The synthesis of two novel series of optically active methacrylic copolymers containing a side-chain chiral moiety linked to a photochromic bisazoaromatic chromophore has been carried out by radical copolymerization of monomer (S)-3-methacryloyloxy-1-[4’-phenylazo-(4-azobenzene)]-pyrrolidine with highly sterically hindering monomers such as tert-butyl methacrylate or triphenylmethyl methacrylate with the aim to investigate the effect on the optical activity of the resulting derivatives. The copolymeric products have been fully characterized and their spectroscopic and thermal properties compared to those of the related optically active homopolymer and the copolymers with methyl methacrylate, previously reported.The optical activity displayed by the polymers is discussed in terms of extent of chiral conformations assumed by the macromolecules as a consequence of the insertion of co-monomers capable to affect the dipole-dipole interactions occurring in these derivatives between the side-chain bisazoaromatic chromophores disposed according to a mutual chiral arrangement.
Optically active methacrylic copolymers bearing side-chain bisazoaromatic and bulky achiral moieties
MAURIELLO FRANCESCO;
2007-01-01
Abstract
The synthesis of two novel series of optically active methacrylic copolymers containing a side-chain chiral moiety linked to a photochromic bisazoaromatic chromophore has been carried out by radical copolymerization of monomer (S)-3-methacryloyloxy-1-[4’-phenylazo-(4-azobenzene)]-pyrrolidine with highly sterically hindering monomers such as tert-butyl methacrylate or triphenylmethyl methacrylate with the aim to investigate the effect on the optical activity of the resulting derivatives. The copolymeric products have been fully characterized and their spectroscopic and thermal properties compared to those of the related optically active homopolymer and the copolymers with methyl methacrylate, previously reported.The optical activity displayed by the polymers is discussed in terms of extent of chiral conformations assumed by the macromolecules as a consequence of the insertion of co-monomers capable to affect the dipole-dipole interactions occurring in these derivatives between the side-chain bisazoaromatic chromophores disposed according to a mutual chiral arrangement.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
