作者: T. Guérin , O. Bénichou , R. Voituriez
DOI: 10.1063/1.4792437
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摘要: We investigate theoretically the physics of diffusion-limited intramolecular polymer reactions. The present work completes and goes beyond a previous study [T. Guerin, O. Benichou, R. Voituriez, Nat. Chem. 4, 568 (2012)10.1038/nchem.1378] that showed distribution conformations at very instant reaction plays key role in cyclization kinetics, takes explicitly into account non-Markovian nature reactant motion. Here, we detail this theory, compare it with existing Markovian theories numerical stochastic simulations. A large focus is made on description non-equilibrium reactive conformations, both analytical tools. show are elongated characterized by spectrum slowly decreasing tail, implying monomers neighbor significantly shifted reaction. complete deri...