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Quanta ray mopo sl

Manufactured by Spectra-Physics

The Quanta-Ray MOPO-SL is a laboratory equipment product manufactured by Spectra-Physics. It is a tunable optical parametric oscillator (OPO) that generates coherent light over a wide range of wavelengths. The core function of the Quanta-Ray MOPO-SL is to provide a versatile light source for various applications in scientific research and industrial settings.

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5 protocols using quanta ray mopo sl

1

Tunable Light Irradiation of Cryogenic Matrices

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The matrices
were irradiated through the outer KBr window of the cryostat, using
tunable narrow-band light with a full width at half-maximum (fwhm)
of ∼0.2 cm–1, provided by a signal (visible
light) or a frequency-doubled signal (UV range) beam of an optical
parametric oscillator (Spectra Physics Quanta-Ray MOPO-SL) pumped
with a pulsed Nd:YAG laser (Spectra-Physics PRO-230: output power
≈4.3 W; wavelength = 355 nm; duration = 10 ns; repetition rate
= 10 Hz).
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2

Matrix-Isolation Photochemical Reactions

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The matrix-isolated species were irradiated (through the outer quartz window of the cryostat) using tunable narrowband (∼0.2 cm -1 spectral width) light provided by a Spectra Physics Quanta-Ray MOPO-SL optical parametric oscillator (OPO) pumped with a pulsed Nd:YAG laser (repetition rate = 10 Hz, duration = 10 ns). For UV-irradiations the frequency-doubled beam (signal or idler) was used (pulse energy ∼1 mJ). For Vis-irradiations the signal beam was used (pulse energy ∼10 mJ). For near-IR-irradiations the idler beam was used (pulse energy ∼10 mJ).
The outcome of those irradiations (consumption of a reactant and generation of a photoproduct) was monitored by collecting IR spectra.
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3

Pulsed Laser-Driven OPO Irradiation

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The Journal of Physical Chemistry parametric oscillator (OPO, Spectra Physics Quanta-Ray MOPO-SL) pumped by a pulsed Nd:YAG laser (duration: 10 ns; repetition rate: 10 Hz). Irradiation experiments in the near-IR region were performed using frequency-tunable narrowband light (~0.2 cm -1 spectral width; 100 mW) generated by the idler beam of the same OPO-laser system.
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4

Matrix-Isolated Samples Irradiation

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The matrix-isolated samples were irradiated at the frequency of the second OH stretching overtones using two monochromatic near-IR light sources: (i) tunable near-IR light (full range) generated as the idler beam of a Spectra Physics Quanta-Ray MOPO-SL optical parametric oscillator (fwhm 0.2 cm À1 , pulse energy 10 mJ), pumped with a pulsed Nd:YAG laser (10 ns, repetition rate 10 Hz), and (ii) tunable near-IR light (B10 500-10 100 cm À1 ) generated by a continuous wave diode laser Toptica DLC TA PRO (fwhm o1 MHz, up to 3 W). In a typical experiment, irradiation was carried out for 20 min using 120 mW of power. Similar results were obtained using both near-IR light sources.
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5

Cryogenic Matrix Infrared Spectroscopy

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Commercial AB (Fluka, purity 98%), DAB (Sigma-Aldrich, purity 97%), and AT (Sigma-Aldrich, 98%) were placed in a glass tube connected to the vacuum chamber of the cryostat through a shutoff valve. The compound vapors were deposited with a large excess of the matrix gas (argon N60 or xenon N48, Air Liquide) onto a CsI substrate cooled using a closed-cycle helium refrigerator (APD Cryogenics DE-202A). The deposition temperature was 15 and 30 K for argon and xenon matrices, respectively. The infrared spectra were recorded in the 4000-400 cm À1 range with 0.5 cm À1 resolution using a Nicolet 6700 FTIR spectrometer equipped with DTGS and MCT-B detectors and a Ge/KBr beam splitter. The matrices were irradiated through a quartz window of the cryostat using tunable narrowband (0.2 cm À1 spectral width) light provided by a Spectra Physics Quanta-Ray MOPO-SL optical parametric oscillator (OPO) pumped with a pulsed Nd:YAG laser (repetition rate = 10 Hz, duration B10 ns). In the visible range (440-600 nm), the signal beam of the OPO was used (pulse energy of B30-40 mJ). In the UV range (230-440 nm), the frequency-doubled signal or idler beam was used (pulse energy of B3 mJ). The selection of the irradiation wavelengths was guided by the absorption spectra of the compounds in solution (Fig. S2,ESI †).
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