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Many organic molecules are photolabile in nature and can be used to investigate and explain the photochemistry of biomolecules. However, as with many synthetic organic molecules the photochemistry of these compounds is complicated by the presence of reactive groups that may be sterically hindering. This is due to the need to increase the efficiency of an otherwise inefficient photochemical reaction. For instance, it is important to have a singlet state triplet state efficient energy transfer.
It is known that aromatic amines may be photodeprived of energy by either irreversible hydrogen abstraction or by energy transfer, i.e. photobringing. Irreversible hydrogen abstraction has been used to photobride many types of aromatic amines. Typically, the radical formed by abstraction has a very high excited state potential energy, E. The amine photobrides with the excited state radical in a transition state, E.sub.ts -E. The hydrogen abstraction is less efficient than energy transfer but is more specific for the type of radical formed and thus can be used to selectively photobride. The photobriding can also be reversed upon irradiation with visible light, for instance, by irradiation with visible light.
Energy transfer, i.e. photobringing, can be used to photobride aromatic amines, for example, at 77 K. The aromatic amine-radical system can be photoexcited at a wavelength where the aromatic amine is in an n.pi. or pi.pi.*. state, for instance, at 5.mu.m, and the energy can be transferred to the radical upon formation of a low
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