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Monofunctional bidentate
OH
R
O
H
O
H
R
HC
N
N
HC
H
R′
R
′′
′′′
N
(R
′ =
alkyl or aryl)
HsalNR
Me, Bu t , Ph, CF 3
(R
′ =
R
′′ =
R
R
, R
′′ =
Me, CF 3 ; Me, Ph;
(a)
(b)
R
′′′
=
alkyl or aryl)
(c)
Bifunctional tridentate
OH
OH
HO
C
NR
′′
OH
CN
R
R
(R
′ =
H or Me; R
′′ =
C 2 H 4 , CH 2 CHMe)
(R
′ =
H or Me)
(e)
(d)
Bifunctional tetradentate
OH
OH
HC
N
N
CH
B
(B = CH 2 CH 2 (salen H 2 ), CH 2 CHMe
(salpnH 2 ), o -C 6 H 4 (salphen H 2 ))
(f)
R
R
O
O
H
H
N
N
B
R′′
R
′′
Me, Bu t , Ph, CF 3 ;
(R
′ =
R
′′ =
R
, R
′′ =
Me, CF 3 ; Me, Ph;
B
=
CH 2 CH 2 , CH 2 CHMe, C 6 H 4 )
(g)
Figure 2.15 Some of the types of mono- and bi-functional bi- and
tri-dentate Schiff bases and ˇ -ketoamines whose reactions with metal
alkoxides have been investigated.
Another noteworthy feature is that homoleptic derivatives of a wide variety of mono-
functional bidentate Schiff bases and ˇ -ketoamines with a number of metals (Nb, Ta,
Al, Sb) may be prepared by the alkoxide route. However, attempted preparations of
analogous derivatives of Ti and Zr have not been successful.
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