Analyst

The most common type of infrared spectroscopy is FTIR (Fourier transform infrared) analysis. All infrared spectroscopies work on the principle that some infrared (IR) radiation is absorbed when it passes through a sample. First and foremost, it does not destroy the sample. Second, it is much faster than older techniques. Third, it is significantly more sensitive and precise.

How does FTIR analysis work?

The FTIR instrument passes infrared radiation ranging from 10,000 to 100 cm-1 through a sample, with some absorbed and some passing through. The sample molecules convert the absorbed radiation into rotational and/or vibrational energy. The resulting signal at the detector appears as a spectrum, typically ranging from 4000 cm-1 to 400cm-1, representing the sample’s molecular fingerprint. Because each molecule or chemical structure produces a distinct spectral fingerprint, FTIR analysis is an excellent tool for chemical identification.

HOW TO INTERPRET FTIR SPECTRUM?

The absorbed bands in the spectrum are only marginally discrete and degenerative. The specific “peak” of energy at a given wavenumber can shift due to other chemical and matrix factors (as well as by the way the incident energy is introduced). As a result, we don’t simply have a “look up” table that tells us where a specific band of energy belongs. The spectrum must be interpreted as a whole system, requiring the most experienced analysts in all spectrographic techniques to accurately characterize the functionality presented.
Although FTIR analysis is typically used to identify materials, it can also be used to quantify specific functional groups when the chemistry is understood and standard reference materials are available. The absorbance intensity will be proportional to the amount of functionality present in the sample.

It is necessary to determine which groups and bonds correspond to which peaks when reading the spectrum. Here is a simple reference tables for the various groups.

