Person:

Tang, Yiqiao

Fluorescent imaging of single helicene molecules is applied to study the optical activity of chiral fluorophores. In contrast to the previous report by Hassey et al. (Science 2006, 314, 1437), the dissymmetry factors of single chiral fluorophores are found not to differ significantly from the bulk value of |g| < 10^{−4} at 457 nm. Linear dichroism and birefringence of the dichroic mirror inside the fluorescence microscope change the polarization state of the incoming laser beam significantly; i.e., circular polarized light sent into the microscope becomes highly elliptically polarized after reflection from the dichroic mirror. Compensation for this effect should be made to avoid artifacts brought by linear dichroism in single immobilized molecules.

Metallic and magnetic nanostructures set electromagnetic boundary conditions which can lead to highly contorted fields in their immediate vicinity. While much attention has been devoted to enhancements in electric field strength, we argue that equally interesting phenomena arise from enhancements in magnetic and electric field gradients. Nonuniform fields near nanostructures can induce molecular transitions that are forbidden by electric dipole selection rules. We illustrate this claim with two examples. ‘‘Superhelical’’ electromagnetic fields are predicted to show enhanced asymmetry in their interaction with chiral molecules, far greater than that due to circularly polarized light. Such fields could be used to induce chiral photochemistry with large enantiomeric excess. Steeply varying DC magnetic fields are predicted to enhance the rate of intersystem crossing in molecular bi-radicals. Such fields could provide a route to new nanomagnetic catalysts and to magnetic control of chemical reactions.