“…As for the tertiary amide-based polyacrylamides, it is more difficult to equip the polymers with thermoresponse than the secondary amide-based polyacrylamides due to the complexity to achieve hydrophobic-hydrophilic balance. As a result, one can easily prepare thermoresponsive polymers of the secondary amide polyacrylamides, [19][20][21][22][23][24][25][26][27][28][29][30][31][32][33][34][35][36][37] such as poly(N-methacryloyl-L -alanine methyl ester), 33 poly(N-acryloylglycine methyl ester) 34 , poly(N-acryloyl-Lproline methyl ester), 35 poly(N-acryloyl-L -phenylalanine methyl ester) 36 and poly(N-cyclopropylacrylamide), 37 In this work, we design and synthesize a thermoresponsive polymer, poly(N-acryloylsarcosine methyl ester) (PNASME, Scheme 1) with a tertiary amide group in the pendant. And the hydrophobic ester group was employed to counteract the hydrophilic tertiary amide group, making PNASME exhibiting a LCST-type phase transition behavior.…”