Electrical or Photocontrol of the Rotary Motion of a Metallacarborane

Author:

Hawthorne M. Frederick12,Zink Jeffrey I.12,Skelton Johnny M.12,Bayer Michael J.12,Liu Chris12,Livshits Ester12,Baer Roi12,Neuhauser Daniel12

Affiliation:

1. Department of Chemistry and Biochemistry, University of California, Los Angeles, CA, 90095–1569, USA.

2. Department of Chemistry, Hebrew University of Jerusalem, Givat Ram, Jerusalem, Israel.

Abstract

Rotary motion around a molecular axis has been controlled by simple electron transfer processes and by photoexcitation. The basis of the motion is intramolecular rotation of a carborane cage ligand (7,8-dicarbollide) around a nickel axle. The Ni(III) metallacarborane structure is a transoid sandwich with two pairs of carbon vertices reflected through a center of symmetry, but that of the Ni(IV) species is cisoid . The interconversion of the two provides the basis for controlled, rotational, oscillatory motion. The energies of the Ni(III) and Ni(IV) species are calculated as a function of the rotation angle.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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