Abstract
A range of aryl ether linked benzophenones (8) has been conveniently obtained by nucleophilic displacement of fluoride from 4-fluorobenzophenone with a dihydroxy-benzene or -naphthalene. The linked benzophenones were efficiently transformed in two steps to symmetrically linked naphthopyrans (10d-k). The photochromic response of these novel systems under steady state irradiation is characterised by a two stage fading process and their colourability is only marginally improved over the related monomeric analogues (10a-c).
Original language | English |
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Pages (from-to) | 24-34 |
Number of pages | 11 |
Journal | Dyes and Pigments |
Volume | 76 |
Issue number | 1 |
Early online date | 5 Jan 2006 |
DOIs | |
Publication status | Published - 1 Jan 2008 |
Externally published | Yes |