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Organometallic complexes, spin equilibria

The left-hand dicarbonyl complex is a singlet, whereas the monocarbonyl derivative is a triplet, so the process is clearly spin-forbidden. Despite this, the authors observed the equilibrium between the two to be rapid, and they concluded It seems thus implausible that changes in spin state should slow organometallic transformations as a general rule. ... [Pg.292]

See other pages where Organometallic complexes, spin equilibria is mentioned: [Pg.44]    [Pg.1233]    [Pg.463]    [Pg.3587]    [Pg.1233]    [Pg.4687]    [Pg.52]    [Pg.96]    [Pg.281]    [Pg.140]   
See also in sourсe #XX -- [ Pg.44 ]



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