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multiple broad peaks C─O alcohols: primary 1040–1060 strong, broad secondary ~1100 strong tertiary 1150–1200 medium phenols any 1200 ethers aliphatic 1120 aromatic 1220–1260 carboxylic acids any 1250–1300 esters any 1100–1300 two bands (distinct from ketones, which do not possess a C─O bond) C─N aliphatic amines any 1020–1220
Fourier transform infrared spectroscopy (FTIR) [1] is a technique used to obtain an infrared spectrum of absorption or emission of a solid, liquid, or gas. An FTIR spectrometer simultaneously collects high-resolution spectral data over a wide spectral range.
The intrinsic physicochemical property of each particular molecule determines its corresponding IR absorbance peak, and therefore can provide characteristic fingerprints of functional groups (e.g. C-H, O-H, C=O, etc.). [1] In geosciences research, FTIR is applied extensively in the following applications:
The peak at the center is the ZPD position ("zero path difference"): Here, all the light passes through the interferometer because its two arms have equal length. The method of Fourier-transform spectroscopy can also be used for absorption spectroscopy. The primary example is "FTIR Spectroscopy", a common technique in chemistry.
The dispersive method is more common in UV-Vis spectroscopy, but is less practical in the infrared than the FTIR method. One reason that FTIR is favored is called "Fellgett's advantage" or the "multiplex advantage": The information at all frequencies is collected simultaneously, improving both speed and signal-to-noise ratio.
A common spectroscopic method for analysis is Fourier transform infrared spectroscopy (FTIR), where chemical bonds can be detected through their characteristic infrared absorption frequencies or wavelengths. These absorption characteristics make infrared analyzers an invaluable tool in geoscience, environmental science, and atmospheric science.
The linear absorption (FTIR) spectrum is indicated above the 2D IR spectrum. The two peaks in the 1D spectrum reveal no information on coupling between the two states. After the waiting time in the experiment, it is possible to reach double excited states. This results in the appearance of an overtone peak.
ATR-FTIR is also used as a tool in pharmacological research to investigate protein/pharmaceutical interactions in detail. Water-soluble proteins to be investigated require Polyhistidine-tags , allowing the macromolecule to be anchored to a lipid bilayer, which is attached to a Germanium crystal or other suitable optical media.