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Photochemistry fluorescence spectroscopy

The metaiioporphyrins form a diverse class of molecules exhibiting complex and varied photochemistries. Until recently time-resolved absorption and fluorescence spectroscopies were the only methods used to study metailoporphyrln excited state relaxation in a submicrosecond regime. In this paper we present the first picosecond time-resolved resonance Raman spectra of excited state metaiioporphyrins outside of a protein matrix. The inherent molecular specificity of resonance Raman scattering provides for a direct probe of bond strengths, geometries, and ligation states of photoexcited metaiioporphyrins. [Pg.266]

Holland, F., U. Aschmutat, M. HeBling, A. Hofzumahaus, and D. H. Ehhalt, Highly Time Resolved Measurements of OH during POPCORN Using Laser-Induced Fluorescence Spectroscopy, in Atmospheric Measurements during POPCORN—Characterization of the Photochemistry over a Rural Area, pp. 205-225, Kluwer Academic, Dordrecht/Norwell, MA, 1998. [Pg.645]

The photochemistry of small molecule LC materials has been an active area of research for many years and has been reviewed recently [9]. The photochemistry of LC polymers, per se, has received much less attention although two brief reviews have appeared [5,10], and there has been a considerable effort to apply some simple photochemical transformations such as trans-cis photoisomerization, to the development of practical devices [1-6]. This section is divided into three parts. In Part A, chromophore aggregation, which seems to be important in almost all the cases in which careful UV-Vis and/or fluorescence studies of films of pure LC polymers have been made, is explicitly discussed. Part B is devoted to a thorough review, organized by chromophore type, of the photochemistry and related photophysics of LC polymers. No attempt has been made to extensively cross-reference the work on LC polymers to the hundreds of papers and reviews on analogous non-LC compounds. However, when it seemed particularly appropriate or interesting, experiments related to optical applications of the photochemistry of LC polymers are briefly described. In Part C, a few experiments are described in which a classical photophysical method, fluorescence spectroscopy, is used to probe the microstructures of some LC polymers. [Pg.136]

Ying, LM, and Xie, XS, Fluorescence spectroscopy, exciton dynamics, and photochemistry of single allophycocyanin triinsis. Journal of Physical Chemistry B102 (1998) 10399-10409. [Pg.95]

Alternatively, during this relatively long lifetime, the molecule can undergo an internal structural change or form new reaction products by an activated collision (photochemistry). This deactivation route is promoted by high light intensities and is used in photochemical synthesis, but it can lead to undesired side effects (e.g.. in fluorescence spectroscopy) because photochemical processes... [Pg.426]

Wardle B (2009) Principles and applications of photochemistry, Wiley. This book includes some excellent chapters on fluorescence sensors and probes, as well as a detailed description of more advanced fluorescence spectroscopy and imaging techniques. [Pg.526]

Mokry M., Gal P, Vidinsky B., Kusnir J., Dubayova K., Mozes S., Sabo J. (2006), In vivo monitoring the changes of interstitial pH and FAD/NADH ratio by fluorescence spectroscopy in healing skin wounds. Photochemistry and Photobiology, 82 pp. 793-797. [Pg.474]

Brancaleon, L. Durkin, A.J. Tu, J.H. Menaker, G. Fallon, J.D Kellias, N., In vivo Fluorescence Spectroscopy of Nonmelanoma Skin Cancer, Photochemistry and Photobiology (2001), 73,178-183. Carden, A. Morris, M.D., Application of Vibrational Spectroscopy to the Study of Mineralized Tissues (Review), J. Biomedical Optics (2000), 5, 259-268. [Pg.146]

Wagnieres G et al. In vivo fluorescence spectroscopy and imaging for oncological applications. Photochemistry and Photobiology 68 603-632, 1998. [Pg.266]

