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SCANÂ AUTOCADÂ BIOMEDICALÂ KUNG FUÂ K&FÂ PDMLÂ PDMLÂ SOLIDWORKSÂ SURVESÂ TBSÂ WINGITÂ VLSÂ WINGITÂ ..Borodin and Antonenko [@CR5]; Lehtola et al. [@CR15]; Nielsen [@CR21]) and leading to the formation of additional de-excited complexes. This could be the underlying cause of the increase in the number of charges on the product side of the reaction. The increase in the number of charges could be a result of the higher content of 3-methyl-4-nitrosopyridine in the *E*-isomer of IvaRot versus the *Z*-isomer of IvaRot-1-MeOH, respectively. This might also explain the increased peak intensity of the nitrosamine, in the de-excited states. In addition, bimolecular radiative N atom loss, in which two reaction partners share the energy, could be responsible for the increased radiative lifetime and the higher number of charges. Finally, the formation of additional de-excited complexes could result in non-radiative quenching. Thus, the increase in the number of charges in the products could be a result of the formation of additional de-excited complexes in addition to the already formed de-excited complexes. Photochemistry of IvaRot {#Sec11} ———————— The photochemistry of IvaRot was investigated in this study. Using the steady-state photocatalysis and autocatalysis, IvaRot was shown to produce N~2~ (product **P1**) in the presence of spin traps (Fig. [4](#Fig4){ref-type=»fig»}).Fig. 4Time-dependent consumption of **P1**, the only product observed, during irradiation of IvaRot (a) without added spin traps; (b) with added DMPO; and (c) with added 2-POBN. The fraction of IvaRot in the reaction mixture was 10 mM In the ^1^O~2~-mediated photochemical reaction, the N~2~ (product **P1**) is only formed when O~2~ has been consumed in c6a93da74d
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