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Correlation spectroscopy , natural

Kogure, T., Karasawa, S., Araki, T., Saito, K., Kinjo, M., and Miyawaki, A. 2006. A fluorescent variant of a protein from the stony coral Montipora facilitates dual-color singlelaser fluorescence cross-correlation spectroscopy. Nature Biotechnol. 24 577-81. [Pg.269]

Bacia, K. and Schwille, P. (2007) Practical guidelines for dual-color fluorescence cross-correlation spectroscopy. Nature Protocols, 2, 2842-2856. [Pg.384]

Up to now it has been tacitly assumed that each molecular motion can be described by a single correlation time. On the other hand, it is well-known, e.g., from dielectric and mechanical relaxation studies as well as from photon correlation spectroscopy and NMR relaxation times that in polymers one often deals with a distribution of correlation times60 65), in particular in glassy systems. Although the phenomenon as such is well established, little is known about the nature of this distribution. In particular, most techniques employed in this area do not allow a distinction of a heterogeneous distribution, where spatially separed groups move with different time constants and a homogeneous distribution, where each monomer unit shows essentially the same non-exponential relaxation. Even worse, relaxation... [Pg.37]

LC-NMR plays a central role in the on-line identification of the constituents of crude plant extracts (Wolfender and others 2003). This technique alone, however, will not provide sufficient spectroscopic information for a complete identification of natural products, and other hyphenated methods, such as LC-UV-DAD and LC-MS/MS, are needed for providing complementary information. Added to this, LC-NMR experiments are time-consuming and have to be performed on the LC peak of interest, identified by prescreening with LC-UV-MS. NMR applied to phenolic compounds includes H NMR,13 C NMR, correlation spectroscopy (COSY), heteronuclear chemical shift correlation NMR (C-H HECTOR), nuclear Overhauser effect in the... [Pg.63]

No general studies have been carried out for these compounds, but there are several reports in which the stereochemistry of the final product has been elucidated by NOESY, correlation spectroscopy (COSY), or heteronuclear single quantum correlation (HSQC) experiments. For example, intensive NOESY experiments were used to establish the exact nature of each of the three cycloadducts 151a-c generated by the cycloaddition of a substituted nitrone to dimethyl (Z)-diethylenedicarboxylate <2000EJ03633>. [Pg.64]

H is particularly important in NMR experiments because of its high sensitivity and natural abundance. For macromolecules, 1H NMR spectra can become quite complicated. Even a small protein has hundreds of 1H atoms, typically resulting in a one-dimensional NMR spectrum too complex for analysis. Structural analysis of proteins became possible with the advent of two-dimensional NMR techniques (Fig. 3). These methods allow measurement of distance-dependent coupling of nuclear spins in nearby atoms through space (the nuclear Overhauser effect (NOE), in a method dubbed NOESY) or the coupling of nuclear spins in atoms connected by covalent bonds (total correlation spectroscopy, or TOCSY). [Pg.138]

H and 13C NMR techniques have widely been used to determine the configuration of new dioxepins and dithiepins and to elucidate the constitution and conformation of new naturally occurring substances. For example, the configuration of oximes 14 was determined by H and 13C correlated spectra, correlation spectroscopy (COSY), nuclear Overhauser enhancement spectroscopy (NOESY), heteronuclear correlation (HETCOR) spectroscopy, and hetero-nuclear multiple bond correlation (E1MBC) spectroscopy <1998CCA557>. [Pg.324]

Filella, M., Zhang, J., Newman, M.E. and Buffie, J. (1997) Analytical applications of photon correlation spectroscopy for size distribution measurements of natural colloidal suspensions capabilities and limitations. Colloids Surf. A Physicochem. Eng. Aspects, 120, 27 16. [Pg.223]

In colloidal suspensions of anisotropic particles, the static structure factor plays a prominent role in particle size analysis. We have used transient electric birefringence (TEB) and electron microscopy, in addition to laser light scattering, to correlate our analysis of particle size distributions of bentonite suspensions. The complementary nature of TEB and photon correlation spectroscopy (PCS) in particle size analysis will be discussed. [Pg.116]

Other strategies that show great promise in reducing NMR acquisition time utilise methods to obtain multiple sets of data from one experiment through a concept known as time-shared evolution. An example of this process that should find utility in natural products elucidation was demonstrated by a pulse sequence called CN-HMBC.93 Traditionally, a separate 13C-HMBC and 15N-HMBC were acquired independently. However, the CN-HMBC allows both 13C- and 15N-HMBC spectra to be obtained simultaneously. By acquiring both data sets simultaneously, an effective 50% time reduction can be achieved.93 This approach has also been demonstrated for a sensitivity-enhanced 2D HSQC-TOCSY (heteronuclear multiple bond correlation total correlation spectroscopy) and HSQMBC (heteronuclear single quantum... [Pg.288]

Despite the high cost of the equipment required and the time taken for sample preparation and spectra acquisition, MAS-HR NMR provides invaluable stmctural information about the species present in a reaction. Only a few milligrams of resin beads are required and they can be recovered as the technique is nondestructive. The complementarity of the technique with other analytical methods is clear MALDl-TOP cannot discriminate among compounds with the same MW and depends on the ionization properties of the resin-bound compound, while PTIR depends on the presence of selected functional groups in the molecule. MAS-HR NMR can be used independently from the nature of the performed reaction and the functional groups formed or lost during the SPS step. Additionally, two-dimensional MAS techniques such as 2D-COSY (correlated spectroscopy) and TOCSY (total correlated spectroscopy) (171) or 2D-SECSY (spin echo correlation spectroscopy) (181) can provide more detailed information that may be useful in specific cases. [Pg.37]

The structures of the natural products, ceratospongamides from marine red alga (Rhodophyta) Ceratodictyon spongiosum, which each consist of two L-phenylalanine residues, one (L-isoleucine)-methyloxazoline residue, one L-proline residue, and one (L-proline)thiazole residue, were established through extensive NMR experiments, including heteronuclear multiple quantum correlation total correlated spectroscopy (HMQC-TOCSY), and... [Pg.652]

Fluorescence correlation spectroscopy in living cells. Nature... [Pg.384]

The nature of thin films may also be influenced by rapid, thermally driven fluctuations in the local density of liquids. Heuberger, Zach and Spencer performed force and refractive index measurements of hexane confined to nanometer thickness using fast spectral correlation spectroscopy, and observed the fluctuations in density. This finding may help explain observations of high surface mobility, anomalously fast selfdiffusion, and apparent solidification in liquid films. [Pg.1842]


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Correlated spectroscopy

Correlation spectroscopy

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