## Abstract **New route to gas‐phase OH^.^**: UV photolysis of gaseous __o__‐nitrobenzaldehyde forms OH radicals via the transformation into the ketene or __o‐__nitrosobenzoic acid intermediate (see figure). The OH^.^ product is monitored by single‐photon laser‐induced fluorescence (LIF).magnified
Photolysis of dimethylnitrosamine in the gas phase
✍ Scribed by Georg Geiger; J. Robert Huber
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- German
- Weight
- 394 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Photodecomposition of dimethylnitrosamine in the gas phase (-1 Torr) has been investigated following irradiation into the S, ( n n * ) t S , (363.5 nm) and S, ( m * ) t S , (248.1 nm) transitions at room temperature. With a quantum yield of unity, excitation into the S, state yields the fragments (CH,),N' and NO which then recombine leaving no photoproducts. The addition of 0, results in only one photoproduct, (CH,),NNO,.
Irradiating into the S, state, the products CH,=N-CH,, (CH,=N-CH,),, CH,=NOH, N20, NO, H,, and N, were identified by capillary gas chromatography mass spectrometry. In the presence of N, as a buffer gas the photoproducts are only CH,=N-CH,, (CH,=N-CH,),, N,O, and H,. For both excitation conditions a mechanism is proposed involving cleavage of the N, N-bond as the main primary photolytic process.
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A(AGI: 4 f l kcal.mol.' Scheme 1. Stability sequence ofcations (1) to (6); D(R@ X"') values taken from l3bl.