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Ar
O
4Bu n H
n
(6.47)
MgBu 2 +
4ArOH
ArO
Mg
Mg
OAr
O
Ar
Me 3 C
where
HOAr
=
HO
CH 3
.
Me 3 C
CF 3
CF 3
F 3 C
In
− 2CpH
2CpIn
+
2
F 3 C
O
O
CF 3
In
F 3 C
CF 3
CF 3
F 3 C
OH
6 . 48
This method has been used to produce a variety of homoleptic aryloxide complexes
and has also been applied to the synthesis of mixed alkyl, aryloxide derivatives of
metals. Partial substitution is typically achieved by simple control of the stoichiometry
or by using sterically demanding aryloxides (Eqs 6.49, 133 , 134
6.50, 135
and 6.51 136 ).
ArO
CH 2 Ph
2PhCH 3
M(CH 2 Ph) 4 +
2ArOH
M
(6.49)
ArO
CH 2 Ph
Me 3 C
where
M = Ti, Zr, Hf; ArOH
=
.
HO
Me 3 C
N
H 3 C
O
2CH 4
H 3 C
(6.50)
2Ga(CH 3 ) 3
+
2
Ga
Ga
CH 3
O
N
CH 3
OH
N
SiMe 3
SiMe 3
R
ArO
R
OAr
4ArOH
Ta
Ta
Ta
Ta
(6.51)
4RH
R
ArO
R
OAr
SiMe 3
SiMe 3
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