DETERMINACIÓN DE ESTRUCTURAS ORGÁNICAS (ORGANIC SPECTROSCOPY) · DETERMINACIÓN DE ESTRUCTURAS...
Transcript of DETERMINACIÓN DE ESTRUCTURAS ORGÁNICAS (ORGANIC SPECTROSCOPY) · DETERMINACIÓN DE ESTRUCTURAS...
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DETERMINACIÓN DE ESTRUCTURAS ORGÁNICAS(ORGANIC SPECTROSCOPY)
IR SPECTROSCOPY
Hermenegildo García GómezHermenegildo García GómezDepartamento de QuímicaDepartamento de Química
Instituto de Tecnología QuímicaInstituto de Tecnología QuímicaUniversidad Politécnica de ValenciaUniversidad Politécnica de Valencia
46022 Valencia46022 Valencia
EE--mail: mail: [email protected]@qim.upv.esTelephone: +34 96 387 7807 or ext. 78572/73441Telephone: +34 96 387 7807 or ext. 78572/73441
Fax: + 34 96 387 7809Fax: + 34 96 387 7809
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IR spectroscopyThe Spectrum and Molecular Effects
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IR spectroscopy
The IR Region
• Just below red in the visible region.• Wavelengths usually 2.5-25 µm.• More common units are wavenumbers,
or cm-1, the reciprocal of the wavelength in centimeters.
• Wavenumbers are proportional to frequency and energy. =>
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IR spectroscopyMolecular Vibrations
Covalent bonds vibrate at only certain allowable frequencies.
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IR spectroscopyStretching Frequencies
• Frequency decreases with increasing atomic weight.
• Frequency increases with increasing bond energy. =>
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IR spectroscopy
Vibrational Modes
Nonlinear molecule with n atoms usually has 3n - 6 fundamental vibrational modes.
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IR spectroscopy
Fingerprint of Molecule
• Whole-molecule vibrations and bending vibrations are also quantitized.
• No two molecules will give exactly the same IR spectrum (except enantiomers).
• Simple stretching: 1600-3500 cm-1.• Complex vibrations: 600-1400 cm-1,
called the “fingerprint region.”=>
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IR spectroscopy
IR-Active and Inactive• A polar bond is usually IR-active.• A nonpolar bond in a symmetrical
molecule will absorb weakly or not at all.
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IR spectroscopyAn Infrared Spectrometer
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IR spectroscopy
FT-IR Spectrometer
• Uses an interferometer.• Has better sensitivity.• Less energy is needed from source.• Completes a scan in 1-2 seconds.• Takes several scans and averages them.• Has a laser beam that keeps the
instrument accurately calibrated. =>
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IR spectroscopyCarbon-Carbon Bond Stretching
• Stronger bonds absorb at higher frequencies:ØC-C 1200 cm-1
ØC=C 1660 cm-1
ØC≡C 2200 cm-1 (weak or absent if internal)• Conjugation lowers the frequency:Øisolated C=C 1640-1680 cm-1
Øconjugated C=C 1620-1640 cm-1
Øaromatic C=C approx. 1600 cm-1 =>
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IR spectroscopyCarbon-Hydrogen Stretching
Bonds with more s character absorb at a higher frequency.Øsp3 C-H, just below 3000 cm-1 (to the right)Øsp2 C-H, just above 3000 cm-1 (to the left)Øsp C-H, at 3300 cm-1
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IR spectroscopy
An Alkane IR Spectrum
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IR spectroscopy
An Alkene IR Spectrum
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IR spectroscopyAn Alkyne IR Spectrum
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IR spectroscopyO-H and N-H Stretching
• Both of these occur around 3300 cm-1, but they look different.ØAlcohol O-H, broad with rounded tip.ØSecondary amine (R2NH), broad with one
sharp spike.ØPrimary amine (RNH2), broad with two
sharp spikes.ØNo signal for a tertiary amine (R3N) =>
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IR spectroscopyAn Alcohol IR Spectrum
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IR spectroscopyAn Amine IR Spectrum
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IR spectroscopy
Carbonyl Stretching
• The C=O bond of simple ketones, aldehydes, and carboxylic acids absorb around 1710 cm-1.
• Usually, it’s the strongest IR signal.• Carboxylic acids will have O-H also.• Aldehydes have two C-H signals around
2700 and 2800 cm-1. =>
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IR spectroscopyA Ketone IR Spectrum
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IR spectroscopyAn Aldehyde IR Spectrum
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IR spectroscopyO-H Stretch of a Carboxylic Acid
This O-H absorbs broadly, 2500-3500 cm-1, due to strong hydrogen bonding.
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IR spectroscopyVariations in C=O Absorption
• Conjugation of C=O with C=C lowers the stretching frequency to ~1680 cm-1.
• The C=O group of an amide absorbs at an even lower frequency, 1640-1680 cm-1.
• The C=O of an ester absorbs at a higher frequency, ~1730-1740 cm-1.
• Carbonyl groups in small rings (5 C’s or less) absorb at an even higher frequency. =>
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IR spectroscopyAn Amide IR Spectrum
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IR spectroscopyCarbon - Nitrogen Stretching
• C - N absorbs around 1200 cm-1.• C = N absorbs around 1660 cm-1 and is
much stronger than the C = C absorption in the same region.
• C ≡ N absorbs strongly just above 2200 cm-1. The alkyne C ≡ C signal is much weaker and is just below 2200 cm-1 .
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IR spectroscopyA NitrileIR Spectrum
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IR spectroscopySummary of IR
Absorptions
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IR spectroscopyStrengths and Limitations
• IR alone cannot determine a structure.• Some signals may be ambiguous.• The functional group is usually indicated.• The absence of a signal is definite proof
that the functional group is absent.• Correspondence with a known sample’s
IR spectrum confirms the identity of the compound. =>