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Anisotropic Intramolecular Magnetic Fields

The neighbor anisotropy term 7 of eq. (3.2) plays an important role in proton shielding, permitting, for example, a distinct differentiation between aromatic and olefinic protons due to the ring current effect. However, this contribution is small in 13C NMR ( 2 ppm). A comparison of the methyl carbon shieldings in methylcyclohexene and toluene shows that the ring current effect often cannot be clearly separated from other shielding contributions  [Pg.116]

A small ring current was described for 1,4-dodecamethylene benzene [83], The most shielded methylene carbons of this ansa compound shift upheld by 0.7 ppm relative to those in cyclopentadecane  [Pg.117]


Nuclear magnetic resonance (NMR), in particular, deuterium NMR, has proven to be a valuable technique for determining the nature of molecular organization in liquid crystals. The utility of the NMR technique derives from the fact that the relevant NMR interactions are entirely intramolecular, i.e. the dominant interaction is that between the nuclear quadrupole moment of the deuteron and the local electric-field gradient (EFG) at the deuterium nucleus. The EFG tensor is a traceless, axially symmetric, second-rank tensor with its principal component along the C—D bond. In a nematic fluid rapid anisotropic reorientation incompletely averages the quadrupolar interaction tensor q, resulting in a nonzero projection similar to the result in Eq. (5.6) ... [Pg.342]


See other pages where Anisotropic Intramolecular Magnetic Fields is mentioned: [Pg.116]    [Pg.116]    [Pg.633]    [Pg.115]    [Pg.229]    [Pg.110]    [Pg.144]    [Pg.82]    [Pg.29]    [Pg.127]    [Pg.96]    [Pg.130]    [Pg.229]    [Pg.435]    [Pg.52]    [Pg.346]    [Pg.52]    [Pg.514]    [Pg.99]    [Pg.35]    [Pg.635]    [Pg.405]    [Pg.14]   


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Field, intramolecular

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