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Carbon coupling constants ring strain

Carbon-hydrogen spin-spin coupling constants are included in a review by Hansen and discussed in terms of ring strain, steric effects, electronegativity, lone pair effects and electric field effects. Additivity of these effects in a few systems is commented on. [Pg.107]

The C NMR spectrum of cyclobutadiene-iron tricarbonyl consists of a singlet at 209.0 ppm for the carbonyl carbons and a doublet centered at 61.0 ppm, Jc-H = 191 Hz (193). The large C-H coupling constant suggests hybridization at carbon between sp and sp which is consistent with the strained cyclobutadiene ring. In a plot of C versus chemical shifts the cyclobutadiene resonances fall on the same line as resonances for aromatic molecules, their ions and their metal n complexes. [Pg.370]

C-proton coupling constants ( 7) are very dependent on the hybridization of the carbon atom. Strained ring compounds have larger coupling constants because of increased s-character. Reich, Hans J., University of Wisconsin http //www.chem.wise.edu/areas/reich/nmr/06-cnn-05-ljch.htm 7ch. 7ch. Tch coupling constants... [Pg.741]


See other pages where Carbon coupling constants ring strain is mentioned: [Pg.181]    [Pg.172]    [Pg.227]    [Pg.123]    [Pg.81]    [Pg.138]    [Pg.740]    [Pg.1903]    [Pg.31]    [Pg.202]    [Pg.123]    [Pg.740]    [Pg.218]    [Pg.354]    [Pg.187]    [Pg.373]    [Pg.40]    [Pg.301]    [Pg.126]    [Pg.97]    [Pg.411]    [Pg.1903]    [Pg.599]    [Pg.110]    [Pg.1023]   
See also in sourсe #XX -- [ Pg.138 ]




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Carbon coupling

Carbon coupling constants

Ring Carbon

Ring strain

Strain coupling

Strained rings

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