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Self-assembled Transition Metal Coordination Frameworks of ...

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" F<br />

Ligands<br />

A indicates a typical double-bond nature and the ketone form. The N—N and C—N<br />

bond lengths (Table 2.7) <strong>of</strong> the carbohydrazone core group are comparable to the<br />

corresponding lengths in bis(methyl 2-pyridyl ketone) carbohydrazone [9], indicate<br />

some electron delocalization in the<br />

'<br />

N(3)/N (4)/C(12)/N<br />

08<br />

(5)/N (6) moiety.<br />

9J<br />

@022 ( C23 O1<br />

~ ' ~ N2<br />

. . C9<br />

C21 3 N5 (:13 Cf C10 N6 ' C12 i N4 , cs \ N3 - 'l;.<br />

czo‘ C19 <<br />

*~ 4<br />

I<br />

v<br />

x.<br />

C11<br />

N7 Q‘ C14 N1 ._ - C5<br />

1' 015 C‘ s C4<br />

C18. \..<br />

Q _ 0<br />

917 # Q C16 c2 _. cab<br />

Fig. 2.18. The molecular stmcture <strong>of</strong> 1~12L4, with 50% probability displacement<br />

ellipsoids and the atom numbering scheme. H atoms are shown as small spheres <strong>of</strong><br />

arbitrary radii.<br />

Table 2.7. Selected bond lengths (A) and angles (°) <strong>of</strong> HQL4.<br />

0(1)-c(12)<br />

N(3)—C(6)<br />

N(3)—N(4)<br />

N(4)-C(12)<br />

N(5)—N(6)<br />

N(5)-C(12)<br />

N(6)—C(l3)<br />

C(5)-C(6)<br />

c(6)-c(7)<br />

C(l3)—C(l9)<br />

C(13)—C(14)<br />

1.2ll6(18)<br />

1.2945 (19)<br />

1.3662 (17)<br />

1.367 (2)<br />

1.3556 (17)<br />

1.3799 (19)<br />

1.2950 (18)<br />

1.489 (2)<br />

1.4903 (19)<br />

1.482 (2)<br />

1.493 (2)<br />

N(3)-C(6)-C(5<br />

N(3)—C(6)—C(7<br />

0(1)-C(12)-N(4<br />

N(4)—C(l2)-N(5<br />

N(6)-C(13)-C(l9<br />

N(6)-C(l3)—C(l4<br />

C(7)—C(6)—C(5<br />

0(1)-C(12)-N(5<br />

C(19)-C(13)-C(14)<br />

128.10 (13)<br />

112.55 (13)<br />

125.56 (14)<br />

113.51 (13)<br />

128.00 (13)<br />

113.27 (12)<br />

119.35(13)<br />

l20.93(15)<br />

l18.70(12)<br />

65

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