Abstract
AbstractThe substituted monomers 4a,c,d, 5a,b, 6a, 7a,b, and 8a of novel poly(diphenylamines), possessing the respective photochromic groups, were synthesized by the Stille cross‐coupling methodology (Scheme). The hyperbranched structures were characterized by 1H‐ and 13C‐NMR spectroscopy. The obtained monomers show good stability in common organic solvents such as CHCl3, toluene, and CH2Cl2, and exhibit excellent thermal stability. Electrochemical results and theoretical calculations suggest that oxidation and reduction of the monomers start from the side of the amine function and the five‐membered heterocyclic ring moieties, respectively.
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