Spectroscopie infrarouge
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概述
Source : Vy M. Dong et Zhiwei Chen, Department of Chemistry, University of California, Irvine, CA
Cette expérience démontrera l’utilisation de la spectroscopie infrarouge (IR) (également connu sous le nom la spectroscopie vibrationnelle) afin d’élucider l’identité d’un composé inconnu en identifiant le cycle actuel. Spectres IR seront obtenus sur un spectromètre IR à l’aide de la réflexion totale atténuée technique d’échantillonnage (RTA) auprès d’un échantillon pur de l’inconnu.
Principles
Une liaison covalente entre deux atomes peut être considérée comme deux objets avec masses m1 et m2 qui sont reliés avec un ressort. Naturellement, cette obligation s’étend et compresse avec une certaine fréquence vibratoire. Cette fréquence 
est donnée par l’équation 1, où k est la constante de force du ressort, c est la vitesse de la lumière et µ est la masse réduite (équation 2). La fréquence est généralement mesurée en nombres d’ondes, qui sont exprimées en centimètres inverses (cm-1).
De l’équation 1, la fréquence est proportionnelle à la force du ressort et inversement proportionnelle à la masse des objets. Ainsi, C-H, N-H et les liaisons O-H ont plus élevé qui s’étend de fréquences que C-C et les liaisons C-O, comme l’hydrogène est un atome de lumière. Doubles et triples liaisons peut être considérés comme des ressorts plus forts, donc une double liaison C-O a une fréquence plus élevée qui s’étend à une liaison simple de C-O. La lumière infrarouge est un rayonnement électromagnétique avec des longueurs d’onde allant de 700 nm et 1 mm, ce qui concorde avec les forces de liaison relatif. Quand une molécule absorbe la lumière infrarouge avec une fréquence égale à la fréquence de vibration naturelle d’une liaison covalente, l’énergie du rayonnement produit une augmentation de l’amplitude de la vibration de la liaison. Si l’électronégativité (tendance à attirer les électrons) des deux atomes dans une liaison covalente sont très différents, une séparation de charge se produit qui se traduit par un moment dipolaire. Par exemple, dans une double liaison C-O (un groupe carbonyle), les électrons passent plus de temps autour de l’atome d’oxygène que l’atome de carbone, l’oxygène étant plus électronégatif que le carbone. Par conséquent, il y a un moment dipolaire net, ce qui entraîne une charge partielle négative sur l’oxygène et une charge partielle positive sur le carbone. En revanche, un alcyne symétrique n’a pas un moment dipolaire net parce que les deux moments dipolaires individuels de chaque côté s’annulent mutuellement. L’intensité de l’absorption infrarouge est proportionnelle à la variation du moment dipolaire lorsque le cautionnement s’étend ou compresse. Par conséquent, un tronçon de groupement carbonyle montrera une bande intense dans l’IR et un alcyne interne symétrique montrera un petit, si pas invisible, bande d’élongation de la liaison triple C-C (Figure 1). Le tableau 1 montre certaines fréquences d’absorption caractéristique. La figure 2 montre le spectre infrarouge d’un ester de Hantzsch. Remarquez le pic à 3 343 cm-1 pour la liaison simple N-H et un pic à 1 695 cm-1 pour les groupes carbonyles. Dans cette expérience, la technique d’échantillonnage de RTA est utilisée, où la lumière infrarouge réfléchit l’échantillon qui est en contact avec un cristal de RTA plusieurs fois. En général, les matériaux avec un indice de réfraction élevé sont utilisés, comme le séléniure de zinc et de germanium. Cette méthode permet d’examiner directement les analytes solide ou liquide, sans plus de préparation.
Figure 1. Schéma montrant la C–O double et C–C triple liaison étendues et le changement de moment dipolaire résultant.
Le tableau 1. Fréquences de IR caractéristiques des liaisons covalentes présents dans les molécules organiques.
La figure 2. Spectre infrarouge d’un ester de Hantzsch.
Procedure
Results
Table 2: Appearance and observed IR frequencies of the compounds listed in Figure 3.
| Compound Number | 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 |
| Appearance | clear liquid | white solid | clear liquid | clear liquid | clear liquid | clear liquid | yellow liquid | white solid | white solid | clear liquid |
| Observed frequencies (cm-1) | 1691, 1601, 1450, 1368, 1266 |
2773, 2730, 1713, 1591, 1576 |
2940, 2867, 1717, 1422, 1347 |
3026, 2948, 2920, 1605, 1496 |
2928, 2853, 1450, 904, 852 |
3926, 3315, 2959, 2120, 1461 |
3623, 3429, 3354, 2904, 1601 |
3408, 3384, 3087, 1596, 1496 |
3226, 2966, 1598, 1474, 1238 |
3340, 2959, 2861, 1468, 1460 |
Applications and Summary
In this experiment, we have demonstrated how to identify an unknown sample based on its characteristic IR spectrum. Different functional groups give different stretching frequencies, which allow the identification of the functional groups present.
As shown in this experiment, IR spectroscopy is a useful tool for the organic chemist to identify and characterize a molecule. In addition to organic chemistry, IR spectroscopy has useful applications in other areas. In the pharmaceutical industry, this technique is used for quantitative and qualitative analysis of drugs. In food science, IR spectroscopy is used to study fats and oils. Lastly, IR spectroscopy is used to measure the composition of greenhouse gases, i.e., CO2, CO, CH4, and N2O in efforts to understand global climate changes.
