7-resolved spectroscopy

ONE-DIMENSIONAL SPIN ECHO EXPERIMENTS AND TWO-DIMENSIONAL 7-RESOLVED SPECTROSCOPY... 

Time-resolved spectroscopy has become an important field from x-rays to the far-IR. Both IR and Raman spectroscopies have been adapted to time-resolved studies. There have been a large number of studies using time-resolved Raman [39], time-resolved resonance Raman [7] and higher order two-dimensional Raman spectroscopy (which can provide coupling infonuation analogous to two-dimensional NMR studies) [40]. Time-resolved IR has probed neutrals and ions in solution [41, 42], gas phase kmetics [42] and vibrational dynamics of molecules chemisorbed and physisorbed to surfaces [44]- Since vibrational frequencies are very sensitive to the chemical enviromnent, pump-probe studies with IR probe pulses allow stmctiiral changes to... 

Homonuclear teclmiques such as J-resolved spectroscopy also exist for rotatmg all multiplets tlirough 90°, to resolve overlaps and also give a ID spectrum from which all homonuclear couplings have been removed [26]. 

So far we have exclusively discussed time-resolved absorption spectroscopy with visible femtosecond pulses. It has become recently feasible to perfomi time-resolved spectroscopy with femtosecond IR pulses. Flochstrasser and co-workers [M, 150. 151. 152. 153. 154. 155. 156 and 157] have worked out methods to employ IR pulses to monitor chemical reactions following electronic excitation by visible pump pulses these methods were applied in work on the light-initiated charge-transfer reactions that occur in the photosynthetic reaction centre [156. 157] and on the excited-state isomerization of tlie retinal pigment in bacteriorhodopsin [155]. Walker and co-workers [158] have recently used femtosecond IR spectroscopy to study vibrational dynamics associated with intramolecular charge transfer these studies are complementary to those perfomied by Barbara and co-workers [159. 160], in which ground-state RISRS wavepackets were monitored using a dynamic-absorption technique with visible pulses. 

Because this problem is complex several avenues of attack have been devised in the last fifteen years. A combination of experimental developments (protein engineering, advances in x-ray and nuclear magnetic resonance (NMR), various time-resolved spectroscopies, single molecule manipulation methods) and theoretical approaches (use of statistical mechanics, different computational strategies, use of simple models) [5, 6 and 7] has led to a greater understanding of how polypeptide chains reach the native confonnation. 

Relaxation kinetics may be monitored in transient studies tlirough a variety of metliods, usually involving some fonn of spectroscopy. Transient teclmiques and spectrophotometry are combined in time resolved spectroscopy to provide botli tire stmctural infonnation from spectral measurements and tire dynamical infonnation from kinetic measurements that are generally needed to characterize tire mechanisms of relaxation processes. The presence and nature of kinetic intennediates, metastable chemical or physical states not present at equilibrium, may be directly examined in tliis way. 

Pulsed spark sources, in which the material to be analyzed is part of one electrode, are used for semiquantitative analyses. The numerous and complex processes involved in spark discharges have been studied in detail by time- and space-resolved spectroscopy (94). The temperature of d-c arcs, into which the analyte is introduced as an aerosol in a flowing carrier gas, eg, argon, is approximately 10,000 K. Numerous experimental and theoretical studies of stabilized plasma arcs are available (79,95). 

Hydrogen transfer in excited electronic states is being intensively studied with time-resolved spectroscopy. A typical scheme of electronic terms is shown in fig. 46. A vertical optical transition, induced by a picosecond laser pulse, populates the initial well of the excited Si state. The reverse optical transition, observed as the fluorescence band Fj, is accompanied by proton transfer to the second well with lower energy. This transfer is registered as the appearance of another fluorescence band, F2, with a large anti-Stokes shift. The rate constant is inferred from the time dependence of the relative intensities of these bands in dual fluorescence. The experimental data obtained by this method have been reviewed by Barbara et al. [1989]. We only quote the example of hydrogen transfer in the excited state of... 

Figure 5.7 (A) Pulse sequence for gated decoupled /-resolved spectroscopy. It involves decoupling only during the first half of the evolution period

Figure 5.9 Pulse sequence for spin-flip heteronuclear /-resolved spectroscopy.

The pulse sequence used in homonuclear 2D y-resolved spectroscopy is shown in Fig. 5.18. Let us consider a proton, A, coupled to another proton, X. The 90° pulse bends the magnetization of proton A to the y -axis. During the first half of the evolution period, the two vectors (faster... 

Figure 5.18 (A) Pulse sequence for homonuclear 2D y-resolved spectroscopy. (B) Effect of 90° H and 180° H pulses on an H doublet. (C) In the absence of coupling, the vectors are refocused by the 180° H pulse after t. This serves to remove any field inhomogeneities or chemical shift differences.

What is the difference between homo- and heteronuclear 2D /-resolved spectroscopy ... 

In the previous section we were concerned with 2D /-resolved spectroscopy i.e., chemical shifts of the nuclei were presented along one axis and their couplings along the other axis. The data thus obtained provided information about multiplicity. 

A more useful type of 2D NMR spectroscopy is shift-correlated spectroscopy (COSY), in which both axes describe the chemical shifts of the coupled nuclei, and the cross-peaks obtained tell us which nuclei are coupled to which other nuclei. The coupled nuclei may be of the same type—e.g., protons coupled to protons, as in homonuclear 2D shift-correlated experiments—or of different types—e.g., protons coupled to C nuclei, as in heteronuclear 2D shift-correlated spectroscopy. Thus, in contrast to /-resolved spectroscopy, in which the nuclei were being modulated (i.e., undergoing... 

A consistent picture for dynamics of heterogeneous ET has been emerging in the last 5 years with the development of new experimental approaches. Techniques such as AC impedance, modulated and time-resolved spectroscopy, SECM, and photoelectrochemical methods have extended our knowledge of charge-transfer kinetics to a wide range of time scales. This can be exemplified by comparing impedance analysis, which is limited to k of... 

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