Karatsu, X, Kitamura, A., Zeng, H.L., Arai, T., Sakuragi, H., and Tokumaru, K., Photoisomerization and photocyclization reactions of 1-styrylanthracene, Bull. Chem. Soc. Jpn., 68, 920,1995. Karatsu, X, Itoh, H., Nishigaki, A., Fukui, K., Kitamura, A., Matsuo, S., and Misawa, H., Picosecond time-resolved fluorescence spectroscopy of (Z)-l-(2-anthryl)-2-phenylethene and its model compounds understanding the photochemistry by distinguishing between the s-cis and s-trans rota-mers, J. Phys. Chem. A, 104, 6993, 2000. [Pg.677]

Holden, D. A., Jordan, K., and Safarzadeh-Amiri, A., Studies of polymer photostabihzation using fluorescence spectroscopy photochemistry of naphthyl methacrylate copolymers. Macromolecules, 19, 895,1986. [Pg.828]

Yoshikawa, Hiroyuki and Masuhara, Hiroshi Near-field Fluorescence Spectroscopy and Photochemistry of Organic Mesoscopic Materials in J. of Photochemistry and Photobiology C Photochemistry Reviews 1, 57-78 (2000). [Pg.2964]

The general principle of detection of free radicals is based on the spectroscopy (absorption and emission) and mass spectrometry (ionization) or combination of both. An early review has summarized various techniques to detect small free radicals, particularly diatomic and triatomic species.68 Essentially, the spectroscopy of free radicals provides basic knowledge for the detection of radicals, and the spectroscopy of numerous free radicals has been well characterized (see recent reviews2-4). Two experimental techniques are most popular for spectroscopy studies and thus for detection of radicals laser-induced fluorescence (LIF) and resonance-enhanced multiphoton ionization (REMPI). In the photochemistry studies of free radicals, the intense, tunable and narrow-bandwidth lasers are essential for both the detection (via spectroscopy and photoionization) and the photodissociation of free radicals. [Pg.472]

Spectroscopy and photochemistry of CF3NO in the visible region have been extensively studied by Roellig and Houston (113,114), Bower et al. (115), Jones et al. (116), and Spears and Hoffland (117). Trifluoronitrosomethane has a weak structured absorption spectrum in the visible near 700 nm. Absorption of light in this region induced fluorescence as well as dissociation, which is similar to the H2CO photochemistry in the ultraviolet described earlier. [Pg.29]

Crystal field theory, intensities of 4f-4f transitions, Judd-Ofelt theory of electric-dipole transitions, covalency model of hypersensitivity, dynamic coupling mechanism, solution spectra, spectral data for complexes, solvent effects, fluorescence and photochemistry of lanthanide complexes are dealt with in spectroscopy of lanthanide complexes. [Pg.1000]

Martin CB, Shi X, Tsao M-L, Karweik D, Brooke J, Hadad CM, Platz MS. (2002) The photochemistry of riboflavin tetraacetate and nucleosides. A study using density functional theory, laser flash photolysis, fluorescence, UV-Vis and time resolved infrared spectroscopy. J Phys Chem B 106 10263-10271. [Pg.226]

A brief review and reassessment of data on the photophysics of benzene has been presented by Pereira. Evidence for the l E2g valence state has been obtained by u.v. two-photon spectroscopy.Slow electron impact excites fluorescence in thin films of benzene at 77 K as well as emission from isomers." The fluorescence yields and quenching by chloroform of alkyl-benzenes and 1-methylnaphthalene after excitation into Si, Sz, and S3 states and after photoionization have been measured. The channel-three process has been reconsidered in terms of the effects of local modes and Morse oscillator potentials. Excited-state dipole moments of some monosubstituted benzenes have been estimated from solvent effects on electronic absorption spectra, Structural imperfections influence the photochemistry of durene in crystals at low temperatures. Relaxation time studies on excited oxido-substituted p-oligophenylenes have been made by fluorescence depolarization... [Pg.10]


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See also in sourсe #XX -- [ Pg.394 , Pg.396 ]




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