The synthesis by radical homopolymerization of a novel optically active methacrylic polymer containing a side-chain chiral moiety linked to a photochromic chromophore has been carried out starting from the related monomer trans-(S)-(+)-N-methyl-(2-methacryloyloxypropanoyl)-4-aminoazobenzene. The chiroptical properties in solution of the polymer have been investigated by circular dichroism and compared with those of the corresponding low molecular weight model compound, trans-(S)-(+)-N-methyl-(2-pivaloyloxypropanoyl)-4-aminoazobenzene. The optical activity displayed by the polymer is discussed in terms of extent of chiral conformations assumed by the macromolecules as a consequence of dipole-dipole interactions between the azoaromatic chromophores.

METHACRYLIC POLYMERS BEARING IN THE SIDE-CHAIN AN OPTICALLY ACTIVE MOIETY LINKED TO THE TRANS-4-AZOBENZENE CHROMOPHORE: CHIROPTICAL PROPERTIES OF POLY[(S)-(+)-N-METHYL-(2-METHACRYLOYLOXYPROPANOYL)-4-AMINOAZOBENZENE]

ANGIOLINI, LUIGI;GIORGINI, LORIS;SALATELLI, ELISABETTA
2004

Abstract

The synthesis by radical homopolymerization of a novel optically active methacrylic polymer containing a side-chain chiral moiety linked to a photochromic chromophore has been carried out starting from the related monomer trans-(S)-(+)-N-methyl-(2-methacryloyloxypropanoyl)-4-aminoazobenzene. The chiroptical properties in solution of the polymer have been investigated by circular dichroism and compared with those of the corresponding low molecular weight model compound, trans-(S)-(+)-N-methyl-(2-pivaloyloxypropanoyl)-4-aminoazobenzene. The optical activity displayed by the polymer is discussed in terms of extent of chiral conformations assumed by the macromolecules as a consequence of dipole-dipole interactions between the azoaromatic chromophores.
2004
L. Angiolini; L. Giorgini; E. Salatelli
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/7382
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