VIBRATIONAL
SPECTROSCOPY

FROM THEORY
TO PRACTICE

edited by
Kamilla Malek

Cover and title page design:
Marek Goebel

Project editor:
Katarzyna Włodarczyk-Gil

Editorial coordinator:
Iwona Lewandowska

Copy editor:
Łukasz Boda

Production coordinator:
Mariola Grzywacka

Edited by:
Kamilla Malek, Faculty of Chemistry, Jagiellonian University

The publication was co-funded by the Faculty of Chemistry of the Jagiellonian University in Krakow

The book that you have purchased is the work of its author and publisher. Please respect their rights. You may make this book available free of charge to your family and friends, but do not publish it on the net. If you quote excerpts from it, do not change the original and always be sure to mention where they come from. And if you copy parts of it, do so only for your own use.
It is imperative that we respect other people’s rights and property.
See more on www.legalnakultura.pl

Polska Izba Książki

Copyright © by Wydawnictwo Naukowe PWN SA
Warszawa 2016

This book has been prepared based on paper editon from 2016 (First edition)

Warszawa 2016

ISBN 978-83-01-18893-1

Wydawnictwo Naukowe PWN SA

02-460 Warszawa, ul. Gottlieba Daimlera 2

tel. 22 69 54 321, faks 22 69 54 288

infolinia 801 33 33 88

e-mail: pwn@pwn.com.pl

www.pwn.pl

The typesetting of the electronic version commissioned by WN PWN: Mobisfera/Karol Ossowski

Vibrational spectroscopy. From theory to practice
Editor Kamilla Malek

AUTHORS

Barańska Małgorzata, Prof., PhD, DSc
Faculty of Chemistry, Jagiellonian University in Krakow

Bukowska Jolanta, Prof., PhD, DSc
Faculty of Chemistry, University of Warsaw

Chmura-Skirlińska Antonina, PhD
Jagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University in Krakow

Chruszcz-Lipska Katarzyna, PhD
AGH University of Science and Technology, Faculty of Drilling, Oil and Gas

Czamara Krzysztof, MSc
Faculty of Chemistry, Jagiellonian University in Krakow

Dybaś Jakub, MSc
Faculty of Chemistry, Jagiellonian University in Krakow

Gąsior-Głogowska Marlena, PhD, Eng.
Faculty of Fundamental Problems of Technology, Wroclaw University of Science and Technology

Jaworska Aleksandra, PhD
Faculty of Chemistry, Jagiellonian University in Krakow

Kaczor Agnieszka, PhD, DSc
Faculty of Chemistry, Jagiellonian University in Krakow

Kochan Kamila, MSc
Faculty of Chemistry, Jagiellonian University in Krakow

Królikowska Agata, PhD
Faculty of Chemistry, University of Warsaw

Lipiński Piotr, F.J., PhD
Mossakowski Medical Research Centre, Polish Academy of Sciences

Majzner Katarzyna, PhD
Faculty of Chemistry, Jagiellonian University in Krakow

Malek Kamilla, PhD, DSc
Faculty of Chemistry, Jagiellonian University in Krakow

Marzec Katarzyna M., PhD
Jagiellonian Centre for Experimental Therapeutics (JCET), Jagiellonian University in Krakow

Miśkowiec Paweł, PhD
Faculty of Chemistry, Jagiellonian University in Krakow

Oleszko Adam, MSc, Eng.
Faculty of Fundamental Problems of Technology, Wroclaw University of Science and Technology

Pacia Marta Z., MSc
Faculty of Chemistry, Jagiellonian University in Krakow

Rode Joanna, PhD
1. Institute of Nuclear Chemistry and Technology 2. Institute of Organic Chemistry, Polish Academy of Sciences

Ryguła Anna, PhD
Jagiellonian Centre for Experimental Therapeutics (JCET), Faculty of Chemistry, Jagiellonian University in Krakow

Staniszewska-Ślęzak Emilia, MSc
Faculty of Chemistry, Jagiellonian University in Krakow

