Issue 15, 2019

Evaluation of attractive interactions in the second coordination sphere of iron complexes containing pendant amines

Abstract

The interactions between pendant amines in the second coordination sphere and ligands in the first coordination sphere are important for understanding the structures and reactivity of complexes containing PR2NR′2 ligands, which have been shown to be highly active H2 oxidation/production catalysts. A series of [Fe(PPh2NBn2)2(X)(Y)]n+ complexes have been prepared and structurally characterized. These complexes have two different ligands with which the pendant amines of the diphosphine ligand can interact. The solid state structure of cis-Fe(PPh2NBn2)2Cl2 reveals that the six-membered rings adjacent to the P atoms are in a boat confirmation, resulting in close N⋯P distances that suggests the P atoms have a greater affinity for the lone pair of electrons on the N atom than chloride ligands. Similarly, boat conformations are observed for both rings adjacent to the hydride ligands of trans-[HFe(PPh2NBn2)2(CH3CN)]+ and trans-HFe(PPh2NBn2)2Cl, resulting in short N⋯H distances. Spectroscopic and computational studies of trans-[HFe(PPh2NBn2)2(CO)]+, trans-[HFe(PPh2NBn2)(PPh2NBn2H)(CO)]2+, and trans-[HFe(PPh2NBn2)2(H2)]+ indicate the complexes are more stable when the pendant amines in boat conformations are adjacent to the hydride ligand. These data suggest an attractor ordering of H > CO > H2 > PR3 > Cl ∼ CH3CN.

Graphical abstract: Evaluation of attractive interactions in the second coordination sphere of iron complexes containing pendant amines

Supplementary files

Article information

Article type
Paper
Submitted
16 Cʼhwe. 2019
Accepted
12 Meur. 2019
First published
15 Meur. 2019

Dalton Trans., 2019,48, 4867-4878

Author version available

Evaluation of attractive interactions in the second coordination sphere of iron complexes containing pendant amines

Q. Liao, T. Liu, S. I. Johnson, C. M. Klug, E. S. Wiedner, R. Morris Bullock and D. L. DuBois, Dalton Trans., 2019, 48, 4867 DOI: 10.1039/C9DT00708C

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