Time-resolved infrared spectroscopy transients

Dyer R B, Einarsdottir 6, Killough P M, Lopez-Garriga J J and Woodruff W H 1989 Transient binding of photodissociated CO to of eukaryotic cytochrome oxidase at ambient temperature. Direct evidence from time-resolved infrared spectroscopy J. Am. Chem. Soc. Ill 7657-9... 

Despite the considerable amount of information that has been garnered from more traditional methods of study it is clearly desirable to be able to generate, spectroscopically characterize and follow the reaction kinetics of coordinatively unsaturated species in real time. Since desired timescales for reaction will typically be in the microsecond to sub-microsecond range, a system with a rapid time response will be required. Transient absorption systems employing a visible or UV probe which meet this criterion have been developed and have provided valuable information for metal carbonyl systems [14,15,27]. However, since metal carbonyls are extremely photolabile and their UV-visible absorption spectra are not very structure sensitive, the preferred choice for a spectroscopic probe is time resolved infrared spectroscopy. Unfortunately, infrared detectors are enormously less sensitive and significantly slower... 

These conclusions were supported by transient absorption spectroscopy, which revealed signals corresponding to the formation of the diimine radical anion, with lifetimes in close agreement with the luminescence lifetimes. Time-resolved infrared spectroscopy of the acetylide C = C bonds provides further conclusive evidence for the MLCT assignment. Thus, in the ground state IR spectrum of 4, there are two v(C=C) bands at 2115 and 2124 cm-1, whilst the step-scan FTIR difference spectrum obtained 50 ns after irradiation at 355 nm reveals bleaching of the parent bands, and the formation... 

The detection of short-lived transient species is often achieved by flash photolysis where an extremely short flash of UV/Vis radiation from a laser generates a high concentration of transient species, and a second probe beam monitors any changes that occur after the flash. Traditionally, UVA is spectroscopy has been used as a detection method. However, time-resolved infrared spectroscopy (TRIR), a combination of UV flash photolysis and fast IR detection, also has a long history. There are several different approaches to fast IR spectroscopy and the method of choice depends upon the timescale of the reaction. Measurements on the nanosecond to millisecond timescale are obtained using point-by-point techniques or by step-scan FTIR. In the point-by-point approach, a continuous wave IR laser (GO or diode) or globar is used as the IR source, which is tuned to one particular IR frequency (Figure 3). ... 

Laser flash photolysis methods have also been applied to the study of nitrenium ion trapping rates and hfetimes. This method relies on short laser pulses to create a high transient concentration of the nitrenium ion, and fast detection technology to characterize its spectrum and lifetime The most frequently used detection method is fast UV-vis spectroscopy. This method has the advantage of high sensitivity, but provides very little specific information about the structure of the species being detected. More recently, time-resolved infrared (TRIR) and Raman spectroscopies have been used in conjunction with flash photolysis methods. These provide very detailed structural information, but suffer from lower detection sensitivity. 

The IR spectra of carbazole and carbazole-(H20) ( =l-3) clusters in a supersonic jet, measured by IR dip spectroscopy, show vibrational structures of both the monomer and the clusters in the 2900-3800 cm frequency region, assigned to the NH stretch of carbazole and the OH stretches of H2O molecules in the clusters <2001PCA8651>. In the first excited singlet and triplet states A -(4-cyanophenyl)carbazole gives rise to transient bands at 2090 cm and 2060 cm detected by time-resolved infrared absorption spectroscopy and attributed to the CN stretch modes of the molecule <2002CL340>. 

Transient terahertz spectroscopy Time-resolved terahertz (THz) spectroscopy (TRTS) has been used to measure the transient photoconductivity of injected electrons in dye-sensitised titanium oxide with subpicosecond time resolution (Beard et al, 2002 Turner et al, 2002). Terahertz probes cover the far-infrared (10-600 cm or 0.3-20 THz) region of the spectrum and measure frequency-dependent photoconductivity. The sample is excited by an ultrafast optical pulse to initiate electron injection and subsequently probed with a THz pulse. In many THz detection schemes, the time-dependent electric field 6 f) of the THz probe pulse is measured by free-space electro-optic sampling (Beard et al, 2002). Both the amplitude and the phase of the electric field can be determined, from which the complex conductivity of the injected electrons can be obtained. Fitting the complex conductivity allows the determination of carrier concentration and mobility. The time evolution of these quantities can be determined by varying the delay time between the optical pump and THz probe pulses. The advantage of this technique is that it provides detailed information on the dynamics of the injected electrons in the semiconductor and complements the time-resolved fluorescence and transient absorption techniques, which often focus on the dynamics of the adsorbates. A similar technique, time-resolved microwave conductivity, has been used to study injection kinetics in dye-sensitised nanocrystalline thin films (Fessenden and Kamat, 1995). However, its time resolution is limited to longer than 1 ns. 

