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Nuclear enhanced

INEPT-INADEQUATE insensitive nuclear enhancement by polarization transfer... [Pg.290]

INEPT = Intensive Nuclear Enhancement by Polarization Transfer LHRH = Lutenizing Hormone Releasing Hormone M = Monomer... [Pg.142]

Morris G A and Freeman R 1979 Enhancement of nuclear magnetic resonance signals by polarization transfer J. Am. Chem. See. 101 760-2... [Pg.1464]

Ward H R and Lawler R G 1967 Nuclear magnetic resonance emission and enhanced absorption In rapid organometalllc reactions J. Am. Chem. Soc. 89 5518-19... [Pg.1618]

As early as 1889 Walker (320), using samples of thiazole, 2,4-dimethylthiazoie, pyridine, and 2,6-dimethylpyridine obtained from Hantzsch s laboratory, measured the electrical conductivity of their chlorhydrates and compared them with those of salts of other weak bases, especially quinoline and 2-methylquinoline. He observed the following order of decreasing proton affinity (basicity) quinaldine>2,6-dimethyl-pyridine>quinoline>pyridine>2,4-dimethylthiazole> thiazole, and concluded that the replacement of a nuclear H-atom by a methyl group enhanced the basicity of the aza-aromatic substrates. [Pg.91]

Cardiac nuclear imaging using Tc -red blood cells can measure the fraction of blood pumped by the heart during each beat. Tc -DTPA and sodium (9-iodohippurate, C H INNaO, are used to measure renal function of the kidney. The enhanced or diminished uptake of... [Pg.57]

Nuclear Overhauser enhancement (NOE) spectroscopy has been used to measure the through-space interaction between protons at and the protons associated with the substituents at N (20). The method is also useful for distinguishing between isomers with different groups at and C. Reference 21 contains the chemical shifts and coupling constants of a considerable number of pyrazoles with substituents at N and C. NOE difference spectroscopy ( H) has been employed to differentiate between the two regioisomers [153076 5-0] (14) and [153076 6-1] (15) (22). N-nmr spectroscopy also has some utility in the field of pyrazoles and derivatives. [Pg.308]

The specific role of vitamin A in tissue differentiation has been an active area of research. The current thinking, developed in 1979, involves initial dehvery of retinol by holo-B >V (retinol-binding protein) to the cell cytosol (66). Retinol is then ultimately oxidized to retinoic acid and binds to a specific cellular retinoid-binding protein and is transported to the nucleus. Retinoic acid is then transferred to a nuclear retinoic acid receptor (RAR), which enhances the expression of a specific region of the genome. Transcription occurs and new proteins appear during the retinoic acid-induced differentiation of cells (56). [Pg.103]

N-protonation the absolute magnitude of the Ad values is larger than for Af-methylation <770MR(9)53>. Nuclear relaxation rates of and have been measured as a function of temperature for neat liquid pyridazine, and nuclear Overhauser enhancement has been used to separate the dipolar and spin rotational contributions to relaxation. Dipolar relaxation rates have been combined with quadrupole relaxation rates to determine rotational correlation times for motion about each principal molecular axis (78MI21200). NMR analysis has been used to determine the structure of phenyllithium-pyridazine adducts and of the corresponding dihydropyridazines obtained by hydrolysis of the adducts <78RTC116>. [Pg.8]

The main contribution to the spin-lattice relaxation of C nuclei which are connected to hydrogen is provided by the dipole-dipole interaction (DD mechanism, dipolar relaxation). For such C nuclei a nuclear Overhauser enhancement of almost 2 will be observed during H broadband decoupling according to ... [Pg.65]

The difference between 2-CH2 and 6-CH2 is shown by the nuclear Overhauser enhancement (NOE) on the proton at Su = 6.67, if the methylene protons at 5 = 2.87 are irradiated. The assignment of the methylene C atoms can be read from the CH COSY segment. The C atoms which are in close proximity to one another at 5c = 113.3 and 113.8 belong to C-5 and C-7. Carbon atom C-5 is distinguished from C-7 by the pseudo-quartet splitting CJqh = 3.4 Hz to 1-H and A-H2) that involves the methylene group in the ortho position. [Pg.204]

In decoupling the methyl protons, the NOE difference spectrum shows a nuclear Overhauser enhancement on the cyclopropane proton at = 1.60 and on the terminal vinyl proton with trans coupling at <5// = 5.05 and, because of the geminal coupling, a negative NOE on the other terminal proton at Sh= 4.87. This confirms the trans configuration G. In the cis isomer H no NOE would be expected for the cyclopropane proton, but one would be expected for the alkenyl-// in the a-position indicated by arrows in H. [Pg.209]

Safety Monitor is an interactive computer program (Stamm, 1996) that performs real-time assessments of configuration-specific plant accident risk. Originally used at Southern California Edison s San Onofre station in 1994, further development was sponsored by three nuclear utilities and EPRI, to include shutdown operation and expanded user features. It will be enhanced to calculate large early release frequency (a Level 2 risk). [Pg.146]


See other pages where Nuclear enhanced is mentioned: [Pg.272]    [Pg.1309]    [Pg.297]    [Pg.80]    [Pg.272]    [Pg.1309]    [Pg.297]    [Pg.80]    [Pg.1510]    [Pg.1579]    [Pg.2962]    [Pg.490]    [Pg.524]    [Pg.8]    [Pg.226]    [Pg.227]    [Pg.138]    [Pg.329]    [Pg.123]    [Pg.385]    [Pg.400]    [Pg.182]    [Pg.231]    [Pg.239]    [Pg.148]    [Pg.396]    [Pg.473]    [Pg.81]    [Pg.394]    [Pg.59]    [Pg.221]    [Pg.397]    [Pg.165]    [Pg.191]    [Pg.10]    [Pg.237]    [Pg.488]    [Pg.281]    [Pg.670]    [Pg.205]   
See also in sourсe #XX -- [ Pg.381 , Pg.382 ]




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