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Also known as:
Anna J. Harrison
Born:
Dec. 23, 1912, Benton City, Mo., U.S.
Died:
Aug. 8, 1998, Holyoke, Mass. (aged 85)

Anna Jane Harrison (born Dec. 23, 1912, Benton City, Mo., U.S.—died Aug. 8, 1998, Holyoke, Mass.) was an American chemist and educator who in 1978 became the first woman president of the American Chemical Society. She was known for her advocacy for increased public awareness of science.

Harrison grew up on a farm in rural Missouri. Her father died when she was seven, leaving her mother to manage the family farm and to care for Harrison and her elder brother. Harrison’s formative education took place in a one-room schoolhouse near her home. She later attended high school in a nearby town. Harrison’s intellectual interests eventually led her to the University of Missouri, where she earned a bachelor’s degree in 1933. She then returned to her hometown to teach at the same rural one-room school she had attended in her youth. Two years later, however, she resumed studies at the university, this time as a graduate student in physical chemistry. After receiving a master’s degree in 1937, she published a paper on photovoltaic effects (voltages generated by interactions between dissimilar chemicals when struck by light) in solutions of Grignard reagents (organic derivatives of magnesium). She also began work toward a doctorate, which she earned in 1940. Her dissertation research focused on the association of sodium ketyls (a type of radical).

Upon completing her doctorate studies, Harrison took a post as an instructor of chemistry at H. Sophie Newcomb Memorial College, a women’s college at Tulane University in New Orleans. Over the course of the next several years, she also performed research for the National Defense Research Council and for Corning Glass Works and continued to study ketyl association. In 1945 she joined the faculty at Mount Holyoke College, a women’s school in South Hadley, Mass., where she was elevated to full professor in 1950 and was chair of the department of chemistry from 1960 to 1966. At Mount Holyoke, Harrison contributed to research on ultraviolet light and photolysis, or the breakdown of molecules via light absorption.

Michael Faraday (L) English physicist and chemist (electromagnetism) and John Frederic Daniell (R) British chemist and meteorologist who invented the Daniell cell.
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In the 1970s Harrison became increasingly outspoken about the need for improving the communication of science to the public and in particular to public officials. Following her election as president of the American Chemical Society, she continued to champion the importance of cultivating a scientifically informed public. She encouraged her colleagues to view the chemical profession as fundamental to not only the advancement of scientific knowledge but also the improvement of science education, public awareness of science, and public welfare.

In 1979 Harrison retired from Mount Holyoke. However, she remained active in promoting the communication of science and served on multiple scientific councils. From 1983 to 1984 she was president of the American Association for the Advancement of Science (AAAS), and in 1989, with former Mount Holyoke colleague Edwin S. Weaver, she published Chemistry: A Search to Understand. The authors described the work as suited for students who were “intellectually curious but not professionally driven” in the field of chemistry. Harrison received many honours throughout her career and was celebrated for having inspired numerous young women to pursue careers in science.

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spectroscopy, study of the absorption and emission of light and other radiation by matter, as related to the dependence of these processes on the wavelength of the radiation. More recently, the definition has been expanded to include the study of the interactions between particles such as electrons, protons, and ions, as well as their interaction with other particles as a function of their collision energy. Spectroscopic analysis has been crucial in the development of the most fundamental theories in physics, including quantum mechanics, the special and general theories of relativity, and quantum electrodynamics. Spectroscopy, as applied to high-energy collisions, has been a key tool in developing scientific understanding not only of the electromagnetic force but also of the strong and weak nuclear forces.

Spectroscopic techniques have been applied in virtually all technical fields of science and technology. Radio-frequency spectroscopy of nuclei in a magnetic field has been employed in a medical technique called magnetic resonance imaging (MRI) to visualize the internal soft tissue of the body with unprecedented resolution. Microwave spectroscopy was used to discover the so-called three-degree blackbody radiation, the remnant of the big bang (i.e., the primeval explosion) from which the universe is thought to have originated (see below Survey of optical spectroscopy: General principles: Applications). The internal structure of the proton and neutron and the state of the early universe up to the first thousandth of a second of its existence are being unraveled with spectroscopic techniques using high-energy particle accelerators. The constituents of distant stars, intergalactic molecules, and even the primordial abundance of the elements before the formation of the first stars can be determined by optical, radio, and X-ray spectroscopy. Optical spectroscopy is used routinely to identify the chemical composition of matter and to determine its physical structure.

Spectroscopic techniques are extremely sensitive. Single atoms and even different isotopes of the same atom can be detected among 1020 or more atoms of a different species. (Isotopes are all atoms of an element that have unequal mass but the same atomic number. Isotopes of the same element are virtually identical chemically.) Trace amounts of pollutants or contaminants are often detected most effectively by spectroscopic techniques. Certain types of microwave, optical, and gamma-ray spectroscopy are capable of measuring infinitesimal frequency shifts in narrow spectroscopic lines. Frequency shifts as small as one part in 1015 of the frequency being measured can be observed with ultrahigh resolution laser techniques. Because of this sensitivity, the most accurate physical measurements have been frequency measurements.

