Photochemische Reaktionen 49. Mitteilung [1] Spezifisch π → π*-induzierte Keton-Photoreaktionen: Die Doppelbindungsverschiebung von O-Acetyl-10α-testosteron Protonisierung der Doppelbindung seines δ5-Isomeren

The α,β-unsatured ketone 10α-testosterone has been reported previously 6] to photoisomerize in t-butanol solution to the β,γ-unsaturated ketone. The irradiation had been carried out using a high-pressure mercury lamp in a quartz vessel. For structural reasons this double bond shift cannot proceed through a photoenolization mechanism involving an intramolecular hydrogen transfer from the γ-position to the enone oxygen as has been suggested to operate in several formally analogous cases of aliphatic enone isomerizations. In the present reinvestigation, O-acetyl 10α-testosterone ( 1 ) was used, employing selectively either excitation of its n → π* (with wavelengths > 300 nm) or its π → π* absorption band (with 253,7 nm). In t-butanol solution the doublebond shift 1 → 2 could be effected with π→* excitation only. Experiments in deuterated solvent (t-BuOD) resulted in deuterium in corporation in both the δ5-ketone in the C(4)-position, cf.( 3 ) and in the conjugated ketone. These results indicate that the reactions is initiated either in the, S_π,π* state or in a high vibrational mode of the S₀ or t_ππ*state. n→ π* Excitation of 1 in t-butanol gave essentially no over-all chemical change, while in benzene solution it resulted again in a double bond isomerization ( 1 → 2 ). In analogy to results with similar enones 28] under identical conditions the deconjugation in benzene may be the consequence of an intermolecular hydrogen abstraction of the T_n,π* excited state of the enone. Another specifically π →π* induced photoreaction was observed on irradiation of the β, γ-unsaturated ketone 2 in t-BuOD with 253,7 nm. The olefinic hydrogen at C-6 of 2 was exchanged with deuterium and, to a small extent, isomerization to the conjugated ketone 1 with concomitant deuterium incorporation occurred. It is concluded that from the higher excited state of the β, γ-unsaturated ketone, but not from its S_n,π* state, an activation mode of the double bond is accessible to effect D+ addition at C-6 followed by deprotonation to 4 and to deuterated 1 , respectively.