Surface grafting of poly(L-glutamates). 3. Block copolymerization

This paper describes for the first time the synthesis of surface-grafted AB -block copolypeptides, consisting of poly(gamma -benzyl L-glutamate) (PBLG) as the A-block and poly(gamma -methyl L-glutamate) (PMLG) as the B-block. Immobilized primary amine groups of (,gamma -aminopropyl)triethoxysilane (A PS) on silicon wafers initiated the ring-opening polymerization of N-carbox yanhydrides of glutamic acid esters (NCAs). After removal of the BLG-NCA mo nomer solution after a certain reaction time, the amine end groups of the f ormed PBLG blocks acted as initiators for the second monomers. This method provides the possibility of making layered structures of surface-grafted bl ock copolymers with tuned properties. Ellipsometry and small-angle X-ray re flection (SAXR) measurements revealed the thickness of the polypeptide laye rs ranging from 45-100 Angstrom of the first block to 140-270 Angstrom for the total block copolypeptides. The chemical composition of the blocks was determined by X-ray photoelectron spectroscopy (XPS). In addition, Fourier transform infrared transmission spectroscopy (FT-IR) revealed that the poly peptide main chains of both blocks consisted of pure a-helices. The average orientation of the helices ranging from 22-42 degrees with respect to the substrate within the first block to 31-35 degrees in the second block could be derived with FT-IR as well.