Molar attenuation coefficient

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In chemistry, the molar attenuation coefficient or molar absorption coefficient [1] is a measurement of how strongly a chemical species absorbs, and thereby attenuates, light at a given wavelength. It is an intrinsic property of the species. The SI unit of molar attenuation coefficient is the square metre per mole (m2/mol), but in practice, quantities are usually expressed in terms of M −1⋅cm−1 or L⋅mol−1⋅cm−1 (the latter two units are both equal to 0.1 m2/mol). In older literature, the cm2/mol is sometimes used; 1 M−1⋅cm−1 equals 1000 cm2/mol. The molar attenuation coefficient is also known as the molar extinction coefficient, and molar absorptivity, but the use of these alternative terms has been discouraged by the IUPAC. [2] [3]

Contents

Beer–Lambert law

The absorbance of a material that has only one attenuating species also depends on the pathlength and the concentration of the species, according to the Beer–Lambert law

where

Different disciplines have different conventions as to whether absorbance is decadic (10-based) or Napierian (e-based), i.e., defined with respect to the transmission via common logarithm (log10) or a natural logarithm (ln). The molar attenuation coefficient is usually decadic. [1] [4] When ambiguity exists, it is best to indicate which one applies.

When there are N attenuation species in a solution, the overall absorbance is the sum of the absorbances for each individual species i:

The composition of a mixture of N attenuating species can be found by measuring the absorbance at N wavelengths (the values of the molar coefficient of attenuation for each species at these wavelengths must also be known). The wavelengths chosen are usually the wavelengths of maximum absorption (absorbance maxima) for the individual species. None of the wavelengths must be an isosbestic point for a pair of species. The set of the following simultaneous equations can be solved to find the concentrations of each attenuating species:

The molar attenuation coefficient (in units of cm2) is directly related to the attenuation cross section via the Avogadro constant NA: [5]

Mass attenuation coefficient

The mass attenuation coefficient is equal to the molar attenuation coefficient divided by the molar mass.

Proteins

In biochemistry, the molar attenuation coefficient of a protein at 280 nm depends almost exclusively on the number of aromatic residues, particularly tryptophan, and can be predicted from the sequence of amino acids. [6] Similarly, the extinction coefficient of nucleic acids at 260 nm can be predicted given the nucleotide sequence.

If the molar attenuation coefficient is known, it can be used to determine the concentration of a protein in solution.

Related Research Articles

<span class="mw-page-title-main">Beer–Lambert law</span> Law describing absorption of light

The Beer–Lambert law, also known as Beer's law, the Lambert–Beer law, or the Beer–Lambert–Bouguer law relates the attenuation of light to the properties of the material through which the light is travelling. The law is commonly applied to chemical analysis measurements and used in understanding attenuation in physical optics, for photons, neutrons, or rarefied gases. In mathematical physics, this law arises as a solution of the BGK equation.

In physics, the cross section is a measure of the probability that a specific process will take place when some kind of radiant excitation intersects a localized phenomenon. For example, the Rutherford cross-section is a measure of probability that an alpha particle will be deflected by a given angle during an interaction with an atomic nucleus. Cross section is typically denoted σ (sigma) and is expressed in units of area, more specifically in barns. In a way, it can be thought of as the size of the object that the excitation must hit in order for the process to occur, but more exactly, it is a parameter of a stochastic process.

<span class="mw-page-title-main">Refractive index</span> Ratio of the speed of light in vacuum to that in the medium

In optics, the refractive index of an optical medium is a dimensionless number that gives the indication of the light bending ability of that medium.

<span class="mw-page-title-main">Optical depth</span>

In physics, optical depth or optical thickness is the natural logarithm of the ratio of incident to transmitted radiant power through a material. Thus, the larger the optical depth, the smaller the amount of transmitted radiant power through the material. Spectral optical depth or spectral optical thickness is the natural logarithm of the ratio of incident to transmitted spectral radiant power through a material. Optical depth is dimensionless, and in particular is not a length, though it is a monotonically increasing function of optical path length, and approaches zero as the path length approaches zero. The use of the term "optical density" for optical depth is discouraged.