Wiercigroch Ewelina, MSc
Faculty of Chemistry, Jagiellonian University in Krakow

Wróbel Tomasz, PhD
Faculty of Chemistry, Jagiellonian University in Krakow

Zając Grzegorz, MSc
Faculty of Chemistry, Jagiellonian University in Krakow

mContent

Cover

Title page

Editorial page

Content

1. Fundamentals of infrared spectroscopy (FT-IR)
(Kamilla Malek, Emilia Staniszewska-Ślęzak, Kamila Kochan, Katarzyna Majzner)

1.1. Quantum description – models of the harmonic and anharmonic oscillators

1.2. Normal coordinates

1.3. Construction of a FT-IR spectrometer

1.3.1. Light source

1.3.2. Interferometer

1.3.3. Sample chamber

1.3.4. Detector

2. Fundamentals of Raman scattering spectroscopy
(Kamilla Malek, Małgorzata Barańska, Kamila Kochan)

2.1. Quantum description of Raman scattering

2.2. Instrumentation in Raman spectroscopy

2.2.1. Laser

2.2.2. Sample compartment

2.2.3. Optical element splitting the beam of electromagnetic radiation

2.2.4. Detector

3. Special FT-IR techniques

3.1. Sampling techniques in FT-IR spectroscopy (Paweł Miśkowiec)

3.1.1. Transmission technique

3.1.2. Reflexive techniques

3.1.2.1. Attenuated total reflection, ATR

3.1.2.2. Diffuse reflection in the mid-infrared range, DRIFT

3.1.2.3. Reflection – absorption infrared spectroscopy, IRRAS

3.1.3. Photoacoustic spectroscopy, PAS

3.1.4. Infrared emission spectroscopy, ES (IRES)

3.2. FT-IR microscopy and imaging (Ewelina Wiercigroch, Kamilla Malek )

3.3. Vibrational circular dichroism (Piotr F. J. Lipiński)

3.3.1. Chirality

3.3.2. What is Vibrational Circular Dichroism?

3.3.3. How is VCD measured?

3.3.4. Applications of VCD spectroscopy

3.3.5. Calculations of VCD spectra and their problems

3.3.5. Very short summary of current developments

4. Special Raman techniques

4.1. Resonance Raman scattering spectroscopy (Katarzyna M. Marzec, Jakub Dybaś)

4.1.1. Resonance versus normal Raman scattering and fluorescence

4.1.2. Phenomenon of Resonance Raman scattering

4.1.3. Application and potential of RRS

4.1.4. Instrumentation

4.2. Surface-enhanced Raman scattering spectroscopy (SERS) (Agata Królikowska, Jolanta Bukowska)

4.2.1. Mechanism of surface enhancement

4.2.2. Types of the substrates used in SERS spectroscopy

4.2.3. SERS spectral features

4.2.4. Applications of SERS spectroscopy

4.3. Raman Optical Activity (ROA) (Joanna E. Rode)

4.3.1. Schematic diagram of ROA phenomenon

4.3.2. Theoretical description of ROA phenomenon

4.3.3. Instrumentation

4.3.4. Applications of ROA

4.3.5. Summary

4.4. Raman imaging (Agnieszka Kaczor)

5. Chemometric analysis of FT-IR and Raman spectra
(Katarzyna Majzner, Kamila Kochan, Małgorzata Barańska)

5.1. Analysis of marker bands

5.2. Cluster analysis (CA)

5.2.1. Hierarchical cluster analysis (HCA)

5.2.2. Non-hierarchical cluster analysis

5.2.3. Comparison of HCA, KMCA and FCA methods

6. Selected applications of FT-IR spectroscopy

6.1. An effect of molecular symmetry and isotopic substitution on IR and Raman spectra of chloromethane derivatives (Kamilla Malek, Katarzyna M. Marzec)

