Quantum yield photonitrosation

The crucial requirement of excited-state proton transfer (ESPT) is suggested by the failure of 1-naphthyl methyl ether to undergo self-nitrosation under similar photolysis conditions. The ESPT is further established by quenching of the photonitrosation as well as 1-naphthol fluorescence by general bases, such as water and triethylamine, with comparable quenching rate constants and quantum yield. ESPT shows the significance in relation to the requirement of acid in photolysis of nitrosamines and acid association is a photolabile species. 

Aliphatic and alicyclic molecules such as cyclohexane undergo photosubstitution with nitrosyl chloride (Pape, l%7). The reaction is of considerable industrial importance in the synthesis of 6-caprolactam, an intermediate in the manufacture of polyamides (nylon 6). (Cf. Fischer, 1978.) At long wavelengths a cage four-center transition state between alkane and an excited nitrosyl chloride molecule is involved, as indicated in Scheme 63. In contrast to light-induced halogenation, photonitrosation has a quantum yield smaller than unity, and is not a chain reaction. 

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See also in sourсe #XX -- [ ]

See also in sourсe #XX -- [ ]

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