Gabbutt, Christopher D., Heron, B. Mark, Mars, Craig A. and Partington, Steven M. (2005) Synthesis and Photochromic Properties of 2H,9H-Indeno[1,2-f]- and 3H,7H-Indeno[2,1-i]- naphtho[2,1-b]pyrans. Molecular Crystals and Liquid Crystals, 430 (1). pp. 167-172. ISSN 1542-1406Metadata only available from this repository.
Expedient syntheses of the 3-hydroxy- and 6-hydroxy- derivatives of 11H-benzo[a]fluoren-11-one, obtained via Suzuki-Miyaura couplings are described. Reactions of these phenols with 1,1-diarylprop-2-yn-1-ols give indeno[2,1-i]- and indeno[1,2-f]- naphtho[2,1-b]pyranones respectively. The photochromic properties of these and the reduced derivatives are reported. A rationale for the pronounced hypsochromic shift in λmax of the photomerocyanine from a 2H,9H-indeno[1,2-f]naphtho[2,1-b]pyran is presented.
|Subjects:||Q Science > Q Science (General)|
Q Science > QD Chemistry
|Schools:||School of Applied Sciences|
|Depositing User:||Sharon Beastall|
|Date Deposited:||25 Sep 2012 13:35|
|Last Modified:||18 Oct 2012 09:45|
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