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Nuclear magnetic shielding substituent effects

E. Additivity of Substituent Effects in Nuclear Magnetic Shielding... [Pg.210]

Gutowsky, H.S., McCall, D.W., McGarvey, B.R. and Meyer, L.H. (1952). Electron Distribution in Molecules. I. F Nuclear Magnetic Shielding and Substituent Effects in Some Benzene Derivatives. J.Am.Chem.Soc., 74,4809-4817. [Pg.578]

Nuclear Magnetic Resonance. A definitive review of interproton allylic spin-spin coupling has been made which contains much of relevance to alicyclic systems. Study of the n.m.r. spectra of 36 axially and equatorially substituted cyclo-hexanols has identified some unexpected chemical shift effects. Substituent-dependent additive shielding increments were used successfully to calculate the chemical shift of methine H atoms present, so confirming the observation of some axial H atom shifts at lower fields than the equatorial H atom resonances, i.e. an inversion of the accepted behaviour. [Pg.149]


See other pages where Nuclear magnetic shielding substituent effects is mentioned: [Pg.252]    [Pg.129]    [Pg.1475]    [Pg.172]    [Pg.93]    [Pg.142]    [Pg.901]    [Pg.1252]    [Pg.88]    [Pg.217]    [Pg.212]    [Pg.109]    [Pg.99]    [Pg.244]   
See also in sourсe #XX -- [ Pg.210 , Pg.211 , Pg.212 , Pg.213 ]




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Shielding effectiveness

Shielding substituents

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