成績單
Infrared, or IR, spectroscopy is a technique used to characterize covalent bonds.
Molecules with certain types of covalent bonds can absorb IR radiation, causing the bonds to vibrate. An IR spectrophotometer can measure which frequencies are absorbed. This is generally represented with a spectrum of percent IR radiation transmitted through the sample at a given frequency in wavenumbers. In this type of spectrum, the peaks are inverted, as they represent a decrease in transmitted light at that frequency.
The absorbed frequencies depend on the identity and electronic environment of the bonds, giving each molecule a characteristic spectrum. However, each type of bond will absorb IR radiation within a specific frequency range, and will have a common peak shape and absorption strength. Peaks can therefore be assigned to specific bonds, allowing identification of an unknown compound from the IR spectrum.
This video will illustrate the characterization of an unknown organic compound with IR spectroscopy and will introduce a few other applications of IR spectroscopy in organic chemistry.
A covalent bond between two atoms can be modeled as a spring connecting two bodies with masses m1 and m2. This “spring” has a resonance frequency, which, in this case, is the frequency of light corresponding to the quantum of energy needed to excite an oscillation in the bond at that same frequency, but with even greater amplitude.
The resonance frequency of a bond depends on the bond strength and length, the identity of the involved atoms, and the environment. For instance, a conjugated bond will vibrate in a different frequency range than a non-conjugated bond.
The resonance frequency also depends on the vibrational mode, which is the oscillation pattern of the atoms within a molecule. The most common vibrational modes observed by IR spectroscopy are stretching and bending. Linear molecules have 3N minus 5 vibrational modes, where N is the number of atoms, and non-linear molecules have 3N minus 6 vibrational modes.
IR spectrophotometry is primarily performed by shining a broad-spectrum light source through an interferometer, which blocks all but a few wavelengths of light at any given time, onto the sample. An IR detector measures the light intensities for each interferometer setting. Once data has been collected over the desired frequency range, it is processed into a recognizable spectrum by Fourier transform.
The sample can be gaseous, liquid, or solid, depending on the construction of the instrument. For a standard detector, gases and liquids are placed in a cell with IR-transparent windows, and solids are suspended in oil or pressed into a transparent pellet with potassium bromide. The IR light is then directed through the sample to the detector.
An alternate method for solid and liquid samples is attenuated total reflectance, or ATR. In this method, the pure sample is placed in contact with a crystal surface. IR light is then reflected off the underside of the crystal into a detector, with the absorbed frequencies reflecting more weakly. The sample doesn’t need to be processed first, as the light does not travel through it.
Now that you understand the principles of IR spectroscopy, let’s go through a procedure for identifying an unknown organic compound using the ATR sampling technique on an FTIR instrument.
To begin the characterization procedure, turn on the FTIR spectrometer and allow the lamp to warm up to operating temperature.
Ensure that the ATR crystal is clean. Then, with no sample in place, use the spectrometer software to record a background spectrum.
Next, obtain a solid sample of an unknown organic compound and note its appearance. Using a clean metal spatula, carefully place the sample on the crystal surface. Alternatively, for liquid samples, a pipette is used to transfer samples to crystal surface.
Carefully screw down the probe until it locks into place to fix the sample against the crystal surface.
Then, collect at least one IR spectrum of the unknown sample. After data collection has finished and the background has been subtracted, use the analysis tools in the software to identify the wavenumbers of the peaks.
When finished with the spectrometer, remove the sample and clean the probe with acetone. Save the spectra, close the software, and turn off the spectrometer.
In this experiment, the unknown sample may be one of ten organic compounds, each with five characteristic IR peaks. Based on the phase and visual appearance of the unknown, 8 of the possibilities may be eliminated.
The spectrum from the unknown compound shows a wide peak near the 3,300 wavenumber region, indicative of either an -OH or -NH stretching absorption. The peaks to right indicate the presence of carbon-carbon double bonds and carbon oxygen bonds. Of the two remaining compounds, only one has an -OH group so the compound is phenol.
IR spectrophotometry is a widely used characterization tool in biology and chemistry. Let’s look at a few examples.
In this procedure, FTIR spectroscopy performed with the ATR method was used to obtain IR absorbance images of tissue by introducing a microscopy component into the instrument. Each pixel in the image had a corresponding IR spectrum, allowing determination of the molecular composition of the tissue with excellent spatial resolution. The tissue image could also be displayed at different frequencies to visualize the distribution of molecule types throughout the tissue.
The molecular vibrations of peptide groups in a protein are affected by protein conformational changes. By monitoring a protein sample with step-scan FTIR, which has a temporal resolution on the order of tens of nanoseconds, protein dynamics can be monitored via the changes in their absorbance spectra. The data can be presented as individual spectra or as 3D plots of intensity, frequency, and time for peak identification and further analysis.
You’ve just watched JoVE’s introduction to IR spectroscopy. You should now be familiar with the underlying principles of IR spectroscopy, the procedure for IR spectroscopy of organic compounds, and a few examples of how IR spectroscopy is used in organic chemistry. Thanks for watching!