Circular dichroism (CD) is dichroism involving circularly polarized light, i.e., the differential absorption of left- and right-handed light. Left-hand circular (LHC) and right-hand circular (RHC) polarized light represent two possible spin angular momentum states for a photon, and so circular dichroism is also referred to as dichroism for spin angular momentum. This phenomenon was discovered by Jean-Baptiste Biot, Augustin Fresnel, and Aimé Cotton in the first half of the 19th century. Circular dichroism and circular birefringence are manifestations of optical activity. It is exhibited in the absorption bands of optically active chiral molecules. CD spectroscopy has a wide range of applications in many different fields. Most notably, UV CD is used to investigate the secondary structure of proteins. UV/Vis CD is used to investigate charge-transfer transitions. Near-infrared CD is used to investigate geometric and electronic structure by probing metal d→d transitions. Vibrational circular dichroism, which uses light from the infrared energy region, is used for structural studies of small organic molecules, and most recently proteins and DNA.

<span class="mw-page-title-main">Magnetic circular dichroism</span>

Magnetic circular dichroism (MCD) is the differential absorption of left and right circularly polarized light, induced in a sample by a strong magnetic field oriented parallel to the direction of light propagation. MCD measurements can detect transitions which are too weak to be seen in conventional optical absorption spectra, and it can be used to distinguish between overlapping transitions. Paramagnetic systems are common analytes, as their near-degenerate magnetic sublevels provide strong MCD intensity that varies with both field strength and sample temperature. The MCD signal also provides insight into the symmetry of the electronic levels of the studied systems, such as metal ion sites.

<span class="mw-page-title-main">Sellmeier equation</span> Empirical relationship between refractive index and wavelength

The Sellmeier equation is an empirical relationship between refractive index and wavelength for a particular transparent medium. The equation is used to determine the dispersion of light in the medium.

<span class="mw-page-title-main">Wavenumber</span> Spatial frequency of a wave

In the physical sciences, the wavenumber is the spatial frequency of a wave, measured in cycles per unit distance or radians per unit distance. It is analogous to temporal frequency, which is defined as the number of wave cycles per unit time or radians per unit time.

Absorbance is defined as "the logarithm of the ratio of incident to transmitted radiant power through a sample ". Alternatively, for samples which scatter light, absorbance may be defined as "the negative logarithm of one minus absorptance, as measured on a uniform sample". The term is used in many technical areas to quantify the results of an experimental measurement. While the term has its origin in quantifying the absorption of light, it is often entangled with quantification of light which is “lost” to a detector system through other mechanisms. What these uses of the term tend to have in common is that they refer to a logarithm of the ratio of a quantity of light incident on a sample or material to that which is detected after the light has interacted with the sample. 

<span class="mw-page-title-main">Isosbestic point</span> Spectroscopic property in chemical reactions

In spectroscopy, an isosbestic point is a specific wavelength, wavenumber or frequency at which the total absorbance of a sample does not change during a chemical reaction or a physical change of the sample. The word derives from two Greek words: "iso", meaning "equal", and "sbestos", meaning "extinguishable".

<span class="mw-page-title-main">Transmittance</span> Ratio of transmitted to incident radiant flux

Transmittance of the surface of a material is its effectiveness in transmitting radiant energy. It is the fraction of incident electromagnetic power that is transmitted through a sample, in contrast to the transmission coefficient, which is the ratio of the transmitted to incident electric field.

The Standard Reference Method or SRM is one of several systems modern brewers use to specify beer color. Determination of the SRM value involves measuring the attenuation of light of a particular wavelength (430 nm) in passing through 1 cm of the beer, expressing the attenuation as an absorption and scaling the absorption by a constant.

<span class="mw-page-title-main">Absorption cross section</span>

Absorption cross section is a measure for the probability of an absorption process. More generally, the term cross section is used in physics to quantify the probability of a certain particle-particle interaction, e.g., scattering, electromagnetic absorption, etc. In honor of the fundamental contribution of Maria Goeppert Mayer to this area, the unit for the two-photon absorption cross section is named the "GM". One GM is 10−50 cm4⋅s⋅photon−1.