Table 1
Frequency RangeAbsorption (cm -1 )AppearanceGroupCompound ClassComments
4000-3000 cm -1 3700-3584medium, sharpO-H stretchingalcoholfree
3550-3200strong, broadO-H stretchingalcoholintermolecular bonded
3500mediumN-H stretchingprimary amine
3400
3400-3300mediumN-H stretchingaliphatic primary amine
3330-3250
3350-3310mediumN-H stretchingsecondary amine
3300-2500strong, broadO-H stretchingcarboxylic acidusually centered on 3000 cm -1
3200-2700weak, broadO-H stretchingalcoholintramolecular bonded
3000-2800strong, broadN-H stretchingamine salt
3000-2500 cm -1
3000-2500 cm -1 3333-3267strong, sharpC-H stretchingalkyne
3100-3000mediumC-H stretchingalkene
3000-2840mediumC-H stretchingalkane
2830-2695mediumC-H stretchingaldehydedoublet
2600-2550weakS-H stretchingthiol
2400-2000 cm -1
2400-2000 cm -1 2349strongO=C=O stretchingcarbon dioxide
2275-2250strong, broadN=C=O stretchingisocyanate
2260-2222weakCΞN stretchingnitrile
2260-2190weakCΞC stretchingalkynedisubstituted
2175-2140strongS-CΞN stretchingthiocyanate
2160-2120strongN=N=N stretchingazide
2150 C=C=O stretchingketene
2145-2120strongN=C=N stretchingcarbodiimide
2140-2100weakCΞC stretchingalkynemonosubstituted
2140-1990strongN=C=S stretchingisothiocyanate
2000-1900mediumC=C=C stretchingallene
2000 C=C=N stretchingketenimine
2000-1650 cm -1
2000-1650 cm -1 2000-1650weakC-H bendingaromatic compoundovertone
1870-1540
1818strongC=O stretchinganhydride
1750
1815-1785strongC=O stretchingacid halide
1800-1770strongC=O stretchingconjugated acid halide
1775strongC=O stretchingconjugated anhydride
1720
1770-1780strongC=O stretchingvinyl / phenyl ester
1760strongC=O stretchingcarboxylic acidmonomer
1750-1735strongC=O stretchingesters6-membered lactone
1750-1735strongC=O stretchingδ-lactoneγ: 1770
1745strongC=O stretchingcyclopentanone
1740-1720strongC=O stretchingaldehyde
1730-1715strongC=O stretchingα,β-unsaturated esteror formates
1725-1705strongC=O stretchingaliphatic ketoneor cyclohexanone or cyclopentenone
1720-1706strongC=O stretchingcarboxylic aciddimer
1710-1680strongC=O stretchingconjugated aciddimer
1710-1685strongC=O stretchingconjugated aldehyde
1690strongC=O stretchingprimary amidefree (associated: 1650)
1690-1640mediumC=N stretchingimine / oxime
1685-1666strongC=O stretchingconjugated ketone
1680strongC=O stretchingsecondary amidefree (associated: 1640)
1680strongC=O stretchingtertiary amidefree (associated: 1630)
1650strongC=O stretchingδ-lactamγ: 1750-1700 β: 1760-1730
1670-1600 cm -1
1670-1600 cm -1 1678-1668weakC=C stretchingalkenedisubstituted (trans)
1675-1665weakC=C stretchingalkenetrisubstituted
1675-1665weakC=C stretchingalkenetetrasubstituted
1662-1626mediumC=C stretchingalkenedisubstituted (cis)
1658-1648mediumC=C stretchingalkenevinylidene
1650-1600mediumC=C stretchingconjugated alkene
1650-1580mediumN-H bendingamine
1650-1566mediumC=C stretchingcyclic alkene
1648-1638strongC=C stretchingalkenemonosubstituted
1620-1610strongC=C stretchingα,β-unsaturated ketone
1600-1300 cm -1
1600-1300 cm -1 1550-1500strongN-O stretchingnitro compound
1372-1290
1465mediumC-H bendingalkanemethylene group
1450mediumC-H bendingalkanemethyl group
1375
1390-1380mediumC-H bendingaldehyde
1385-1380mediumC-H bendingalkanegem dimethyl
1370-1365
1400-1000 cm -1
1400-1000 cm -1 1440-1395mediumO-H bendingcarboxylic acid
1420-1330mediumO-H bendingalcohol
1415-1380strongS=O stretchingsulfate
1200-1185
1410-1380strongS=O stretchingsulfonyl chloride
1204-1177
1400-1000strongC-F stretchingfluoro compound
1390-1310mediumO-H bendingphenol
1372-1335strongS=O stretchingsulfonate
1195-1168
1370-1335strongS=O stretchingsulfonamide
1170-1155
1350-1342strongS=O stretchingsulfonic acidanhydrous
1165-1150 hydrate: 1230-1120
1350-1300strongS=O stretchingsulfone
1160-1120
1342-1266strongC-N stretchingaromatic amine
1310-1250strongC-O stretchingaromatic ester
1275-1200strongC-O stretchingalkyl aryl ether
1075-1020
1250-1020mediumC-N stretchingamine
1225-1200strongC-O stretchingvinyl ether
1075-1020
1210-1163strongC-O stretchingester
1205-1124strongC-O stretchingtertiary alcohol
1150-1085strongC-O stretchingaliphatic ether
1124-1087strongC-O stretchingsecondary alcohol
1085-1050strongC-O stretchingprimary alcohol
1070-1030strongS=O stretchingsulfoxide
1050-1040strong, broadCO-O-CO stretchinganhydride
1000-650 cm -1
1000-650 cm -1 995-985strongC=C bendingalkenemonosubstituted
915-905
980-960strongC=C bendingalkenedisubstituted (trans)
895-885strongC=C bendingalkenevinylidene
850-550strongC-Cl stretchinghalo compound
840-790mediumC=C bendingalkenetrisubstituted
730-665strongC=C bendingalkenedisubstituted (cis)
690-515strongC-Br stretchinghalo compound
600-500strongC-I stretchinghalo compound
900-700 cm -1
900-700 cm -1 880 ± 20strongC-H bending1,2,4-trisubstituted
810 ± 20
880 ± 20strongC-H bending1,3-disubstituted
780 ± 20
(700 ± 20)
810 ± 20strongC-H bending1,4-disubstituted or
1,2,3,4-tetrasubstituted
780 ± 20strongC-H bending1,2,3-trisubstituted
(700 ± 20)
755 ± 20strongC-H bending1,2-disubstituted
750 ± 20strongC-H bendingmonosubstituted
700 ± 20 benzene derivative

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Table 2.