6.2. Peak-fitting process by an example of ATR FT-IRspectra of soft tissues (Marlena Gąsior-Głogowska, Adam Oleszko)

6.2.1. Skin

6.2.2. Skin’s proteins

6.2.3. Infrared spectroscopy of tissues

6.3. Synthesis and spectral characteristics of hydroxyapatites (Marlena Gąsior-Głogowska, Adam Oleszko)

6.3.1. Hydroxyapatites

6.3.2. Infrared spectroscopy of hydroxyapatite

6.4. The application of infrared spectroscopy for the determination of petroleum hydrocarbons in surface water and wastewater (Paweł Miśkowiec)

6.4.1. The composition of crude oil; environment pollution with petroleum products

6.4.2. The toxic properties of the components of crude oil

6.4.3. Legislation concerning problems of environmental pollution with petroleum products and methods of its measurement

6.4.4. An application of IR spectroscopy in analytical chemistry

6.4.5. Nernst distribution law

6.5. Determination of absolute configuration using vibrational circular dichroism (Piotr F. J. Lipiński)

6.5.1. Determination of absolute configuration via VCD

6.6. The identification of painting materials and degradation products. FT-IR imaging of paint layers (Emilia Staniszewska-Ślęzak, Kamilla Malek)

6.6.1. Chemical characteristics of a paint layer and products of its degradation

6.6.2. FT-IR spectroscopy as a technique used in the identification of chemical composition of artworks

6.7. Structural analysis of proteins by means of ft-ir spectroscopy (Katarzyna Majzner)

6.7.1. Anatomy of proteins

6.7.2. Application of FT-IR spectroscopy to studying proteins

6.8. Structural analysis of lipids by using infrared spectroscopy (Tomasz P. Wróbel)

6.8.1. Characteristics and occurrence of lipids

6.8.2. Application of FT-IR spectroscopy to studying lipids

6.9. Structural analysis of carbohydrates by means of FT-IRspectroscopy (Kamilla Malek, Ewelina Wiercigroch)

6.9.1. Molecular structure of carbohydrates

6.9.2. Characteristic IR bands of carbohydrates

6.10. An analysis of ATR FT-IRspectra of animal tissues (Emilia Staniszewska-Ślęzak, Kamilla Malek)

6.10.1. Biochemical features of selected animal tissues

6.10.2. FT-IR spectra of animal tissues

6.11. Diagnostics of disease development by FT-IR imaging of tissue (Kamila Kochan, Małgorzata Barańska)

7. Selected applications of Raman spectroscopy

7.1. The identification of proteins secondary structure in Raman spectra (Anna Rygula)

7.1.1. Characteristics of protein in Raman spectrum

7.1.2. Marker bands of amino acid residues

7.1.3. Other techniques of Raman spectroscopy for the analysis of proteins

7.2. Raman analysis of fatty acids (Aleksandra Jaworska, Małgorzata Barańska)

7.2.1. Occurrence and characteristics of fatty acids

7.2.2. An application of Raman spectroscopy in an analysis of fatty acids

7.3. Raman spectroscopy as a method to analyze lipids in animal tissues and mixtures (Krzysztof Czamara, Agnieszka Kaczor)

7.3.1. Classification of lipids

7.3.2. Spectroscopic characteristics of lipids

7.4. Polymorphism of model triacylgliceroles (Marta Z. Pacia, Krzysztof Czamara, Agnieszka Kaczor)

7.4.1. Polymorphism of lipids

7.4.2. Spectroscopic characteristics of TAGs polymorphs

7.5. Identification of carotenoids in plants by means of Raman spectroscopy (Aleksandra Jaworska, Małgorzata Barańska)

7.5.1. Structure, functions and occurrence of carotenoids

7.5.2. Raman bands of carotenoids

7.6. Identification of terpenes in citrus oils by means of Raman spectroscopy (Aleksandra Jaworska, Małgorzata Barańska, Kamilla Malek)

