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(a)
HO 2 C
CH 2
CH
Heating
O
n
NHS, DCC
NH
NH 2
Cooling
H 3 C
CH 3
PNIPAAm
(b)
CN
CN
(CH 2 ) 2
C
N
N
C
(CH 2 ) 2
CO 2 H
CH 3
CH 3
Heating
O
(CH 2 ) 3
N
H
O
Si
O
CH=CH 2
Cross-linking
agent
Cooling
CH 3
O
O
H
CH
CH 3
NIPAAm
Initiator-immobilized surface
(c)
CH=CH 2
CH 3
O
H
CH
Heating
O
CH 2 Cl
CH 3
NIPAAm
O
Si
(CH 2 ) 2
Cooling
CuCl, Me 6 TREN
O
Above LCST
Below LCST
ATRP Initiator-immobilized surface
Expanded
PNIPAAm
Shrunken
PNIPAAm
Figure 20.2 Preparation of a PNIPAAm modified high-functionality surface using (a) terminal modification method, (b) gel modification
method and (c) ATRP method. NHS; N-Hydroxysuccinimide, DCC; Dicyclohexylcarbodiimide, Me 6 TREN; Tris(2-(dimethylamino)ethyl)amine.
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