FT-IR Spectroscopy. An introduction in measurement techniques and interpretation

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FT-IR Spectroscopy An introduction in measurement techniques and interpretation

History Albert Abraham Michelson (1852-1931) Devised Michelson Interferometer with Edward Morley in 1880 (Michelson-Morley experiment) Detects the motion of the earth through the ether There was no! Death knell for the ether theory No detector was available Nonexistence of Fourier Transform algorithms capable of being performed by human calculators Rubens and Wood presented the first real interferogram in 1911

History 1950-1960 Air Force Cambridge Research Laboratories at John Hopkins University tested high resolution spectrometers for astronomical applications Cooley and Tukey algorithm allowed computing of Fourier transforms in 1965 The critical factorization step used by Cooley an Tukey had already been recognized and described by Gauss as early as 1805!

What is FT-IR? Fourier Transform InfraRed Spectroscopy Advancement of dispersive spectrometers Interferometer Beamsplitter Interferogram After recording Fourier Transformation Mathematical technique

Interferometer Michelson Interferometer Beamsplitter splits up light Reflected on moveable and fixed mirror Interference after recombination By smoothly translating the movable mirror, the optical path difference between the beams reflecting off the two mirrors is varied continuously which leads to a change of wavelength Interferogram

Interferogram Sum of cosine signals of all frequencies Translation of the symmetric interferogram into a spectrum by Fourier Transformation: I S ( ~ ν ) = ( x)cos(2π ~ νx) dx

Interferogram Experimental interferograms are asymmetric due to phase shifts Complex FT required, including cosine and sine terms

Dispersive vs. FT-spectroscopy FT-devices have multiple advantages compared to dispersive devices: Multiplex-Advantage: Capability of a complete wavelength scan at a time Reduced background noise Less scan time Throughput-Advantage: Optical throughput is ten times higher Connes-Advantage: Stable wavenumber because of internal reference (He-Ne-Laser)

Interpretation Typical absorbance positions: Lipids =CH 2 : 3100-3000 -CH 2 -, -CH 3 : 3000-2850 Protein Amide I: 1690-1600 Water Lipids Amide I Amide II DNA/RNA Protein Amide II: 1575-1480 Nucleic Acid: -PO 2- : 1225; 1084

Amide I & Amide II Amide I: -C=O (stretch) prim. Amids sec. Amids tert. Amids Amide II: -C-N (stretch); -C-N-H (deformation) prim. Amids sec. Amids Secondary structure of proteins (α-helix, ß-sheet, random coil)

Amide I Here an example for varying secondary structure: random coil alpha helix ß-sheet

Sample Recording Solid samples are recorded with KBr pressed as a pellet Liquid samples are recorded with water as solvent Adjuvants have to be subtracted after recording to obtain the pure protein spectrum The spectrum is recorded with wavelength [cm -1 ] on the abscissa and transmission [T%] or absorbance [A] on the ordinate

Interpretation

First steps Truncate the spectrum to the favored Amide region (Amide I: 1720-1580cm -1 ) Baseline correction Fits a straight baseline to the non peak sections of a trace

Baseline correction

First steps Fourier Self-Deconvolution High pass Fast Fourier Transform filter Based on a method described by Griffiths and Pariente in 1986 Two filters Exponential filter is used to sharpen spectral features γequals the FWHH of the widest resolvable peak Smoothing filter FSD tends to increase the noise in the data Bessel filter is applied

Fourier Self Deconvolution

Qualitative Interpretation The 2nd derivative Convolution technique described 1964 by Savitzky and Golay Reveals the secondary structure of the protein sample

Quantitative Interpretation Quantitative interpretation is a quite difficult technique Operator dependent method Starting with the deconvoluted trace a peak fitting is performed Algorithm is described by Marquardt and known as the Levenberg-Marquardt method in 1963 There are multiple solutions for one trace Even though the algorithm appears to have found a minimum, there may be a better solution for a given number of peaks and line shapes Operater has to give more information

Example

Same, same but different

And then? The peak report contains Number of peaks Peak positions Area of the peak (AUC) The sum of the AUCs represents the amount of secondary structure if related to the 2nd derivative peak positions