaryl compounds. Two [MoVIO2(L)]-type complexes, in which L is a tridentate dioxoanionic pyridine O,N,O-ligand, are coalesced on the 2,2′,3,3′-positions of an (R)-1,1′-binaphthyl unit and an intramolecular dioxo bridge is formed by two Mo
O⋅⋅⋅Mo interactions. Exterior strong donors can coordinate to molybdenum to interrupt this dioxo bridge and inversions from negative to positive chirality are explicitly observed by circular dichroism spectroscopy, consistent with single-crystal X-ray diffraction analyses.

1521-3765/asset/2111_left.gif?v=1&s=0561086440e3dfc935e925fa17e4b4c8a50bbfe3)
1521-3765/asset/2111_right.gif?v=1&s=9fa3626b72da80da2a89f547de4d2cc5d7fadfe6)