7.6.1. Essential oils – occurrence and composition

7.6.2. Identification of essential oils by means of gas chromatography and Raman spectroscopy

7.6.3. Chemometric analysis of Raman spectra of essential oils

7.7. An analysis of pigments and painting materials in Raman spectra (Anna Rygula, Kamilla Malek)

7.7.1. Raman spectroscopy as an analytic technique in conservation of art works

7.7.2. Structure of painting layers

7.7.3. Methodology of a Raman analysis of works of arts

7.8. Detection and determination of glucose in pharmaceuticals and body fluids (Agnieszka Kaczor)

7.9. Resonance Raman scattering spectroscopy in hemoglobin structure studies (Jakub Dybaś, Antonina Chmura-Skirlińska, Katarzyna M. Marzec)

7.9.1. Structure and physiology of hemoglobin

7.9.2. Resonance Raman scattering spectroscopy in hemoglobin studies

7.9.3. UV-Vis Absorption Spectrophotometry in hemoglobin studies

7.10. Identification of enantiomers of bornyl acetate and α-pinene in essential oils from the Siberian fir needles (Katarzyna Chruszcz-Lipska)

7.10.1. Terpenes

7.10.2. Stereochemistry of terpenes

7.10.3. Enantiomeric contents of terpenes in essential oils

7.10.4. Raman optical activity spectra of terpenes

7.11. Determination of absolute configuration of α-pinene enantiomers by means of Raman optical activity and quantum chemical calculations (Grzegorz Zając, Małgorzata Barańska)

7.11.1. Theoretical calculations of ROA

7.12. Estimation of surface enhancement factor and adsorption studies of 3-amino-5-mercapto-1,2,4-triazole (AMT) on silver using surface-enhanced Raman scattering spectroscopy (SERS) (Agata Królikowska, Jolanta Bukowska)

7.12.1. Surface enhancement factor in SERS

7.12.1.1. Types of definition of enhancement factor

7.12.1.2. Enhancement factor for a given substrate (EF)

7.12.1.3. Analytical enhancement factor (AEF)

7.12.1.4. Single molecule enhancement factor (SMEF)

7.12.2. The most common sources of errors in the determined values of SERS enhancement factors

7.12.3. Structure and properties of 3-amino-5-mercapto-1,2,4-triazole (AMT)

7.12.4. SERS spectrum of 3-amino-5-mercapto-1,2,4-triazole (AMT) on silver substrate

7.13. Identification and studying of distribution of caffeine in drug samples in situ (Małgorzata Barańska, Agnieszka Kaczor, Kamilla Malek)

7.14. Characteristics of the cell organelles based on analysis of marker bands and cluster analysis (Katarzyna Majzner)

7.14.1. The assignment of the major Raman bands in the cell spectra

7.14.2. An analysis of cell Raman imaging results

7.15. In vitro and in vivo Raman imaging of unicellular carotenoid producers (Marta Z. Pacia, Agnieszka Kaczor)

7.15.1. Spectral characteristics of cells compartments

Footnotes

4

Special Raman techniques

4.1. Resonance Raman scattering spectroscopy

Katarzyna M. Marzec, Jakub Dybaś

4.1.1. Resonance versus normal Raman scattering and fluorescence

Similar to normal Raman scattering (NR) Resonance Raman Scattering (RRS) can also be described as the two single-photon process. However, the difference appears in the energy of the excitation line. In the case of NR, such energy allows for the transition of the photon to the virtual state, which is far below the first electronic state. When the energy of virtual state corresponds to the energy of electronic excited state of a specific chromophoric group(s) in a molecule, the resonant enhancement is observed (Fig. 4.1.1.). The second part of the process is the same as in the case of NR: emission of the photon with the same (Rayleigh), lower (Stokes) or higher energy (anti-Stokes). The presence of the additional electronic transition in the case of RRS causes the strong enhancement (by a factor of 10³-10⁶) of specific bands originating from the chromophore group in Raman spectrum [1].

