Anion-molecule nucleophilic substitution (S(N)2) reactions are known for their rich reaction dynamics, caused by a complex potential energy surface with a submerged barrier and by weak coupling of the relevant rotational-vibrational quantum states. The dynamics of the S(N)2 reaction of Cl- + CH3I were uncovered in detail by using crossed molecular beam imaging. As a function of the collision energy, the transition from a complex-mediated reaction mechanism to direct backward scattering of the I- product was observed experimentally. Chemical dynamics calculations were performed that explain the observed energy transfer and reveal an indirect roundabout reaction mechanism involving CH3 rotation.
The highly exoergic nucleophilic substitution reaction F(-) + CH3I shows reaction dynamics strikingly different from that of substitution reactions of larger halogen anions. Over a wide range of collision energies, a large fraction of indirect scattering via a long-lived hydrogen-bonded complex is found both in crossed-beam imaging experiments and in direct chemical dynamics simulations. Our measured differential scattering cross sections show large-angle scattering and low product velocities for all collision energies, resulting from efficient transfer of the collision energy to internal energy of the CH3F reaction product. Both findings are in strong contrast to the previously studied substitution reaction of Cl(-) + CH3I [Science 2008, 319, 183-186] at all but the lowest collision energies, a discrepancy that was not captured in a subsequent study at only a low collision energy [J. Phys. Chem. Lett. 2010, 1, 2747-2752]. Our direct chemical dynamics simulations at the DFT/B97-1 level of theory show that the reaction is dominated by three atomic-level mechanisms, an indirect reaction proceeding via an F(-)-HCH2I hydrogen-bonded complex, a direct rebound, and a direct stripping reaction. The indirect mechanism is found to contribute about one-half of the overall substitution reaction rate at both low and high collision energies. This large fraction of indirect scattering at high collision energy is particularly surprising, because the barrier for the F(-)-HCH2I complex to form products is only 0.10 eV. Overall, experiment and simulation agree very favorably in both the scattering angle and the product internal energy distributions.
Studies of charge transfer are often hampered by difficulties in determining the charge localization at a given time. Here, we used ultrashort x-ray free-electron laser pulses to image charge rearrangement dynamics within gas-phase iodomethane molecules during dissociation induced by a synchronized near-infrared (NIR) laser pulse. Inner-shell photoionization creates positive charge, which is initially localized on the iodine atom. We map the electron transfer between the methyl and iodine fragments as a function of their interatomic separation set by the NIR-x-ray delay. We observe signatures of electron transfer for distances up to 20 angstroms and show that a realistic estimate of its effective spatial range can be obtained from a classical over-the-barrier model. The presented technique is applicable for spatiotemporal imaging of charge transfer dynamics in a wide range of molecular systems.
The understanding of molecular structure and function is at the very heart of
the chemical and molecular sciences. Experiments that allow for the creation of
structurally pure samples and the investigation of their molecular dynamics and
chemical function have developed tremendously over the last few decades,
although "there's plenty of room at the bottom" for better control as well as
further applications.
Here, we describe the use of inhomogeneous electric fields for the
manipulation of neutral molecules in the gas-phase, \ie, for the separation of
complex molecules according to size, structural isomer, and quantum state. For
these complex molecules, all quantum states are strong-field seeking, requiring
dynamic fields for their confinement. Current applications of these controlled
samples are summarised and interesting future applications discussed.Comment: Accepted by Int. Rev. Phys. Che
Solvents have a profound influence on chemical reactions in solution and have long been used to control their outcome. Such effects are generally considered to be governed by thermodynamics; however, little is known about the steric effects of solvent molecules. Here, we probe the influence of individual solvent molecules on reaction dynamics and present results on the atomistic dynamics of a microsolvated chemical reaction--the fundamentally important nucleophilic substitution reaction. We study the reaction of OH(-) with CH(3)I using a technique that combines crossed-beam imaging with a cold source of microsolvated reactants. Our results reveal several distinct reaction mechanisms for different degrees of solvation; surprisingly, the classical co-linear substitution mechanism only dominates the dynamics for mono-solvated reactants. We analyse the relative importance of the different mechanisms using ab initio calculations and show that the steric characteristics are at least as relevant as the energetics in understanding the influence of solvent molecules in such microsolvated reactions.
Ion imaging experiments and direct chemical dynamics simulations were performed to study the atomic-level dynamics for the Fþ CH 3 I f FCH 3 þ I -S N 2 nucleophilic substitution reaction at 0.32 eV collision energy. The simulations reproduce the product energy partitionings and the velocity scattering angle distribution measured in the experiments. The simulations reveal that the substitution reaction occurs by two direct atomic-level mechanisms, that is, rebound and stripping, and an indirect mechanism. Approximately 90% of the indirect events occur via a prereaction F -3 3 3 HCH 2 I hydrogen-bonded complex. This mechanism may play an important role for other F -S N 2 reactions due to the strong electronegativity of fluorine. The average product energy partitioning for the Fþ CH 3 I indirect mechanism agrees with the prediction of PST, even though a FCH 3 3 3 3 Ipostreaction complex is not formed.
Ionization and fragmentation of methylselenol (CH 3 SeH) molecules by intense (> 10 17 W=cm 2 ) 5 fs x-ray pulses (@! ¼ 2 keV) are studied by coincident ion momentum spectroscopy. We contrast the measured charge state distribution with data on atomic Kr, determine kinetic energies of resulting ionic fragments, and compare them to the outcome of a Coulomb explosion model. We find signatures of ultrafast charge redistribution from the inner-shell ionized Se atom to its molecular partners, and observe significant displacement of the atomic constituents in the course of multiple ionization.
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