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IV
320
III
240
II
160
I
80
0
0.4
0.8
1.2
1.6
2.0
2.4
M(OPr i )
M
Molar ratio
(OPr i ) 4
Figure 3.3 Titration between
M 0 OPr i 4 and M OPr i . Curve I: (Ž)
NaOPr i M /4.77 vs Zr OPr i 4 . Pr i OH
M /80.49; Curve II: ( ) KOPr i M /9.97
vs Zr OPr i 4 . Pr i OH M /43.011; Curve
III: (ž)NaOPr i M /9.94 vs Ti OPr i 4
M /37.7; Curve IV: (ð) KOPr i
M /9.94
vs Ti OPr i 4 M /37.7.
R
R
R
O
O
RO
OR
RO
M
M
OR
RO
OR
O
Figure 3.4 Schematic
representation
of
a
nona-alkoxodimetal-
late(IV) ligand.
manner 188 that suits their preferred coordination states is remarkable. The possibilities
of the alkoxometallate( IV ) ligands to function as simpler fM OR 5 g and fM OR 6 g 2
also enhance their versatility in a remarkable manner, as revealed by their X-ray
crystal structural studies at an ever-increasing pace since 1984; 217 these have in
general confirmed the conclusions about their plausible structures on the basis of
simpler colligative, spectroscopic, and other physico-chemical studies. A number of
representative examples of these types of tetra-alkoxometallate( IV ) (including a few
heterotermetallic) derivatives are listed in Table 3.4. and an attempt is made in the
following paragraphs to rationalize their structural features (see also Chapter 4).
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