Electrochemistry of transition metal hydride diphosphine complexes trans-MH(X)(PP)2 and trans-[MH(L)(PP)2]+, M = Fe, Ru, Os; PP = chelating phosphine ligand-Reference-Cited by-同舟云学术

Electrochemistry of transition metal hydride diphosphine complexes trans-MH(X)(PP)2 and trans-[MH(L)(PP)2]+, M = Fe, Ru, Os; PP = chelating phosphine ligand

Published:2021-02 Issue: Volume:516 Page:120124
ISSN:0020-1693
Container-title:Inorganica Chimica Acta
language:en
Short-container-title:Inorganica Chimica Acta

Author:

Drouin Samantha D.,Maltby Patricia A.^ORCID,Rennie Benjamin E.^ORCID,Schweitzer Caroline T.,Golombek Adina^ORCID,Cappellani E. Paul,Morris Robert H.^ORCID

Funder

Discovery grant

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference37 articles.

1. Electrochemical parametrization of metal complex redox potentials, using the ruthenium(III)/ruthenium(II) couple to generate a ligand electrochemical series

2. Ligand additivity effects and periodic trends in the stability and acidity of octahedral .eta.2-dihydrogen complexes of d6 transition metal ions

3. Dihydrogen vs. dihydride. Correlations between electrochemical or UV PES data and force constants for carbonyl or dinitrogen ligands in octahedral, d6 complexes and their use in explaining the behavior of the dihydrogen ligand

4. Stepwise ligand-additivity effects on electrode potentials and charge-transfer spectra in hexahalide, mixed halide/nitrile, and hexakis(nitrile) complexes of ruthenium(IV), -(III), and -(II)

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