Fig. 4.1.1. Comparison of a simple diatomic energy levels for the normal Raman, resonance Raman and fluorescence spectra

The pre-resonance effect, which corresponds to the situation when the exciting line is close enough to the electronic excited state and also leads to bands enhancement, could also be observed.

The difference between RRS and fluorescence can be seen on the level of excited electronic state. The lifetime of this excited state for RRS is around 10⁻¹⁴ s, while for fluorescence, it may vary between 10⁻⁸-10-5 s. Moreover, the fluorescence spectrum is observed when the excited state molecule decays via non-radiative transitions (vibrational relaxation) from the discrete vibrational level of the excited electronic state to the lowest vibrational level of the excited state (which is not observed in RRS). Subsequently, this process is followed by the emission of radiation. Weak NR signals may be overwhelmed by fluorescence signals, as fluorescence is characterized by a longer excited state lifetime. This situation is observed not only for fluorescent molecules excited with specific wavelengths (in the range of visible light), but also for many complex samples where the signal is coming from the components’ matrix [2]. As an example we can present the autofluorescence of elastic lamina fibers when radiated with a laser wavelength of 532nm, even though the main components of this aorta structure (elastin and collagen) are not fluorescent molecules at this wavelength [3].

To eliminate the fluorescence interference in Raman spectra, different procedures may be carried out, starting with the use of different laser wavelengths as an excitation source. To obtain the Raman spectrum of some fluorescent proteins, a laser may be used to irradiate samples for some time before Raman measurement in order to cause the photon-induced destruction of the chromophore. Such a phenomenon is known as photobleaching and was previously used to obtain Raman spectra of proteins or biological samples. Fluorescence effects may also be reduced with the use of confocal Raman systems. In such laser scanning confocal instruments samples are penetrated only in a specific plane (the signal is not collected from the whole volume of the sample), reducing the fluorescent signal from potential contaminations. Secondly, in such conditions, the sample is excited to a high enough point to reach fluorophore saturation (molecules are in the excited state). As a consequence, an increase in the excitation wavelength produces an increase of Raman signal and a reduction in fluorescence emission.

4.1.2. Phenomenon of Resonance Raman scattering

As previously described in Chapter 2, the NR transition moment must have values different from zero (formula 2.3), which is determined by the change of polarizability during the transition between vibrational states, from initial m to final n (see Fig. 4.1.1.). Moreover, it was also postulated that the intensity of a normal Raman band is given by the equation 2.4, where νmn= νosc.

w22, (4.1)

In the case of RRS, αmn will represent the change of polarizability α during the transition between the m→e→n states, where e represents the electronic excited state (see Fig. 4.1.1.). That is why, the polarizability tensor αmn in RRS depends on the frequencies (νme and νen), as well as on the electric transition dipole moments (Mme and Men) which correspond to the energy differences between m→e→n states.

In NR, the sample is irradiated with an exciting line which energy is much smaller than that of electronic transition, so ν₀<<νme. Contrary to NR, in RRS, ν0 approaches νme, which also has an impact on the increase of the αmn value, and consequently on the significant increase of the intensity (Imn) of the Raman band at ν₀ – νmn. The intensity of resonance Raman scattering can be expected to be orders of magnitude greater than normal Raman scattering when ν0 approaches νme.

This shows that compared to non-resonant NR, even components at low concentrations may be detected and analysed with the use of the proper excitation wavelength, which proves the high sensitivity of this technique. Using RRS, it is possible to analyse samples even with nanomolar concentrations [4]. This also explains that to properly understand the observed RRS profile of a sample it is useful to know the UV-Vis absorption spectrum of the sample. To obtain RRS, a given sample is irradiated with an exciting line which coincides with the wavelength of an electronic transition of the sample. That is why the UV-Vis profile allows us to choose an exciting line which corresponds to the electronic transition of specific sample chromophore.