Equilibrium constants are determined in order to quantify chemical equilibria. When an equilibrium constant K is expressed as a concentration quotient,

The linear attenuation coefficient, attenuation coefficient, or narrow-beam attenuation coefficient characterizes how easily a volume of material can be penetrated by a beam of light, sound, particles, or other energy or matter. A coefficient value that is large represents a beam becoming 'attenuated' as it passes through a given medium, while a small value represents that the medium had little effect on loss. The SI unit of attenuation coefficient is the reciprocal metre (m−1). Extinction coefficient is another term for this quantity, often used in meteorology and climatology. Most commonly, the quantity measures the exponential decay of intensity, that is, the value of downward e-folding distance of the original intensity as the energy of the intensity passes through a unit thickness of material, so that an attenuation coefficient of 1 m−1 means that after passing through 1 metre, the radiation will be reduced by a factor of e, and for material with a coefficient of 2 m−1, it will be reduced twice by e, or e2. Other measures may use a different factor than e, such as the decadic attenuation coefficient below. The broad-beam attenuation coefficient counts forward-scattered radiation as transmitted rather than attenuated, and is more applicable to radiation shielding.

The mass attenuation coefficient, or mass narrow beam attenuation coefficient of a material is the attenuation coefficient normalized by the density of the material; that is, the attenuation per unit mass. Thus, it characterizes how easily a mass of material can be penetrated by a beam of light, sound, particles, or other energy or matter. In addition to visible light, mass attenuation coefficients can be defined for other electromagnetic radiation, sound, or any other beam that can be attenuated. The SI unit of mass attenuation coefficient is the square metre per kilogram. Other common units include cm2/g and mL⋅g−1⋅cm−1. Mass extinction coefficient is an old term for this quantity.

When an electromagnetic wave travels through a medium in which it gets attenuated, it undergoes exponential decay as described by the Beer–Lambert law. However, there are many possible ways to characterize the wave and how quickly it is attenuated. This article describes the mathematical relationships among:

Free carrier absorption occurs when a material absorbs a photon, and a carrier is excited from an already-excited state to another, unoccupied state in the same band. This intraband absorption is different from interband absorption because the excited carrier is already in an excited band, such as an electron in the conduction band or a hole in the valence band, where it is free to move. In interband absorption, the carrier starts in a fixed, nonconducting band and is excited to a conducting one.

The near-infrared (NIR) window defines the range of wavelengths from 650 to 1350 nanometre (nm) where light has its maximum depth of penetration in tissue. Within the NIR window, scattering is the most dominant light-tissue interaction, and therefore the propagating light becomes diffused rapidly. Since scattering increases the distance travelled by photons within tissue, the probability of photon absorption also increases. Because scattering has weak dependence on wavelength, the NIR window is primarily limited by the light absorption of blood at short wavelengths and water at long wavelengths. The technique using this window is called NIRS. Medical imaging techniques such as fluorescence image-guided surgery often make use of the NIR window to detect deep structures.

A variable pathlength cell is a sample holder used for ultraviolet–visible spectroscopy or infrared spectroscopy that has a path length that can be varied to change the absorbance without changing the sample concentration.

References

  1. 1 2 "Chapter 11 Section 2 - Terms and symbols used in photochemistry and in light scattering" (PDF). Compendium on Analytical Nomenclature (Orange Book). IUPAC. 2002. p. 28.
  2. IUPAC , Compendium of Chemical Terminology , 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006) " Extinction ". doi : 10.1351/goldbook.E02293
  3. IUPAC , Compendium of Chemical Terminology , 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006) " Absorptivity ". doi : 10.1351/goldbook.A00044
  4. "Molecular Spectroscopy" (PDF). Compendium on Analytical Nomenclature. IUPAC. 2002. "Measuring techniques" (PDF). Compendium on Analytical Nomenclature. IUPAC. 2002.
  5. Lakowicz, J. R. (2006). Principles of Fluorescence Spectroscopy (3rd ed.). New York: Springer. p. 59. ISBN   9780387312781.
  6. Gill, S. C.; von Hippel, P. H. (1989). "Calculation of protein extinction coefficients from amino acid sequence data". Analytical Biochemistry. 182 (2): 319–326. doi:10.1016/0003-2697(89)90602-7. PMID   2610349.