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Date: 15-9-2019
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Date: 22-2-2020
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Date: 10-8-2019
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The electrons that surround the nucleus are in motion so they created their own electromagnetic field. This field opposes the the applied magnetic field and so reduces the field experienced by the nucleus. Thus the electrons are said to shield the nucleus. Since the magnetic field experienced at the nucleus defines the energy difference between spin states it also defines what the chemical shift will be for that nucleus. Electron with-drawing groups can decrease the electron density at the nucleus, deshielding the nucleus and result in a larger chemical shift. Compare the data in the table below.
Compound, CH3X | CH3F | CH3OH | CH3Cl | CH3Br | CH3I | CH4 | (CH3)4Si |
Electronegativity of X | 4.0 | 3.5 | 3.1 | 2.8 | 2.5 | 2.1 | 1.8 |
Chemical shift δ (ppm) | 4.26 | 3.4 | 3.05 | 2.68 | 2.16 | 0.23 | 0 |
As can be seen from the data, as the electronegativity of X increases the chemical shift, δ increases. This is an effect of the halide atom pulling the electron density away from the methyl group. This exposes the nuclei of both the C and H atoms, "deshielding" the nuclei and shifting the peak downfield.
The effects are cumulative so the presence of more electron withdrawing groups will produce a greater deshielding and therefore a larger chemical shift, i.e.
Compound | CH4 | CH3Cl | CH2Cl2 | CHCl3 |
δ (ppm) | 0.23 | 3.05 | 5.30 | 7.27 |
These inductive effects are not only felt by the immediately adjacent atoms, but the deshielding can occur further down the chain, i.e.
NMR signal | -CH2-CH2-CH2Br |
δ (ppm) | 1.25 1.69 3.30 |
The π electrons in a compound, when placed in a magnetic field, will move and generate their own magnetic field. The new magnetic field will have an effect on the shielding of atoms within the field. The best example of this is benzene (see the figure below).
This effect is common for any atoms near a π bond, i.e.
Proton Type | Effect | Chemical shift (ppm) |
C6H5-H | highly deshielded | 6.5 - 8 |
C=C-H | deshielded | 4.5 - 6 |
C≡C-H | shielded* | ~2.5 |
O=C-H | very highly deshielded | 9 - 10 |
* the acetylene H is shielded due to its location relative to the π system |
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"عادة ليلية" قد تكون المفتاح للوقاية من الخرف
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ممتص الصدمات: طريقة عمله وأهميته وأبرز علامات تلفه
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المجمع العلمي للقرآن الكريم يقيم جلسة حوارية لطلبة جامعة الكوفة
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