Compound ClassGroupAbsorption (cm -1 )AppearanceComments
acid halideC=O stretching1815-1785strong
alcoholsO-H stretching3700-3584medium, sharpfree
O-H stretching3550-3200strong, broadintermolecular bonded
O-H stretching3200-2700weak, broadintramolecular bonded
O-H bending1420-1330medium
aldehydeC-H stretching2830-2695mediumdoublet
C=O stretching1740-1720strong
C-H bending1390-1380medium
aliphatic etherC-O stretching1150-1085strong
aliphatic ketoneC=O stretching1725-1705strongor cyclohexanone or cyclopentenone
aliphatic primary amineN-H stretching3400-3300medium
alkaneC-H stretching3000-2840medium
C-H bending1465mediummethylene group
C-H bending1450mediummethyl group
C-H bending1385-1380mediumgem dimethyl
C-H stretching3100-3000medium
C=C stretching1678-1668weakdisubstituted (trans)
C=C stretching1675-1665weaktrisubstituted
C=C stretching1675-1665weaktetrasubstituted
C=C stretching1662-1626mediumdisubstituted (cis)
C=C stretching1658-1648mediumvinylidene
C=C stretching1648-1638strongmonosubstituted
C=C bending995-985strongmonosubstituted
C=C bending980-960strongdisubstituted (trans)
C=C bending895-885strongvinylidene
C=C bending840-790mediumtrisubstituted
C=C bending730-665strongdisubstituted (cis)
alkyl aryl etherC-O stretching1275-1200strong
alkyneC-H stretching3333-3267strong, sharp
CΞC stretching2260-2190weakdisubstituted
CΞC stretching2140-2100weakmonosubstituted
alleneC=C=C stretching2000-1900medium
amineN-H bending1650-1580medium
C-N stretching1250-1020medium
amine saltN-H stretching3000-2800strong, broad
anhydrideC=O stretching1818strong
CO-O-CO stretching1050-1040strong, broad
aromatic amineC-N stretching1342-1266strong
aromatic compoundC-H bending2000-1650weakovertone
aromatic esterC-O stretching1310-1250strong
azideN=N=N stretching2160-2120strong
benzene derivative 700 ± 20
carbodiimideN=C=N stretching2145-2120strong
carbon dioxideO=C=O stretching2349strong
carboxylic acidO-H stretching3300-2500strong, broadusually centered on 3000 cm -1
C=O stretching1760strongmonomer
C=O stretching1720-1706strongdimer
O-H bending1440-1395medium
conjugated acidC=O stretching1710-1680strongdimer
conjugated acid halideC=O stretching1800-1770strong
conjugated aldehydeC=O stretching1710-1685strong
conjugated alkeneC=C stretching1650-1600medium
conjugated anhydrideC=O stretching1775strong
conjugated ketoneC=O stretching1685-1666strong
cyclic alkeneC=C stretching1650-1566medium
cyclopentanoneC=O stretching1745strong
esterC-O stretching1210-1163strong
estersC=O stretching1750-1735strong6-membered lactone
fluoro compoundC-F stretching1400-1000strong
halo compoundC-Cl stretching850-550strong
C-Br stretching690-515strong
C-I stretching600-500strong
imine / oximeC=N stretching1690-1640medium
isocyanateN=C=O stretching2275-2250strong, broad
isothiocyanateN=C=S stretching2140-1990strong
keteneC=C=O stretching2150
ketenimineC=C=N stretching2000
monosubstitutedC-H bending750 ± 20strong
nitrileCΞN stretching2260-2222weak
nitro compoundN-O stretching1550-1500strong
none 3330-3250
none 1870-1540
none 1750
none 1720
none 1372-1290
none 1375
none 1370-1365
none 1200-1185
none 1204-1177
none 1195-1168
none 1170-1155
none 1165-1150 hydrate: 1230-1120
none 1160-1120
none 1075-1020
none 1075-1020
none 915-905
none 810 ± 20
none 780 ± 20
none (700 ± 20)
none (700 ± 20)
phenolO-H bending1390-1310medium
primary alcoholC-O stretching1085-1050strong
primary amideC=O stretching1690strongfree (associated: 1650)
N-H stretching3500medium
secondary alcoholC-O stretching1124-1087strong
secondary amideC=O stretching1680strongfree (associated: 1640)
secondary amineN-H stretching3350-3310medium
sulfateS=O stretching1415-1380strong
sulfonamideS=O stretching1370-1335strong
sulfonateS=O stretching1372-1335strong
sulfoneS=O stretching1350-1300strong
sulfonic acidS=O stretching1350-1342stronganhydrous
sulfonyl chlorideS=O stretching1410-1380strong
sulfoxideS=O stretching1070-1030strong
tertiary alcoholC-O stretching1205-1124strong
tertiary amideC=O stretching1680strongfree (associated: 1630)
thiocyanateS-CΞN stretching2175-2140strong
thiolS-H stretching2600-2550weak
vinyl / phenyl esterC=O stretching1770-1780strong
vinyl etherC-O stretching1225-1200strong
α,β-unsaturated esterC=O stretching1730-1715strongor formates
α,β-unsaturated ketoneC=C stretching1620-1610strong
δ-lactamC=O stretching1650strongγ: 1750-1700 β: 1760-1730
δ-lactoneC=O stretching1750-1735strongγ: 1770
1,2,3,4-tetrasubstituted
1,2,3-trisubstitutedC-H bending780 ± 20strong
C-H bending880 ± 20strong
1,2-disubstitutedC-H bending755 ± 20strong
C-H bending880 ± 20strong
1,4-disubstituted orC-H bending810 ± 20strong

What does FTIR serve as a tool for?

Unknown materials (e.g., films, solids, powders, or liquids) and contamination on or in a material (e.g., particles, fibers, powders) can be identified and characterized by FTIR analysis.