Fig. 4.1.2. The model of the UV-Vis absorption spectrum of molecule X containing two chromophoric groups A and B with two major absorption bands with the maxima at λA and λB. Exciting the Raman spectra at λA nm and λB nm results in two different resonantly enhanced Raman spectra of chromophore A and B, respectively. All parts of the molecule contribute to the non-resonant Raman spectrum excited at λC nm

Let’s take the theoretical molecule X, containing two chromophoric groups A  and B, which has an absorption spectrum with two maxima at wavelengths λA and λB. The theoretical model of UV-Vis spectrum of molecule X is presented in Fig. 4.1.2. To selectively enhance the vibrations of the chromophore A in a complex spectrum of the molecule, the exciting line has to have ν0 near to νA (which corresponds properly to λA) . Vibrations of chromophore B will be enhanced when the laser wavelength will be equal to λB. On the other hand, if the exciting line λC is used, the non-resonant Raman spectrum which comes from all parts of molecule will be observed.

For this reason, the UV–Vis electronic absorption spectrum of the studied compound, which shows the allowed electronic transitions will help us to choose the best laser wavelength in order to observe the vibrations of specific chromophore. By changing the excitation wavelength, the different RRS of the same molecule may be obtained and give us information about specific parts of the molecule. Such selective enhancement suggests a high specificity of the RRS technique.

The detailed information about UV-Vis spectrum may provide additional information about the RRS origin. The quantitative description of RRS scattering theory was provided by Albrecht et al., who showed how RRS intensity can arise from several mechanisms, mainly from A-term (Franck–Condon) and B-term (Herzberg– –Teller vibronic coupling) [5-7].

In type A or Franck–Condon scattering, only totally symmetric modes are enhanced in RRS. Such mechanism is observed for many compounds. As an example we can include here the RR spectra of TiI₄ and NH₃ obtained by 514.5 and 216.8 nm excitations, respectively [1]. Non–Condon dependence of the electronic transition moment upon the vibrational coordinate is possible in B–term enhancement, where both symmetric and non-symmetric fundamentals can be enhanced. However, the magnitude of B-term enhancement of symmetric vibrations is lower than that of A-term enhancement. B-term enhancement will dominate only for non-symmetric vibrations [8]. Such RR scattering [9] involves vibronic coupling between the two allowed excited electronic transitions. This mechanism is observed for metalloproteins being excited with the laser wavelength which corresponds to the electronic transitions of the Q band of the UV-Vis spectrum. If the enhancement of fundamentals cannot occur via A or B-terms, as transition is rigorously forbidden at the equilibrium geometry, then C-term enhancement of overtones and combinations modes may occur [8,10].

4.1.3. Application and potential of RRS

As we proved above, RRS is characterized by high sensitivity and selectivity in comparison with NR, which gives RRS technique the advantage in many analytical studies. Similar to NR, RRS allows for the study of samples in the gaseous, liquid and solid state.

In art history, archaeology and forensics RRS is successfully used to study the composition of different pigments and dyes. It is also known as a non-invasive and non-destructive method of assessing the distribution and concentration of various biomolecules inside plant and animal tissues. It has been applied to study the carotenoid status in human skin, as a biomarker of fruit/vegetable intake [11]. A single RRS skin measure allowed for the classification of inter-individual variability in skin carotenoid status and to identify factors associated with the biomarker in this population [12]. It is also possible to differentiate various retinoid fractions from a mixture with the use of this technique utilizing different excitation wavelengths. Upon excitations with different wavelengths it was possible to differentiate lutein, violaxanthin, β-carotene and 9-cis neoxanthin [13]. The use of the 532 nm excitation laser line, which allows observation of the pre-resonance Raman spectrum of retinols, was also used to study the distribution of vitamin A component in liver and lung tissues [14-15].

