Issue 10, 2011

Poly(N-protected ethylene imine-alt-ethylene sulfide) block to functionalize polymeric materials

Abstract

Poly(N-tosyl-ethylene imine-alt-ethylene sulfide) has been synthesized by thiol-ene photopolymerization between N,N-bis(2-mercaptoethyl)-4-methylbenzenesulfonamide and 4-methyl-N,N-divinylbenzenesulfonamide. Its weight-average molecular weight was determined by static light scattering to be 2.8 × 104. The alternating copolymer has –SH and –CH=CH2 end groups and exhibits high solubility in common organic solvents such as chloroform, tetrahydrofuran, acetone, and dimethyl sulfoxide. The N-tosylated copolymer was deprotected to yield poly(ethylene imine-alt-ethylene sulfide), which is fully soluble in dimethyl sulfoxide, acetic acid, and ethanol. Both N-tosylated and deprotected polymers are hydrophobic, and the former and latter polymers are thermally decomposed at 272 and 244 °C, respectively.

Graphical abstract: Poly(N-protected ethylene imine-alt-ethylene sulfide) block to functionalize polymeric materials

Supplementary files

Article information

Article type
Communication
Submitted
10 Jun 2011
Accepted
13 Jul 2011
First published
11 Aug 2011

Polym. Chem., 2011,2, 2183-2185

Poly(N-protected ethylene imine-alt-ethylene sulfide) block to functionalize polymeric materials

Y. Hori, N. Pei, R. Kumagai and Y. Sasanuma, Polym. Chem., 2011, 2, 2183 DOI: 10.1039/C1PY00264C

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