Issue 93, 2015

Charge control of the inverse trans-influence

Abstract

The synthesis and characterization of uranium(VI) mono(imido) complexes, by the oxidation of corresponding uranium(V) species, are presented. These experimental results, paired with DFT analyses, allow for the comparison of the electronic structure of uranium(VI) mono(oxo) and mono(imido) ligands within a conserved ligand framework and demonstrate that the magnitude of the ground state stabilization derived from the inverse trans-influence (ITI) is governed by the relative charge localization on the multiply bonded atom or group.

Graphical abstract: Charge control of the inverse trans-influence

Supplementary files

Article information

Article type
Communication
Submitted
27 Aug 2015
Accepted
25 Sep 2015
First published
25 Sep 2015
This article is Open Access
Creative Commons BY license

Chem. Commun., 2015,51, 16671-16674

Author version available

Charge control of the inverse trans-influence

H. S. La Pierre, M. Rosenzweig, B. Kosog, C. Hauser, F. W. Heinemann, S. T. Liddle and K. Meyer, Chem. Commun., 2015, 51, 16671 DOI: 10.1039/C5CC07211E

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