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9-Anthracenyl-substitued pyridyl enones revisited : photoisomerism in ligands and silver(I) complexes
Journal
Dalton Transactions
Volume
40
Number
45
Pages / Article-Number
12146-12152
Abstract
In solution, (E) to (Z)-isomerism is facile both in 3-(9-anthracenyl)-1-(pyridin-4-yl) propenone, 2, and in its silver(I) complex [Ag(2)(2)](+). The crystal structures of (E)-2, (Z)-2 and [Ag(E)-2(2)][SbF6] are presented, and the roles of edge-to-face and face-to-face p-interactions in the lattice are discussed. Solution NMR spectroscopic data suggest that the driving force for (E) to (Z) isomerization is intramolecular p-stacking of the pyridine and anthracene domains. The reversed enone 3-(9-anthracenyl)-1-(pyridin-4-yl) propen-3-one, (E)-3, and the silver(I) complex [Ag(E)-3(2)][SbF6] have been prepared and characterized, including a single crystal X-ray determination of the latter. Surprisingly, no p-stacking between anthracene or pyridine domains is observed in the solid state, and the crystal packing is dominated by Ag center dot center dot center dot F, CHanthracene center dot center dot center dot pi-pyridine and CH center dot center dot center dot F interactions. In contrast to (E)-2 and [Ag(E)-2(2)](+), neither (E)-3 nor [Ag(E)-3(2)](+) undergoes photoisomerization in solution.
