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O–H and (CO)N–H bond weakening by coordination to Fe(II)


New N,N’-dimethyl-N,N’-bis(2-pyridylmethyl)-ethane-1,2-diamine derivatives bearing covalently linked OH and (CO)NH groups have been synthesized. The coordination of those pendant hydroxyl/amide groups to a Fe(II) metal center is demonstrated both in solution, even in the presence of chloride as counterion, and in solid state, by means of X-ray diffraction crystal structures. As a result of this coordination, the experimental bond dissociation free energies (BDFE) of O–H and (CO)N–H bonds are remarkably dimished down to 76.0 and 80.5 kcal mol-1, respectively, which is also in agreement with DFT-based theoretical calculations. Those BDFE values are in the range of commonly used hydrogen-atom donor reagents. The strategy presented here allows an unequivocal evaluation of the influence of metal coordination in X–H bond weakening in organic solvents which could be easily extended to other metal centers.

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Publication details

The article was received on 27 Nov 2018, accepted on 10 Jan 2019 and first published on 11 Jan 2019

Article type: Paper
DOI: 10.1039/C8DT04689A
Citation: Dalton Trans., 2019, Accepted Manuscript
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    O–H and (CO)N–H bond weakening by coordination to Fe(II)

    S. Resa, A. Millan, N. Fuentes, L. Crovetto, M. L. Marcos, L. Lezama, D. Choquesillo-Lazarte, V. Blanco, A. G. Campaña, D. J. Cardenas and J. M. Cuerva, Dalton Trans., 2019, Accepted Manuscript , DOI: 10.1039/C8DT04689A

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