Photoisomerization: Difference between revisions

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'''Photoisomerization''' is a process in [[chemistry]] and [[biochemistry]] where the [[isomer]]s of a molecule in a [[chemical compound]] are transformed through the absorption of [[light]]. This process is a key mechanism in the [[vision]] process of many organisms and has significant applications in the field of [[optoelectronics]].
== Photoisomerization ==
 
'''Photoisomerization''' is a process in which a molecule undergoes a structural change upon absorption of light. This phenomenon is a type of [[isomerization]] that is specifically induced by [[photons]], typically in the [[ultraviolet]] or [[visible spectrum]]. Photoisomerization plays a crucial role in various biological processes and technological applications.
 
=== Mechanism ===


== Overview ==
Photoisomerization involves the conversion of a molecule from one [[isomer]] to another. This process is initiated when a molecule absorbs a photon, which provides the energy necessary to overcome the energy barrier between isomers. The absorbed energy excites the molecule from its ground state to an excited state, allowing it to undergo a structural rearrangement.


Photoisomerization involves the rearrangement of a molecule's atoms caused by the absorption of light, resulting in a change in the molecule's [[geometry]]. This process can occur in various types of molecules, including [[organic compound]]s and [[inorganic compound]]s. The two main types of photoisomerization are [[cis-trans isomerism|cis-trans]] and [[conformational isomerism|conformational]] photoisomerization.
[[File:Photoisomerization.svg|thumb|right|300px|Diagram illustrating the photoisomerization process.]]


== Cis-trans Photoisomerization ==
In many cases, the isomerization involves a change in the configuration around a [[double bond]], such as the conversion between [[cis]] and [[trans]] isomers. For example, in the case of [[retinal]], a key molecule in the [[visual cycle]], photoisomerization changes the configuration from 11-cis-retinal to all-trans-retinal, triggering a signal transduction cascade in [[photoreceptor cells]].


Cis-trans photoisomerization involves the rotation around a [[double bond]] in a molecule. The [[cis isomer]] has atoms on the same side of the double bond, while the [[trans isomer]] has atoms on opposite sides. When light is absorbed, the molecule can switch from one form to the other. This process is crucial in the vision process of many organisms, as it occurs in the [[retina]]l molecule found in the [[eye]].
=== Biological Significance ===


== Conformational Photoisomerization ==
Photoisomerization is essential in several biological systems. One of the most well-known examples is the role of retinal in [[vision]]. In the [[retina]], retinal is bound to the protein [[opsin]] to form [[rhodopsin]]. When rhodopsin absorbs light, retinal undergoes photoisomerization, leading to a conformational change in the protein and the initiation of a neural signal to the brain.


Conformational photoisomerization involves the rotation around a [[single bond]] in a molecule. This process can result in a variety of different shapes for the molecule, each with different [[chemical properties]]. Conformational photoisomerization is a key process in many biological systems, including the [[protein folding]] process.
Another example is the photoisomerization of [[phytochromes]] in plants, which are involved in regulating growth and development in response to light. Phytochromes exist in two forms, Pr and Pfr, which interconvert through photoisomerization, allowing plants to sense changes in light conditions.


== Applications ==
=== Technological Applications ===


Photoisomerization has significant applications in the field of optoelectronics, particularly in the development of [[molecular switch]]es and [[data storage]] devices. The ability to control the shape of a molecule using light allows for the creation of devices with unique properties.
Photoisomerization is utilized in various technological applications, including the development of [[molecular switches]] and [[photoresponsive materials]]. These materials can change their properties in response to light, making them useful in [[optical data storage]], [[smart windows]], and [[drug delivery systems]].


== See also ==
[[File:Azobenzene.png|thumb|left|200px|Azobenzene, a common photoisomerizable compound used in molecular switches.]]


* [[Isomer]]
One of the most studied photoisomerizable compounds is [[azobenzene]], which can switch between its trans and cis forms upon exposure to light. This property is exploited in the design of [[photochromic]] devices and [[nanomachines]].
 
== Related Pages ==
* [[Isomerization]]
* [[Photochemistry]]
* [[Photochemistry]]
* [[Photobiology]]
* [[Retinal]]
* [[Optoelectronics]]
* [[Rhodopsin]]
* [[Phytochrome]]
* [[Azobenzene]]


== References ==
{{Photochemistry}}


<references />
[[Category:Chemical reactions]]
[[Category:Photochemistry]]
[[Category:Photochemistry]]
[[Category:Isomerism]]
[[Category:Biochemistry]]
[[Category:Biochemistry]]
[[Category:Optoelectronics]]
{{chemistry-stub}}
{{medicine-stub}}
== Photoisomerization ==
<gallery>
File:AzobenzeneIsom_no_Engl.png|Azobenzene isomerization
File:Methyl_red.svg|Methyl red
File:Synthesis_of_quadricyclane_from_norbornadiene.png|Synthesis of quadricyclane from norbornadiene
File:Cis-trans-PtCl2P2.png|Cis-trans isomerization of PtCl2P2
File:Fe(picNH2)3.png|Fe(picNH2)3
</gallery>

Revision as of 17:42, 18 February 2025

Photoisomerization

Photoisomerization is a process in which a molecule undergoes a structural change upon absorption of light. This phenomenon is a type of isomerization that is specifically induced by photons, typically in the ultraviolet or visible spectrum. Photoisomerization plays a crucial role in various biological processes and technological applications.

Mechanism

Photoisomerization involves the conversion of a molecule from one isomer to another. This process is initiated when a molecule absorbs a photon, which provides the energy necessary to overcome the energy barrier between isomers. The absorbed energy excites the molecule from its ground state to an excited state, allowing it to undergo a structural rearrangement.

File:Photoisomerization.svg
Diagram illustrating the photoisomerization process.

In many cases, the isomerization involves a change in the configuration around a double bond, such as the conversion between cis and trans isomers. For example, in the case of retinal, a key molecule in the visual cycle, photoisomerization changes the configuration from 11-cis-retinal to all-trans-retinal, triggering a signal transduction cascade in photoreceptor cells.

Biological Significance

Photoisomerization is essential in several biological systems. One of the most well-known examples is the role of retinal in vision. In the retina, retinal is bound to the protein opsin to form rhodopsin. When rhodopsin absorbs light, retinal undergoes photoisomerization, leading to a conformational change in the protein and the initiation of a neural signal to the brain.

Another example is the photoisomerization of phytochromes in plants, which are involved in regulating growth and development in response to light. Phytochromes exist in two forms, Pr and Pfr, which interconvert through photoisomerization, allowing plants to sense changes in light conditions.

Technological Applications

Photoisomerization is utilized in various technological applications, including the development of molecular switches and photoresponsive materials. These materials can change their properties in response to light, making them useful in optical data storage, smart windows, and drug delivery systems.

Azobenzene, a common photoisomerizable compound used in molecular switches.

One of the most studied photoisomerizable compounds is azobenzene, which can switch between its trans and cis forms upon exposure to light. This property is exploited in the design of photochromic devices and nanomachines.

Related Pages

Template:Photochemistry