|Title||An investigation of the solid-state photochemistry of alpha-mesitylacetophenone derivatives: Asymmetric induction studies and crystal structure-reactivity relationships|
|Publication Type||Journal Article|
|Year of Publication||2000|
|Authors||Cheung, E, Rademacher, K, Scheffer, JR, Trotter, J|
|Type of Article||Article|
|Keywords||ABSTRACTION, ASYMMETRIC INDUCTION, CARBOXYLATE SALTS, CYCLIZATION, PHOTOCHEMISTRY, TRIPLETS, YANG PHOTOCYCLIZATION REACTION|
The photochemical conversion of a series of alpha-mesitylacetophenone derivatives into 2-indanols via delta-hydrogen abstraction has been investigated in the solid state. A correlation between solid-state reactivity and crystal structure has been established for this type of reaction. For the seven compounds whose crystal structures were determined, the average value of d (C=O...H distance) and L (C=O...CH3 distance) were 2.77+/-0.04 Angstrom and 3.42+/-0.06 Angstrom, and the value of omega (delta-H out of plane angle), d (C=O...H angle) and a (C-H...O angle) were 59+/-2 degrees, 80+/-7 degrees and 123+/-3 degrees, respectively. These parameters depended mainly on the magnitude of the deviation of the carbonyl group from the fully bisecting position over the mesityl ring, which ranged from 9-14 degrees in the case of in the solid state reactive ketones and approached 0 degrees for the unreactive compounds. Asymmetric induction studies were carried out by providing the reactants with carboxylic acid substituents to which ionic chiral auxiliaries were attached through salt formation with optically active amines. Irradiation of the salts (13 in total) in the crystalline state gave enantiomeric excesses of up to 90%. The crystal structures of three of the salts were determined and on this basis, the reasons for the selectivity in the crystalline state are discussed. (C) 2000 Elsevier Science Ltd. All rights reserved.
|URL||<Go to ISI>://000089149100018|