Resonance Raman spectroscopy has long been applied to monitor the molecular dynamics of different metalloproteins, among which the most common is hemoglobin [16]. This highly symmetrical and chromophoric heme prosthetic group provides strong resonance enhancement, especially when the excitation wavelength is in resonance with the intense electronic transitions cantered at ~400 nm (Soret), 525 nm (Qv or α band) and 575 nm (Q₀ or β band) [17]. Moreover, peptide chains of heme proteins may also be studied with this technique as they exhibit transitions below 250 nm. RRS was successfully used not only for standard hemoporphirins, but also for the detection, analysis and visualization of 2D and 3D distributions of heme in both cells and tissues [18,19]. RRS provides excellent signal–to–noise ratio spectra with very high reproducibility from single erythrocytes, which allows for the study of various hemopathies [20].

As in case of heme proteins, peptide chains of other proteins, or protein–drug interactions, may also be studied with the use of excitation sources below 260 nm. The use of RRS in such deep UV was successfully applied in order to investigate DNA, RNA and nucleic acid components [21,22]. The use of RRS in such deep UV is mainly used in the bioanalytical and life science fields, however it is also useful to study solid catalysts and heterogeneous catalytic reactions [23].

Because of the effects of this vibrational technique, information about the electronic structure of a studied sample can be obtained. This makes RRS a very useful technique in nanotechnology and materials science in order to study and characterize structures of such materials as carbon nanotubes, graphite, graphene and others [24,25].

4.1.4. Instrumentation

As already presented and described in Chapter 2, for RRS detection the standard Raman instrumentation may be applied. As mentioned before, selective resonance Raman enhancement of specific chromophores of molecules may be obtained by changing the excitation wavelength. That is why tunable lasers, in which the wavelength can be altered within a specific range, are commonly applied to this technique. To provide positive identification, even with higher than RRS sensitivity and selectivity, RRS is successfully used in combination with liquid chromatography [26] and SERS (surface-enhanced resonance Raman scattering, SERRS). Tip-enhanced Raman spectroscopy (TERS), which is a variation of SERS, may also use the resonance effect (TERRS) and is a promising technique for future nanoanalysis [27].

References

Ferraro J.R., Nakamoto K., Introductory Raman Spectroscopy, Academic Press Inc., San Diego 1994.

Matousek P., Towrie M., Parker A.W., Fluorescence background suppression in Raman spectroscopy using combined Kerr gated and shifted excitation Raman difference techniques, J. Raman Spectrosc., 33, 238 (2002).

Marzec K.M., Wróbel T.P., Ryguła A., Maslak E., Jasztal A., Fedorowicz A., Chlopicki S., Barańska M., Visualization of the biochemical markers of atherosclerotic plaque with the use of Raman, IR and AFM, J. Biophotonics, 7, 744 (2014).

Krishnan R.S., Shankar R.K., Raman effect: History of the discovery, J. Raman Spectrosc., 10, 1 (1981).

Albrecht A.C., On the theory of Raman intensities, J. Chem. Phys., 34, 1476 (1961).

Albrecht A.C. and Hutley M.C., On the Dependence of Vibrational Raman. Intensity on the Wavelength of Incident Light, J. Chem. Phys., 55, 4438 (1971).

Tang J., Albrecht A.C., Raman Spectroscopy: Theory and Practice (eds. H. A. Szymanski) Plenum, New York 1970, 2, pp. 33–68.

Asher S.A., UV resonance Raman studies of molecular structure and dynamics: applications in physical and biophysical chemistry, Anun. Rev. Phys. Chem., 39, 537 (1988).

Wang J., Takahashi S., Rousseau D.L., Identification of the overtone of the Fe–CO stretching mode in heme proteins: a probe of the heme active site, Proc. Natl. Acad. Sci., 92, 9402 (1995).

Marzec K.M., Perez–Guaita D., De Veij M., McNaughton D., Barańska M., Dixon M.W.A., Tilley L., Wood B.R., Red Blood Cells Polarize Green Laser Light Revealing Hemoglobin’s Enhanced Non–Fundamental Raman Modes, Chem. Phys. Chem., 15, 3963 (2014).