Spectroscopy now covers a sizable fraction of the electromagnetic spectrum. The table summarizes the electromagnetic spectrum over a frequency range of 16 orders of magnitude. Spectroscopic techniques are not confined to electromagnetic radiation, however. Because the energy E of a photon (a quantum of light) is related to its frequency ν by the relation E = hν, where h is Planck’s constant, spectroscopy is actually the measure of the interaction of photons with matter as a function of the photon energy. In instances where the probe particle is not a photon, spectroscopy refers to the measurement of how the particle interacts with the test particle or material as a function of the energy of the probe particle.

Electromagnetic phenomena
approximate wavelength range (metres) approximate frequency range (hertz)
radio waves 10–1,000 3 × 105–3 × 107
television waves 1–10 3 × 107–3 × 108
microwaves, radar 1 × 10−3–1 3 × 108–3 × 1011
infrared 8 × 10−7–1 × 10−3 3 × 1011–4 × 1014
visible light 4 × 10−7–7 × 10−7 4 × 1014–7 × 1014
ultraviolet 1 × 10−8–4 × 10−7 7 × 1014–3 × 1016
X-rays 5 × 10−12–1 × 10−8 3 × 1016–6 × 1019
gamma rays (γ rays) ﹤5 × 10 -12 >6 × 1019

An example of particle spectroscopy is a surface analysis technique known as electron energy loss spectroscopy (EELS) that measures the energy lost when low-energy electrons (typically 5–10 electron volts) collide with a surface. Occasionally, the colliding electron loses energy by exciting the surface; by measuring the electron’s energy loss, vibrational excitations associated with the surface can be measured. On the other end of the energy spectrum, if an electron collides with another particle at exceedingly high energies, a wealth of subatomic particles is produced. Most of what is known in particle physics (the study of subatomic particles) has been gained by analyzing the total particle production or the production of certain particles as a function of the incident energies of electrons and protons.

The following sections focus on the methods of electromagnetic spectroscopy, particularly optical spectroscopy. Although most of the other forms of spectroscopy are not covered in detail, they have the same common heritage as optical spectroscopy. Thus, many of the basic principles used in other spectroscopies share many of the general features of optical spectroscopy.

Survey of optical spectroscopy

General principles

Basic features of electromagnetic radiation

Electromagnetic radiation is composed of oscillating electric and magnetic fields that have the ability to transfer energy through space. The energy propagates as a wave, such that the crests and troughs of the wave move in vacuum at the speed of 299,792,458 metres per second. The many forms of electromagnetic radiation appear different to an observer; light is visible to the human eye, while X rays and radio waves are not.

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The distance between successive crests in a wave is called its wavelength. The various forms of electromagnetic radiation differ in wavelength. For example, the visible portion of the electromagnetic spectrum lies between 4 × 10−7 and 8 × 10−7 metre (1.6 × 10−5 and 3.1 × 10−5 inch): red light has a longer wavelength than green light, which in turn has a longer wavelength than blue light. Radio waves can have wavelengths longer than 1,000 metres, while those of high-energy gamma rays can be shorter than 10−16 metre, which is one-millionth of the diameter of an atom. Visible light and X rays are often described in units of angstroms or in nanometres. One angstrom (abbreviated by the symbol Å) is 10−10 metre, which is also the typical diameter of an atom. One nanometre (nm) is 10−9 metre. The micrometre (μm), which equals 10−6 metre, is often used to describe infrared radiation.

The decomposition of electromagnetic radiation into its component wavelengths is fundamental to spectroscopy. Evolving from the first crude prism spectrographs that separated sunlight into its constituent colours, modern spectrometers have provided ever-increasing wavelength resolution. Large-grating spectrometers (see below Practical considerations: Methods of dispersing spectra) are capable of resolving wavelengths as close as 10−3 nanometre, while modern laser techniques can resolve optical wavelengths separated by less than 10−10 nanometre.

The frequency with which the electromagnetic wave oscillates is also used to characterize the radiation. The product of the frequency (ν) and the wavelength (λ) is equal to the speed of light (c); i.e., νλ = c. The frequency is often expressed as the number of oscillations per second, and the unit of frequency is hertz (Hz), where one hertz is one cycle per second. Since the electromagnetic spectrum spans many orders of magnitude, frequency units are usually accompanied by a Latin prefix to set the scale of the frequency range. (See measurement system: The metric system of measurement: The International System of Units for a table of the prefixes commonly used to denote these scales.)