Abstract

ABSTRACTIn this work we study the possibility of the photochemical formation of the symmetrical Dewar pyridine (1-azabicyclo-[2,2,0]-hexa-2,5-diene), by applying the complete active space self-consistent field method and the multiconfigurational second-order perturbation theory to explore the corresponding ground and excited state potential energy surfaces. According to our theoretical calculations there are three possible paths that can be followed, one is a biphotonic process which involves irradiating pyridine in its ground state with a 358 nm laser guiding the system to an intersystem crossing S1/T1/S0 of triple character whereby deactivation to the ground state, S0, Dewar minimum occurs, the second one, which is a ground state thermal reaction involves the use of a far-Infra-Red laser where planar pyridine is vibrationally excited to a very high vibrational level whose energy is comparable to that of the ground state transition structure, S0(TS), connecting the symmetrical S0 Dewar pyridine and the ground state of planar pyridine. The third process is also a biphotonic one involving excitation of planar pyridine with an energy which is in the limits of its ionisation potential. In this case there is a theoretically accessible S1/S0 Conical Intersection which leads directly to the ground state of the symmetrical Dewar pyridine.

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