In situ electrochemical synthesis of Ni(I) complexes with aminomethylphosphines as intermediates for hydrogen evolution

[Display omitted] Nickel (I) complexes of 1,5-diaza-3,7-diphosphacyclooctane PPh2NR2 ligands were obtained from precursor Ni(II) by exhaustive electrolysis of [Ni(PPh2NR2)2]2+ precursors at the Ni(II/I) couple potential and characterized by several techniques. Paramagnetic Ni(I) complexes were inves...

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Bibliographic Details
Published in:Electrochimica acta 2017-01, Vol.225, p.467-472
Main Authors: Khrizanforova, V.V., Morozov, V.I., Strelnik, A.G., Spiridonova, Yu. S., Khrizanforov, M.N., Burganov, T.I., Katsyuba, S.A., Latypov, Sh. K., Kadirov, M.K., Karasik, A.A., Sinyashin, O.G., Budnikova, Y.H.
Format: Article
Language:English
Subjects:
Catalysis
Coordination compounds
Electrolysis
Electrolytes
ESR
Hydrogen
Hydrogen evolution
Nickel
spectroelecrtochemistry
Spectrum analysis
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Summary:[Display omitted] Nickel (I) complexes of 1,5-diaza-3,7-diphosphacyclooctane PPh2NR2 ligands were obtained from precursor Ni(II) by exhaustive electrolysis of [Ni(PPh2NR2)2]2+ precursors at the Ni(II/I) couple potential and characterized by several techniques. Paramagnetic Ni(I) complexes were investigated by cyclic voltammetry, spectroelectrochemistry UV/Vis and ESR methods at room temperature and in a frozen solution. Catalytic behavior of Ni(I) complex in different ligand environment for hydrogen evolution from acid depends from the ligand nature. The two possible catalytic cycles were proposed depending on the nitrogen substituents in 1,5-diaza-3,7-diphosphacyclooctane.
ISSN:0013-4686
1873-3859
DOI:10.1016/j.electacta.2016.12.081