Scarmo S., Cartmel B., Lin H., Leffell D.J., Ermakov I.V., Gellermann W., Bernstein P.S., Mayne S.T., Single v. multiple measures of skin carotenoids by resonance Raman spectroscopy as a biomarker of usual carotenoid status, Br. J. Nutr., 110, 911 (2013).

Scarmo S., Henebery K., Peracchio H., Cartmel B., Lin H., Ermakov I.V., Gellermann W., Bernstein P.S., Duffy V.B., Mayne S.T., Skin carotenoid status measured by resonance Raman spectroscopy as a biomarker of fruit and vegetable intake in preschool children, Eur. J. Clin. Nutr., 66, 555 (2012).

Andreeva A., Velitchkova M., Resonance Raman spectroscopy of carotenoids in Photosystem I particles, Biophysical Chemistry, 114, 129 (2005).

Kochan K., Marzec K.M., Chruszcz–Lipska K., Jasztal A., Maslak E., Musiolik H., Chlopicki S., Barańska M., Pathological changes in the biochemical profile of the liver in atherosclerosis and diabetes assessed by Raman spectroscopy, Analyst, 138, 3885 (2013).

Marzec K.M., Kochan K., Fedorowicz A., Jasztal A., Chruszcz–Lipska K., Dobrowolski J. Cz., Chlopicki S., Barańska M., Raman microimaging of murine lungs: insight into the vitamin A content, Analyst, 140, 2171 (2015).

Spiro T.G., Biological Applications of Raman Spectroscopy: Resonance Raman Spectra of Heme and Metalloproteins Vol. 3 John Wiley & Sons, New York 1988.

Yamamoto T., Palmer G., The valence and spin state of iron in oxyhemoglobin as inferred from resonance Raman spectroscopy, J. Biol. Chem., 248, 5211 (1973).

Marzec K.M., Ryguła A., Wood B.R., Chlopicki S., Barańska M., High-resolution Raman imaging reveals spatial location of heme oxidation sites in single red blood cells of dried smears, J. Raman Spectrosc., 46, 76 (2015).

Wood B.R., Caspers P., Puppels G.J., Pandiancherri S., McNaughton D., Resonance Raman spectroscopy of red blood cells using near–infrared laser excitation, Anal. Bioanal. Chem., 387, 1691 (2007).

Wood B.R., McNaughton D., Vibrational Spectroscopy for Medical Diagnosis, (eds. M. Diem, P. R. Griffiths, J.M. Chalmers) John Wiley & Sons, UK 2008, pp. 261–309.

Blazej D.C., Peticolas W.L., Ultraviolet resonant Raman Spectroscopy ofnucleicacidcomponents, Proc. Nati. Acad. Sci., 74, 2639 (1977).

Wojtuszewski K., Mukerji I., The HU–DNA binding interaction probed with UV resonance Raman spectroscopy: Structural elements of specificity, Protein Sci., 13, 2416 (2004).

Kim H., Kosuda K.M., Van Duyne K.P., Stair P.C., Resonance Raman and surface– and tip–enhanced Raman spectroscopy methods to study solid catalysts and heterogeneous catalytic reactions, Chem. Soc. Rev., 39, 4820 (2010).

Jorio A., Pimenta M.A., Souza Filho A.G., Saito R., Dresselhaus G., Dresselhaus M.S., Characterizing carbon nanotube samples with resonance Raman scattering, New. Phys., 5, 139.1 (2003).

Zolyomi V., Koltai J. and Kurti J., Resonance Raman spectroscopy of graphite and graphene, Phys. Status Solidi B, 248, 2435 (2011).

Dijkstra R.J., Ariese F., Gooijer C., Brinkman U.A.Th., Raman spectroscopy as a detection method for liquid–separation techniques, TrAC, 24, 304 (2005).

Taguchi A., Hayazawa N., Furusawa K., Ishitobi H., Kawata S., Deep–UV tip–enhanced Raman scattering, J. Raman Spectrosc., 40, 1324 (2009).