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The ability of a chemically treated plastic or other transparent material to darken reversibly in strong light.
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.



the ability of a substance to undergo a reversible transformation, upon exposure to optical radiation, from one state to any other state in which an optical absorption spectrum appears or changes markedly in the substance. A reversible transformation is a transformation in which a substance later reverts to its initial state. Many substances undergo such reversible transformations when exposed to, for example, X rays or microwaves. Nevertheless, such substances are photochromic in the strict sense only if they undergo reversible transformations upon exposure to ultraviolet, visible, or infrared radiation.

A general description of the photochromic process follows. In the initial state A, a substance, having absorbed optical radiation of a specific spectral composition, undergoes a transformation to a light-induced state B, which is characterized by a different absorption spectrum and a certain lifetime that is specific for a given state. The reverse transformation BA occurs spontaneously as a result of heat energy and may be accelerated to an extremely high degree when the substance is heated or absorbs light in state B.

Photochromism is characteristic of a very large number of organic and inorganic substances. The photochromism of organic substances is based on several photophysical processes or numerous photochemical reactions. If photochromism is based on photochemical reactions, the reactions are accompanied either by a rearrangement of valence bonds or by a change in the configuration of the atoms in the molecules, which is known as cis-trans isomerism (seeISOMERISM). Valence bonds are rearranged during, for example, dissociation, dimerization, the rearrangement of atoms in a molecule, oxidation-reduction reactions, or tautomeric transformations (seeTAUTOMERISM). The photochromism of inorganic substances is caused by various processes, such as reversible light-induced electron transfer (which results in the appearance of various types of color centers and in a change in the valence of metal ions) or reversible photodissociation reactions.

Photochromic materials have been developed on the basis of organic and inorganic photochromic substances. The use of photochromic materials in science and technology depends on the photosensitivity of the materials, the reversibility of the photophysical and photochemical processes that occur in the materials, the appearance or change of color or absorption spectra immediately upon exposure to light, and differences in the thermal, chemical, and physical properties of the initial and light-induced states of the photochromic substances.


Terenin, A. N. Fotonika molekul krasitelei i rodstvennykh organicheskikh soedinenii. Leningrad, 1967.
Barachevskii, V. A. “Fotokhromizm.” Zhurnal Vsesoiuznogo Khimicheskogo ob-va im. D. I. Mendeleeva, 1974, vol. 19, no. 4, pp. 423–33.
Barachevskii, V. A., G. I. Lashkov, and V. A. Tsekhomskii. Fotokhromizm i ego primenenie. Moscow, 1977.
Photochromism. New York [1971].


The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.
References in periodicals archive ?
Irradiation of azomethine imine 1-4 O solutions in acetonitrile with light of [[lambda].sub.irr] 365 nm results in spectral changes in the characteristic of negative photochromism due to intramolecular photocyclization into diaziridines 1-4 C (Scheme 2), accompanied by a decrease in the intensity of long-wave absorption maxima and the appearance of absorption bands in the short-wave region of the spectrum [10, 30, 31] as shown in Figure 2(a) in the example of compound 1 and in Table 1.
Photochromism is the term used for a reversible photo induced transformation of a molecule between two isomers whose absorption spectra are distinguishably different (Durr and Bouas-Laurent, 1990).
Kawato, "Crystalline photochromism of N-salicylidene-2,6-dialkylanilines: advantage of 2,6-dialkyl substituents of aniline for preparation of photochromic Schiff base crystals," Organic & Biomolecular Chemistry, vol.
(2003) Optically switchable molecular solids: Photoinduced spin-crossover, photochromism, and photoinduced magnetization.
Their topics include templating photoreactions in solutions, supramolecular photochirogenesis, the photochromism of multicomponent diarylethene crystals, controlling photoreactions through non-covalent interactions within zeolite nanocages, and protein-controlled ultrafast photoisomerization in rhodopsin and bacteriorhodopsin.
Photochromism is a reversible change in color upon exposure to light.
Photochromism is an interesting and intriguing property of materials.
Photochromism is the phenomenon of color change that occurs when certain substances are exposed to certain radiation wavelengths.
Similarly, the color change shown in different solvents is called as "solvatochromism." Added to this is the input from the branch of photochemistry called photochromism that represents light induced color transitions.
He transferred to the Central Research Division of American Cyanamid in 1960, where he led a group that carried out fundamental studies in strained ring chemistry and in organic photochemistry related to the phenomenon of photochromism. In 1966 Syntex Corp.
Among the various forms of tungsten materials, tungsten oxides are important semiconductors, which can be used in solar-driven photo catalysis [1-3], electrochromism [4], and photochromism [5].