Theoretical verification of nonthermal microwave effects on intramolecular reactions.

There have been a growing number of articles that report dramatic improvements in the experimental performance of chemical reactions by microwave irradiation compared to that under conventional heating conditions. We theoretically examined whether nonthermal microwave effects on intramolecular reactions exist or not, in particular, on Newman-Kwart rearrangements and intramolecular Diels-Alder reactions. The reaction rates of the former calculated by the transition state theory, which consider only the thermal effects of microwaves, agree quantitatively with experimental data, and thus, the increases in reaction rates can be ascribed to dielectric heating of the solvent by microwaves.

Experimental and theoretical investigations of isomerization reactions of ionized acetone and its dimer.

Ionization dynamics of acetone and its dimer in supersonic jets is investigated by a combination of experimental and theoretical techniques, both of which have recently been developed. In experiments, the neutral and the cationic structures are explored by infrared predissociation spectroscopy with the vacuum-ultraviolet photoionization detection schemes. Reaction paths following the one-photon ionization of the acetone monomer and its dimer have been studied by the joint use of several theoretical methods including the ab initio molecular dynamics, the global reaction route mapping, the intrinsic reaction coordinate, and the artificial force induced reaction calculations.

Quantum dynamics of light-driven chiral molecular motors.

The results of theoretical studies on quantum dynamics of light-driven molecular motors with internal rotation are presented. Characteristic features of chiral motors driven by a non-helical, linearly polarized electric field of light are explained on the basis of symmetry argument. The rotational potential of the chiral motor is characterized by a ratchet form.

Quantum optimal control of electron ring currents in chiral aromatic molecules.

We report the results of optimal control simulations of pi-electron rotation (ring current) in a six-membered chiral aromatic molecule, 2,5-dichloro[n](3,6)pyrazinophane (DCP), attached at a surface and excited by a linearly polarized UV laser. DCP has a pair of optically allowed, quasidegenerate pi-electronic excited states. The laser pulse to generate an approximate angular momentum eigenstate consisting of the quasidegenerate states was designed using the global optimal control theory.

Theoretical design of an aromatic hydrocarbon rotor driven by a circularly polarized electric field.

An aromatic hydrocarbon rotor without functional groups is theoretically designed. Such a molecular rotor is free from long-range electrostatic interactions. Induced dipole interactions are the rotor-driving forces under a nonresonant excitation condition.

Mechanisms in adaptive feedback control: photoisomerization in a liquid.

The underlying mechanism for Adaptive Feedback Control in the experimental photoisomerization of 3,3'-diethyl-2,2'-thiacyanine iodide (NK88) in methanol is exposed theoretically. With given laboratory limitations on laser output, the complicated electric fields are shown to achieve their targets in qualitatively simple ways. Further, control over the cis population without laser limitations reveals an incoherent pump-dump scenario as the optimal isomerization strategy.

Quantum control of a chiral molecular motor driven by laser pulses.

"Molecular motors or machines" are one of the hot subjects in chemistry because they play an important role in molecular devices. We have theoretically demonstrated that unidirectional rotations of a chiral molecular motor can be driven by using tailored linearly polarized laser pulses. The findings obtained here serve as a theoretical basis for control of functions such as gearing or acceleration of molecular motors.