Biology Reference
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The
analogous
platinum
[3]catenane
(
BPP34C10
)
-(
M5b
)
2
could be isolated in 70% yield by reaction of
L5
·2PF
,
BPP34C10
,
6
1
and platinum complex (en)Pt(OTf )
H
NMR spectrum showed very similar chemical shifts to those of the
analogous palladium catenane. The electrospray ionization mass
spectrometry supported the structure, showing signals resulting
from the loss of between three and five hexafluorophosphate
anions.
In Fig. 11.11 the crystal structure of catenane
(
in CH
CN at 50
°
C. The
2
3
is presented. The X-ray study revealed a
[3]catenane structure with the metallocycle
DB24C8
)
M5a
·5NO
2
3
M5a
encircled by two
C-shaped
molecules around the methylene groups (red
macrocycles in Fig. 11.11). Two of the catechol rings are inserted
DB24C8
Figure 11.11
Space-filling representation of the crystal structure of the
[3]catenane (
. Solvent molecules and
counter ions have been omitted for clarity. Color labeling
scheme: metallocycle, blue; inner cyclophanes, red; outer
cyclophanes, green.
DB24C8
)
M5a
·5NO
2
3
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