Spacer-Length-Dependent Association in Polymers with Multiple-Hydrogen-Bonded End Groups

De Greef, Tom F. A.; Kade, Matthew J.; Feldman, Kathleen E.; Kramer, Edward J.; Hawker, Craig J.; Meijer, E. W.
J. Polym. Sci., Polym. Chem.,
2011
49, 4253-4260.

Herein, we investigate the influence of spacer length on the homoassociation and heteroassociation of end-functionalized hydrogen-bonding polymers based on poly(n-butyl acrylate). Two monofunctional ureido-pyrimidinone (UPy) end-functionalized polymers were prepared by atom transfer radical polymerization using self-complementary UPy-functional initiators that differ in the spacer length between the multiple-hydrogen-bonding group and the chain initiation site. The self-complementary binding strength (Kdim) of these end-functionalized polymers was shown to depend critically on the spacer length as evident from 1H NMR and diffusion-ordered spectroscopy. In addition, the heteroassociation strength of the end-functionalized UPy polymers with end-functionalized polymers containing the complementary 2,7-diamido-1,8-naphthyridine (NaPy) hydrogen-bond motif is also affected when the aliphatic spacer length is too short.