Abstract
Fluorescence imaging is used to visualize directly the transfer of two inner hydrogen atoms in single porphycene molecules. This reaction leads to a chemically equivalent but differently oriented structure and hence results in a rotation of the transition dipole moments. By probing single immobilized molecules with an azimuthally polarized laser beam in the focal spot of a confocal microscope we observe ring-like emission patterns, possible only for a chromophore with two nearly orthogonal transition dipole moments. Numerical simulations of the observed emission patterns yield a value of 72° for the angle between the S0−S1 transition moments in the two tautomeric forms.
Item Type: | Journal article |
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Form of publication: | Publisher's Version |
Faculties: | Chemistry and Pharmacy |
Subjects: | 500 Science > 540 Chemistry |
URN: | urn:nbn:de:bvb:19-epub-14535-6 |
ISSN: | 0002-7863 |
Language: | English |
Item ID: | 14535 |
Date Deposited: | 01. Feb 2013, 14:33 |
Last Modified: | 04. Nov 2020, 12:54 |