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Hamaguchi Lab.

Spectrophysical Chemistry bridges chemistry and biology

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Time-Resolved Infrared Spectroscopic System (mid wavelength IR) (4000-800cm-1)

Nanosecond Time-resolved Infrared Spectrometer

Nanosecond to microsecond dynamics of photo-excited molecules are detected as temporal changes in infrared absorption spectra. The sensitivity of the system is so high that very small changes in absorbance (ΔA10-6) can be detected.

Fig. 1

Fig. 1. Setup

Molecules are photo-excited by the second harmonic of the output of a Nd:YAG laser pumped dye laser (Fig. 2). The pump laser beamd is overlaped with the infrared probe beam on the sample jet (Fig. 3).

Fig. 2

Fig. 2. Nd:YAG laser & Dye laser

Fig. 3

Fig. 3. Sample Jet

The infrared probe light is dispersed by a monochromator and detected by an MCT detector (Fig. 4).

Fig. 4

Fig. 4. Spectrometer & Detector

Reverse Proton Transfer Reaction in the Ground State of 2-aminopyridine with Acetic Acid Complex

Stepwise double proton transfer takes place in the electronic excited state of 2-aminopyridine-acetic acid complex (Ref. [1]). The reverse proton transfer reaction is observed as the recovery of the bleaching of NH bending band (Fig. 7,8).

Fig. 5

Fig. 5. Proton transfer reactions of 2-amnopyridine-acetic acid complex

Fig. 6

Fig. 6. Time-resolved infrared difference spectra

Fig. 7

Fig. 7. Temporal change in the infrared absorption at 1640cm-1 2-aminopyridine-acetic acid (blue line), 2-aminopyridine monomer (red line)

References

  1. H. Ishikawa, K. Iwata and H. Hamaguchi, J. Phys. Chem., 106, 2305, (2002).
  2. S. Sato, C. Kudo and H. Hamaguchi, proceedings for twelfth Time -Resolved Vibrational Spectroscopy Conference

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