## Abstract The synthesis of a novel optically active methacrylic monomer containing in the side chain the (__S__)‐3‐hydroxy‐__N__‐phenyl pyrrolidine ring linked to a 4‐cyanophenylazocarbazole moiety [(__S__)‐**MCAPP**‐**C**] and of the analogous achiral monomer (**MCAPE‐C**) is described. Both the
Photochromic and Photoresponsive Properties of Methacrylic Polymers Bearing Optically Active Hydroxysuccinimide in the Side Chain
✍ Scribed by Luigi Angiolini; Tiziana Benelli; Loris Giorgini
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 253 KB
- Volume
- 208
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
The photochromic and photoresponsive properties of a series of optically active azoaromatic polymers, containing in the side chain the rigid (S)‐ and/or (R)‐hydroxysuccinimide residue, have been investigated in solution and in the solid state as thin films by observing the trans‐cis photoisomerisation of the azobenzene chromophore, and the results are compared to the corresponding monomeric (S) and (R) model compounds. The presence of exciton splitting due to dipole‐dipole interactions between the trans‐azoaromatic rings in the CD spectra confirms the intrinsic chirality of the macromolecules. Thin films of the polymers display the same chiroptical properties as the solution, thus suggesting that the macromolecules maintain chiral conformations also in the solid amorphous state.
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Experimental part ## Chemicals, monomers and models Methacryloyl chloride (Aldrich) was distilled (b. p. 95 8C) under inert atmosphere in the presence of traces of 2,6-ditert-butyl-p-cresol as polymerization inhibitor just before
Novel optically active polymethacrylates, namely poly[(S)-3-methacryloyloxy-1-(4-azobenzene)pyrrolidine] and poly[(S)-3-methacryloyloxy-1-(4Ј-nitro-4-azobenzene)pyrrolidine], have been synthesized by radical polymerization of the corresponding monomers, prepared in turn through a synthetic route pre
## Abstract Novel optically active monomers such as __trans__‐(__S__)‐4‐(2‐methacryloylaminopropano‐ylamino)azobenzene, __trans__‐(__S__)‐4‐(2‐methacryloyloxypropanoylamino)azobenzene, and __trans__‐(__S__)‐4‐(2‐acryloylaminopropanoylamino)azobenzene have been prepared and homopolymerized by free r