Description:
<jats:title>Abstract</jats:title><jats:p>Several years ago the photoinduced reaction of mixed phosphonium‐iodonium ylides (<jats:bold>1</jats:bold>) with acetylenes (<jats:bold>2</jats:bold>) to give λ<jats:sup>5</jats:sup>‐phosphinolines (<jats:bold>3</jats:bold>) and substituted furans (<jats:bold>4</jats:bold>) was described. This reaction is one‐pot, metal‐free synthesis of heterocycles <jats:bold>3</jats:bold> and <jats:bold>4</jats:bold> with the yields of 40% to 80%. The reaction proceeds only in dichloromethane (DCM) at the high ylide concentrations (>0.01 mol/L). The product analysis by <jats:sup>31</jats:sup>P NMR, electrospray ionization mass spectrometry, UV‐vis spectrophotometry, and the dynamic light scattering study of the self‐aggregation of the ylide in DCM showed a dual role of the solvent in the photoinduced reactions of mixed phosphonium‐iodonium ylide: (i) at the low ylide concentrations (<0.01 mol/L), the conjugated photoinitiation of the chain reaction in DCM results in the formation of chlorine‐containing products and (ii) at the high ylide concentrations (>0.01 mol/L), the photolysis mechanism is determined by self‐organization of the ylide molecules to give large stable aggregates in DCM, in which the target heterocycles are synthesized. Two important issues follow from the study. First, the annulation reaction between mixed phosphonium‐iodonium ylide and acetylenes occurs only when the reactive intermediates are in close proximity to one other, and, second, DCM is not inert reagent in reactions occurring with participation of radicals and in one form or another can participate in photoinduced radical reactions of various solutes.</jats:p>