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A series of substituted-naphthalene complexes have been synthesized of the form [Os(NH 3 ) 5 (η 2 -L)](OTf) 2 (where L = 1-methylnaphthalene, 2-methylnaphthalene, 2-methoxynaphthalene, 2-hydroxynaphthalene, 1-methoxynaphthalene, 1-hydroxynaphthalene, 1-acetonaphthone, 2-acetonaphthone, and phenanthrene), with two or more linkage isomers identified for several of these complexes. The ratio of these isomers changes over time in solution (acetone- d 6 ) and eventually reaches dynamic equilibrium. The final equilibrium ratios and the associated specific rates are reported. In several cases, protonation of an isomer mixture generates a single naphthalenium species, which upon deprotonation provides the original η 2 -naphthalene complex as a single set of ring isomers.
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Winemiller et al. (1997) studied this question.
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