Abstract
Hyperbranched polyethylenimine terminated with isobutyramide groups (HPEI-IBAm) was mixed with 4-(phenylazo)benzoic acid (PABA) to form supramolecular complexes through the neutralization reaction between the amino groups of HPEI-IBAm and the carboxylic acid group of PABA, which was verified by 1H and 2D NOESY 1H NMR spectroscopy. The obtained supramolecular complexes with a molar ratio of PABA to HPEI-IBAm of ≤8 were soluble in water and exhibited thermoresponsive properties. Their cloud point temperature (Tcp) was sensitive to PABA content, and PABA molecules were exchanged between HPEI-IBAm hosts. The topology of the polymer affected the change in Tcp of the complexes. At pH ∼7, increasing the PABA content decreased Tcp, whereas it caused Tcp to increase at pH ∼9. Reversible trans-to-cis photoisomerization of azobenzene units in the complexes occurred following irradiation with UV or visible light. At pH ∼7, trans-to-cis isomerization of azobenzene units increased Tcp, whereas the opposite occurred at pH ∼9.
| Original language | English |
|---|---|
| Pages (from-to) | 67-71 |
| Number of pages | 5 |
| Journal | ACS Macro Letters |
| Volume | 2 |
| Issue number | 1 |
| DOIs | |
| State | Published - 15 Jan 2013 |