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2 Homometallic Alkoxides

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Metal Aryloxides 455<br />

2Ln C 3Hg⊲C6F5⊳2 C 6HOAr ! 2[Ln⊲OAr⊳3] C 3Hg C 6C6H5F ⊲6.12⊳<br />

where Ln = Nd, Er, Sm, Yb, Lu; HOAr = HO .<br />

where ArO = O<br />

.<br />

Ph<br />

Ph<br />

Yb C 2TlOAr THF<br />

! [Yb⊲OAr⊳2⊲THF⊳3] C 2Tl ⊲6.13⊳<br />

Me 3C<br />

Me3C<br />

CH 3<br />

3.2 From Aqueous or Protic Solutions of Salts<br />

The synthesis of many metal derivatives of complexing agents such as 8hydroxyquinoline<br />

and salicylaldehyde oxime begins with aqueous solutions of metal<br />

ions (e.g. sulfates, nitrates, etc.). Addition of the ligand and suitable control of pH<br />

allows either precipitation of the coordination compound or its extraction into nonprotic<br />

media for either qualitative determination or work up (Eqs 6.14 93 and 6.15 94 ).<br />

where HOAr = .<br />

N<br />

OH<br />

Al 3C ⊲aq⊳ C 3HOAr Base<br />

! [Al⊲OAr⊳3] ⊲6.14⊳<br />

BeSO4.4H2O + O O O<br />

(6.15)<br />

OH OH<br />

Be<br />

H2O The synthesis of metal derivatives of strongly acidic phenols such as 2,4,6trinitrophenol<br />

(picric acid) and 2,4-dinitrophenol (Eq. 6.16 95 ) is typically carried out<br />

in the presence of water or other protic solvents such as acetone/alcohol mixtures.<br />

O<br />

OH 2<br />

Ca 2C ⊲aq⊳ C 2HOAr NaOH<br />

! Ca⊲OAr⊳2.7H2O ⊲6.16⊳

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