Electrochemical and EPR spectral studies of mono- and bimetallic (trispyrazolylborato)molybdenum and tungsten complexes with extended di-phenol bridging ligands; evidence for electron exchange below the fast limit
Author:
Publisher
Elsevier BV
Subject
Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry
Reference12 articles.
1. Monometallic, homo- and hetero-bimetallic complexes based on redox-active tris(3,5-dimethylpyrazolyl)borato molybdenum and tungsten nitrosyls. Part 7. Compounds containing strongly interacting redox centres derived from para-substituted anilines and phenols
2. Monometallic, homo- and hetero-bimetallic complexes based on redox-active tris(3,5-dimethylpyrazolyl)borato molybdenum and tungsten nitrosyls. Part 7. Compounds containing strongly interacting redox centres derived from para-substituted anilines and phenols
3. EPR and electrochemical studies of bimetallic seventeen-electron molybdenum species exhibiting unusually large interactions across bipyridyl bridging ligands
4. Metal–metal interactions across symmetrical bipyridyl bridging ligands in binuclear seventeen-electron molybdenum complexes
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2. Redox activity of bimetallic complexes based on tris(3,5-dimethylpyrazolyl)borato molybdenum(II) and tungsten(II) nitrosyls. Complexes derived from ethane-1,2-diol and the crystal structure of anti-[Mo(NO){HB(3,5-Me2C3HN2)3}(OCH2CH2O)]2·4CHCl3;Polyhedron;2007-04
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