4.6 Article

Probing Organometallic Reactions by Time-Resolved Infrared Spectroscopy in Solution and in the Solid State Using Quantum Cascade Lasers

Journal

APPLIED SPECTROSCOPY
Volume 69, Issue 5, Pages 519-524

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1366/14-07708

Keywords

Quantum cascade laser; QCL; Photochemistry; Time-resolved; Infrared; TRIR

Funding

  1. EPSRC
  2. Royal Society Wolfson Merit Award

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The photochemistry and photophysics of metal carbonyl compounds (W(CO)(6), Cp*Rh(CO)(2) (Cp* = eta(5)-C5Me5), and fac-[Re(CO)(3)(4,4'-bpy)(2)Br] [bpy = bipyridine]) have been examined on the nanosecond timescale using a time-resolved infrared spectrometer with an external cavity quantum cascade laser (QCL) as the infrared source. We show the photochemistry of W(CO)(6) in alkane solution is easily monitored, and very sensitive measurements are possible with this approach, meaning it can monitor small transients with absorbance changes less than 10(-6) Delta OC. The C-H activation of Cp*Rh(CO)(C6H12) to form Cp*Rh(CO)(C6H11)H occurs within the first few tens of nanoseconds following photolysis, and we demonstrate that kinetics obtained following deconvolution are in excellent agreement with those measured using an ultrafast laser-based spectrometer. We also show that the high flux and tunability of QCLs makes them suited for solid-state and time-resolved measurements.

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