Optically active methacrylic copolymers with side-chain azoaromatic and 9-phenylcarbazole moieties

2012 ◽  
Vol 72 (1) ◽  
pp. 1-10 ◽  
Author(s):  
Luigi Angiolini ◽  
Loris Giorgini ◽  
Francesco Mauriello ◽  
Paul Rochon
Keyword(s):  
2007 ◽  
Vol 208 (14) ◽  
pp. 1548-1559 ◽  
Author(s):  
Luigi Angiolini ◽  
Tiziana Benelli ◽  
Loris Giorgini ◽  
Francesco Mauriello ◽  
Elisabetta Salatelli
Keyword(s):  

1994 ◽  
Vol 27 (14) ◽  
pp. 3721-3726 ◽  
Author(s):  
L.-C. Chien ◽  
Leonorina G. Cada

1985 ◽  
Vol 18 (4) ◽  
pp. 729-734 ◽  
Author(s):  
Angelina Altomare ◽  
Carlo Carlini ◽  
Francesco Ciardelli ◽  
Mario Panattoni ◽  
Roberto Solaro ◽  
...  

e-Polymers ◽  
2003 ◽  
Vol 3 (1) ◽  
Author(s):  
Luigi Angiolini ◽  
Loris Giorgini ◽  
Elisabetta Salatelli

Abstract The optically active photochromic homopolymer deriving from radical polymerization of the monomer (R)-3-methacryloyloxy-1-(4’-nitro-4-azobenzene)- pyrrolidine, containing a chiral group of one prevailing configuration interposed between the methacrylic moiety and the photochromic azoaromatic chromophore, has been synthesized and characterized. Copolymers with the enantiomeric monomer (S)-3-methacryloyloxy-1-(4’-nitro-4-azobenzene)pyrrolidine have also been prepared in order to evaluate the effect on the overall optical activity of side chain chiral groups of opposite configuration in various ratios. The spectroscopic and chiroptical properties in solution of the polymeric derivatives have been assessed.


2012 ◽  
Vol 72 (7) ◽  
pp. 469-477 ◽  
Author(s):  
Luigi Angiolini ◽  
Tiziana Benelli ◽  
Erika Bicciocchi ◽  
Loris Giorgini ◽  
Françisco M. Raymo
Keyword(s):  

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