FTIT sample preparation:

The ability to introduce and observe energy from a specific matrix is required for proper FTIR analysis. To properly analyse the sample, we have many sample preparation and introduction techniques available in the laboratory. Transmission was the only available method of analysis in the early days of infrared spectroscopy. For transmission analysis, the sample had to be made translucent to laser and infrared energy by directly inserting it into the optical path, casting a thin film on a salt crystal, or mixing a powder version of the sample with a salt and casting.
Today, however, we can use not only transmission techniques but also reflectance techniques. We generally rely on variations of ATR (Attenuated Total Reflectance) techniques to introduce and observe energy because we can focus and manipulate the incident beam with optics. ATR involves the use of an internal reflectance phenomenon to propagate incident energy.

The beam is introduced into a crystal at an incident angle, allowing internal reflectance “bounces” at the bottom and top of the crystal before leaving on the opposite side. The sample is brought into contact with the crystal at the top, causing energy interaction at the crystal and sample interface, which is where the bounce positions are located. The more bounce positions there are, the greater the energy transfer (and thus the better the spectral response), but single bounce systems are used when a very small area needs to be analyzed.
A HATR (Horizontal Attenuated Total Reflectance) will be typically used for liquid and paste samples, which will involve placing the sample on a crystal plate or trough in a horizontal position so that gravity acts to make intimate contact with the cell. The depth of penetration into the sample can be varied by using different crystals. For example, we will use a germanium crystal for rubber analysis to limit the effect of highly IR absorbing materials in rubber (specifically carbon black), but the zinc selenide crystal is the crystal of choice for durability, moisture resistance, and penetration depth in normal everyday samples.

What are Advantages and Disadvantages of FTIR analysis?

Advantages:

Disadvantages:

Different types of FTIR Analysis

Transmission FTIR: In this method, the sample is placed between two transparent windows, and the infrared light passes through the sample. The amount of light absorbed by the sample at each frequency is measured, and this data is used to construct a spectrum of the sample’s chemical composition. This method is useful for analyzing samples that are transparent to infrared radiation.

Attenuated Total Reflection (ATR) FTIR: In this method, the sample is placed in contact with a crystal surface, and the infrared light is absorbed by the sample at the surface. The amount of light absorbed by the sample at each frequency is measured, and this data is used to construct a spectrum of the sample’s chemical composition. This method is useful for analyzing samples that are not transparent to infrared radiation, such as liquids or solids.

Diffuse Reflectance FTIR: In this method, the sample is ground into a powder and placed on a reflective surface, and the infrared light is reflected off the sample. The amount of light absorbed by the sample at each frequency is measured, and this data is used to construct a spectrum of the sample’s chemical composition. This method is useful for analyzing samples that are difficult to prepare in a thin, transparent film, such as powders or rough surfaces.

Fourier Transform Raman Spectroscopy (FT-Raman): In this method, the sample is irradiated with a laser, and the scattered light is analyzed by a Fourier transform spectrometer. The frequency of the scattered light is shifted due to interactions with the sample’s chemical bonds, and this shift is used to construct a spectrum of the sample’s chemical composition. This method is useful for analyzing samples that are not easily analyzed by FTIR, such as inorganic materials or samples with strong fluorescence.

Infrared Microscopy: In this method, a microscope is used to focus the infrared beam on a small area of the sample, allowing for spatially resolved measurements. The amount of light absorbed by the sample at each frequency is measured, and this data is used to construct a spectrum of the sample’s chemical composition. This method is useful for analyzing samples that have spatially varying chemical composition, such as polymer blends or biological tissues.

strengths and limitations of fifferent types of FTIR

Each type of FTIR analysis has its own strengths and limitations, and the choice of which method to use depends on the specific sample and analysis requirements.

Transmission FTIR is a commonly used method and is suitable for analyzing samples that are transparent to infrared radiation. It is also a relatively simple and straightforward method, and the data can be easily compared to reference spectra in a library.

ATR-FTIR is useful for analyzing samples that are not transparent to infrared radiation, and it can be used with a wide range of sample types, including liquids, solids, and powders. ATR-FTIR is also relatively easy to use, and the data can be compared to reference spectra in a library.

Diffuse Reflectance FTIR is useful for analyzing samples that are difficult to prepare in a thin, transparent film, such as powders or rough surfaces. It is also a relatively simple method and can be used to analyze a wide range of sample types.

FT-Raman spectroscopy is useful for analyzing samples that are not easily analyzed by FTIR, such as inorganic materials or samples with strong fluorescence. It can also be used to provide complementary information to FTIR analysis.

Infrared microscopy is useful for analyzing samples that have spatially varying chemical composition, such as polymer blends or biological tissues. It provides spatially resolved measurements and can be used to analyze small or complex samples.

In summary, the choice of which type of FTIR analysis to use depends on the specific sample and analysis requirements. Each method has its own advantages and limitations, and the most suitable method should be selected based on the nature of the sample and the analysis needs.