Biomedical Engineering Reference
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R 2 R 3
R 1
R 1
R 2
X -
R 1
Br
N
R 1
R 2
R 3
O
R 2
14R 3
THF
B O
N
N
Br
N
R 3
Pd(PPh 3 ) 4
K 2 CO 3
THF/H 2 O
Br
X -
16
X -
N
Br
13
15
17a-e
R 3
R 1
R 2
R 3
R 2
N
X -
R 1
N
R 1
R 1
R 1
R 2
N
N
THF/CH 3 CN
n-BuLi
THF
R 2
N
R 2
Br
N
N
Br
R 3
N
Br
R 3
X -
R 3
X -
N
16
N
Br
14
18
19a-c
R 3
R 1
R 2
R 3
R 2
R 1
R 1
R 2
R 3
X -
O
O
R 1
N
R 1
R 2
R 3
THF/CH 3 CN
R 2
R 3
13
Br
N
N
Br
Pd(PPh 3 ) 4
K 2 CO 3
THF/H 2 O
N
Br
X -
X -
N
16
Br
20
21
22a-c
R 3
R 1
R 2
Figure 9.10 Synthesis routes to Benzene-based ionic liquid crystals.
71] have reported tripodal ionic liquid crystals based on pyridine ( 17a-e ),
pyrimidine ( 19a-c ) and quinoline ( 22a-c ) salts with benzene core at the
center. h ese salts were prepared by quarterization reactions of the cor-
responding phenylpyridine, phenylpyrimidine or phenylquinoline deriva-
tives with 1,3,5-tribromomethylbenzene followed by counterion exchange,
as shown in Figure 9.10. As we go from pyridine to quinoline salts, meso-
phase also changed from columnar rectangular to columnar hexago-
nal mesophase (Table 9.2). Also, as the size of the counterion decreased
from PF 6 to Br, additional cubic mesophases were observed, and when
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