Add time:08/05/2019         Source:sciencedirect.com

The reaction mechanism in the UV photochemistry of 2-chloro-2′-deoxyadenosine (Cladibrine) and 2-bromo-2′-deoxyadenosine in aqueous solution has been studied by laser photolysis at nanosecond time resolution. It is found that excitation at 266 nm wavelength produces heterolytic cleavage of the halogen-carbon bond by one-photon absorption and formation of the unstable 2-hydroxy tautomer of 2′-deoxyisoguanosine as predominant ‘primary’ product. The 2-hydroxy tautomer then transforms in 10−6-10−5 s into the stable 2-oxo tautomer in an acid-base-catalysed reaction. A reaction mechanism is proposed and discussed in relation to previous UV low-intensity studies of these halogenodeoxyadenosines.

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