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Raman near-infrared

D. Lipp and A.L. Smith, In A. Lee Smith (Ed.), The Analytical Chemistry of Silicones, Infrared, Raman, near-infrared and ultraviolet spectroscopy, John Wiley and Sons Ltd, New York, 1991, Ch. 11, pp. 305-346. [Pg.254]

R Musto, M. Abbate, G. Ragosta and G. Scarinzi, A smdy by Raman, near-infrared and dynamic-mechanical spectroscopies on the curing behaviour, molecular structure and viscoelastic properties of epoxy/anhydride networks, Polymer, 48, 3703-3716 (2007). [Pg.240]

Stichtemath, A., R. Schweitzer-Stenner, W. Dreybrodt, R.S.W. Mak, X-Y. Li, L.D. Sparks, J.A. Shelnutt, C.J. Medforth, and K.M. Smith (1993). Macrocycle and substituent vibrational modes of nonplanar nickel(II) octaethyltetraphenylporphyrin from its resonance Raman, near-infrared-excited FT Raman, and FT-IR spectra and deuterium isotope shifts. J. Phys. Chem. 97, 3701. [Pg.793]

E. D. Lipp, A. L. Smith, Infrared, Raman, Near-Infrared, and Ultraviolet Spectroscopy, in The Analytical Chemistry of Silicones, Chemical Analysis Series, Vol. 112 (Ed. A. L. Smith), John Wiley, New York, 1991, p. 305. [Pg.149]

Continuous wave (CW) lasers such as Ar and He-Ne are employed in conmionplace Raman spectrometers. However laser sources for Raman spectroscopy now extend from the edge of the vacuum UV to the near infrared. Lasers serve as an energetic source which at the same hme can be highly monochromatic, thus effectively supplying the single excitation frequency, v. The beams have a small diameter which may be... [Pg.1199]

Kneipp K, Kneipp H and Seifert F 1994 Near-infrared excitation profile study of surface-enhanced hyper-Raman scattering and surface-enhanced Raman scattering by means of tunable mode-locked... [Pg.1231]

Kneipp K, Kneipp H, Deinum G, Itzkan I, Dasari R R and Feld M S 1998 Single-molecule detection of a cyanine dye in silver colloidal solution using near-infrared surface-enhanced Raman scattering App/. Spectrosc. 52 175-8... [Pg.2506]

Wang C, Mohney B K, Williams R, Hupp J T and Walker G C 1998 Solvent control of vibronic coupling upon intervalence charge transfer excitation of (NC)gFeCNRu(NH3)g- as revealed by resonance Raman and near-infrared absorption spectroscopies J. Am. Chem. Soc. 120 5848-9... [Pg.2995]

Another method, called photobleaching, works on robust soHds but may cause photodecomposition in many materials. The simplest solution to the fluorescence problem is excitation in the near infrared (750 nm—1.06 pm), where the energy of the incident photons is lower than the electronic transitions of most organic materials, so fluorescence caimot occur. The Raman signal can then be observed more easily. The elimination of fluorescence background more than compensates for the reduction in scattering efficiency in the near infrared. Only in the case of transition-metal compounds, which can fluoresce in the near infrared, is excitation in the midvisible likely to produce superior results in practical samples (17). [Pg.210]

Lasers having wavelengths ranging from the deep uv to the near infrared have been used in Raman spectroscopy. In industrial laboratories, the most common laser is the Nd YAG operating at 1.06 pm. Increasingly, diode lasers or other lasers operating in the 750—785-nm region are encountered. These... [Pg.210]

Infrared Spectrophotometry. The isotope effect on the vibrational spectmm of D2O makes infrared spectrophotometry the method of choice for deuterium analysis. It is as rapid as mass spectrometry, does not suffer from memory effects, and requites less expensive laboratory equipment. Measurement at either the O—H fundamental vibration at 2.94 p.m (O—H) or 3.82 p.m (O—D) can be used. This method is equally appticable to low concentrations of D2O in H2O, or the reverse (86,87). Absorption in the near infrared can also be used (88,89) and this procedure is particularly useful (see Infrared and raman spectroscopy Spectroscopy). The D/H ratio in the nonexchangeable positions in organic compounds can be determined by a combination of exchange and spectrophotometric methods (90). [Pg.9]

Advanced techniques like molecularly imprinted polymers (MIPs), infrared/near infrared spectroscopy (FT-IR/NIR), high resolution mass spectrometry, nuclear magnetic resonance (NMR), Raman spectroscopy, and biosensors will increasingly be applied for controlling food quality and safety. [Pg.314]

Figure 2.9 Spectra of a single adenine nanocrystal, (a) TERS spectrum, (b) ordinal SERS spectrum, and (c) ordinary near-infrared (NIR) Raman spectra. For the SERS measurement, a silver island film was used. For the NIR Raman measurement, i thick sample of adenine was used with a 1 h exposure. Figure 2.9 Spectra of a single adenine nanocrystal, (a) TERS spectrum, (b) ordinal SERS spectrum, and (c) ordinary near-infrared (NIR) Raman spectra. For the SERS measurement, a silver island film was used. For the NIR Raman measurement, i thick sample of adenine was used with a 1 h exposure.
Raman spectroscopy has enjoyed a dramatic improvement during the last few years the interference by fluorescence of impurities is virtually eliminated. Up-to-date near-infrared Raman spectrometers now meet most demands for a modern analytical instrument concerning applicability, analytical information and convenience. In spite of its potential abilities, Raman spectroscopy has until recently not been extensively used for real-life polymer/additive-related problem solving, but does hold promise. Resonance Raman spectroscopy exhibits very high selectivity. Further improvements in spectropho-tometric measurement detection limits are also closely related to advances in laser technology. Apart from Raman spectroscopy, areas in which the laser is proving indispensable include molecular and fluorescence spectroscopy. The major use of lasers in analytical atomic... [Pg.734]


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