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Self-assembled Transition Metal Coordination Frameworks of ...

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Chapter 3<br />

antiferromagnetic coupling. For complex 4 (the temperature dependence curves <strong>of</strong> X,“<br />

and um are shown in Fig. 3.32), however, we could not get a reasonable fit, may be<br />

associated with zero-field splitting (D) especially at lower temperatures and/or due to<br />

slight variations in M—X—M angles, so that more J values need to be considered. The<br />

M—O—M arrangement at 180° is known as an ideal structure for strong<br />

antiferromagnetism [55]. This linearity as the origin <strong>of</strong> strong AF coupling is in<br />

accordance with VB [56-58] and MO [59] studies. Logically, Kahn also explained this<br />

feature in his book [60]. The temperature dependence <strong>of</strong> effective magnetic moment<br />

curves for complexes 1 and 4 are also consistent with these results, though lacks<br />

reasonable fits. We have reported these results recently [61]. The field dependence <strong>of</strong><br />

magnetic susceptibility<br />

6<br />

for these compounds (Fig. 3. 33) not showed any indication <strong>of</strong><br />

ferromagnetic<br />

__<br />

component and is in agreement<br />

/(.1<br />

with overall antiferromagnetism.<br />

8-.<br />

I<br />

;<br />

MiZ 9- '<br />

=: 4 2 - -I‘.-,3‘ ""<br />

I<br />

. * 55' ‘I . _. 1' I"'<br />

g -__||I ‘nu<br />

.10‘<br />

0-.<br />

' I ' I ' I ' I ' I ' I ' I ' I ‘<br />

O 50 100 150 200 250 300 350<br />

T (K)<br />

Fig. 3.29. Temperature dependence <strong>of</strong> effective magnetic moment um (I) for the<br />

complex 1 (the variations are due to poor data collection).<br />

116

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