Once the transient species has been formed, it has to be monitored by some form of kinetic spectroscopy, typically with ultraviolet-visible absorption or emission, infrared (time-resolved infrared or TRIR) (74), or resonance Raman (time-resolved resonance Raman or TR3) (80) methods of detection. The transient is usually tracked by a probe beam at a single characteristic frequency, thereby giving direct access to the kinetic dimension. Spectra can then be built up point by point, if necessary, with an appropriate change of probe frequency for each point, although improvements in the sensitivity of multichannel detectors may be expected to lead increasingly to the replacement of the laborious point-by-point method by full two-dimensional methods of spectroscopic assay (that is, with both spectral and kinetic dimensions). 

Another method, which allows the structural characterization and elucidation of the reactivity of transient species using infrared spectroscopy, is to observe them in real time, using fast time-resolved infrared (TRIR) spectroscopy. In this section we shall focus on the application of fast (submillisecond) and ultrafast (subnanosecond) TRIR spectroscopy to coordination compounds, and describe experiments that cannot be performed using conventional infrared spectrometers. 

TA transient absorbance TRIR time-resolved infrared resonance TRFS time-resolved fluorescence spectroscopy. 

Reports of new tungsten complexes include the reaction of the transient species W(CO)5(cyclohexane) with cyclo-C4H 0 (n = 4, 6, 8) studied by time-resolved infrared absorption spectroscopy. Schultz and co-workers have noted an unusual solvent isotope effect in the reaction of W(CO)5(solv) (solv = cyclohexane or cyclohexane-rfu) with TFIF. Some interesting chemistry involving W(CO)5(2,5-dihydrofuran) is noted by the same group. Adducts of cyclotriphosphorus complexes have been reported by Di Vaira and co-workers, leading to the synthesis, solid state structure and solution behaviour of the bis-adducts [ (MeC(CH2PPh2)3)Co (P3)(M(CO)5 2], where M is a Group 6 metal. 

Probing Metalloproteins Electronic absorption spectroscopy of copper proteins, 226, 1 electronic absorption spectroscopy of nonheme iron proteins, 226, 33 cobalt as probe and label of proteins, 226, 52 biochemical and spectroscopic probes of mercury(ii) coordination environments in proteins, 226, 71 low-temperature optical spectroscopy metalloprotein structure and dynamics, 226, 97 nanosecond transient absorption spectroscopy, 226, 119 nanosecond time-resolved absorption and polarization dichroism spectroscopies, 226, 147 real-time spectroscopic techniques for probing conformational dynamics of heme proteins, 226, 177 variable-temperature magnetic circular dichroism, 226, 199 linear dichroism, 226, 232 infrared spectroscopy, 226, 259 Fourier transform infrared spectroscopy, 226, 289 infrared circular dichroism, 226, 306 Raman and resonance Raman spectroscopy, 226, 319 protein structure from ultraviolet resonance Raman spectroscopy, 226, 374 single-crystal micro-Raman spectroscopy, 226, 397 nanosecond time-resolved resonance Raman spectroscopy, 226, 409 techniques for obtaining resonance Raman spectra of metalloproteins, 226, 431 Raman optical activity, 226, 470 surface-enhanced resonance Raman scattering, 226, 482 luminescence... 

Selected entries from Methods in Enzymology [vol, page(s)] Biomolecular vibrational spectroscopy, 246, 377 Raman spectroscopy of DNA and proteins, 246, 389 resonance Raman spectroscopy of metalloproteins, 246, 416 structure and dynamics of transient species using time-resolved resonance Raman spectroscopy, 246, 460 infrared spectroscopy applied to biochemical and biological problems, 246, 501 resonance Raman spectroscopy of quinoproteins, 258, 132. 

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