Photochemical electrocyclic ring closure and leaving group expulsion from N-(9-oxothioxanthenyl)benzothiophene carboxamidesElectronic supplementary information (ESI) available: 1H-NMR COSY for 26, and 27. 1H-NMR NOESY for 27. X-diffraction data for 30. Comparison 1H-NMR between 27 and 30. 1H-NMR for a mixture of 30 and 31. 1H-NMR and 13C NMR spectra of all synthesized compound. Stern-Volmer quenching 8 (LG− = Cl−) by piperylene. Computed structures in Fig. 3 and 4. CCDC XXXXXX. For ESI and cryst

N -(9-Oxothioxanthenyl)benzothiophene carboxamides bearing leaving groups (LG − = Cl − , PhS − , HS − , PhCH 2 S − ) at the C-3 position of the benzothiophene ring system photochemically cyclize with nearly quantitative release of the leaving group, LG − . The LG − photoexpulsions can be conducted with 390 nm light or with a sunlamp. Solubility in 75% aqueous CH 3 CN is achieved by introducing a carboxylate group at the C-6 position of the benzothiophene ring. The carboxylate and methyl ester derivatives regiospecifically cyclize at the more hindered C-1 position of the thioxanthone ring. Otherwise, the photocyclization favors the C-3 position of the thioxanthone. Quantum yields for reaction are 0.01-0.04, depending on LG − basicity. Electronic structure calculations for the triplet excited state show that excitation transfer occurs from the thioxanthone to the benzothiophene ring. Subsequent cyclization in the triplet excited state is energetically favourable and initially generates the triplet excited state of the zwitterionic species. Expulsion of LG − is thought to occur once this species converts to the closed shell ground state. Water-soluble benzothiophenecarboxamides with thioxanthone attached to the amide nitrogen undergo 385 nm photolytic elimination of Cl − , PhS − , HS − , or PhCH 2 S − from the C-3 position of the benzothiophene ring system.