One-Color Reversible Control of Photochromic Reactions in a Diarylethene Derivative: Three-Photon Cyclization and Two-Photon Cycloreversion by a Near-Infrared Femtosecond Laser Pulse at 1.28 μm
Photons
Molecular Structure
Cyclization
Infrared Rays
Photochemistry
Lasers
Stereoisomerism
Ethylenes
01 natural sciences
0104 chemical sciences
DOI:
10.1021/ja108992t
Publication Date:
2011-02-04T16:16:51Z
AUTHORS (11)
ABSTRACT
One-color control of colorization/decolorization reactions of diarylethene molecules was attained by using nonresonant high-order multiphoton absorption processes with a near-infrared (NIR) femtosecond laser pulse at 1.28 μm with 35 fs full width at half-maximum (fwhm). The intensity of a rather weak laser pulse (<1 nJ/pulse) can induce the simultaneous three-photon absorption leading to the colorization, while much weaker intensity induces two-photon absorption resulting in the decolorization. The spatial patterning concomitant with higher-order multiphoton absorption processes was also demonstrated.
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