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Molecular switch

Molecular switch is a chemistry topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Molecular switch rather than just read about it. In short: A molecular switch is a molecule that can be switched between two or more stable or metastable states with the use of any external (exogenous) or internal (endogenous) stimuli, such as changes in pH, light, temperature, an electric current, a microenvironment, or in the presence of ions, and other ligands. In some cases, a combination of stimuli is required.

Molecular switch — main illustration
Molecular switch — illustration

Key takeaways

  • Molecular switch belongs to chemistry; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Molecular switch to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Molecular switch from memory before moving on to harder problems.

Reference excerpt

A molecular switch is a molecule that can be switched between two or more stable or metastable states with the use of any external (exogenous) or internal (endogenous) stimuli, such as changes in pH, light, temperature, an electric current, a microenvironment, or in the presence of ions, and other ligands. In some cases, a combination of stimuli is required. Molecular switches are reversible. They have been considered for a wide area of possible applications, but the main uses are in photochromic lenses and windows.

Biological Biological stimuli are endogenous form of stimuli. This involves variation in the physiological changes around the cells, such as variable pH, presence of oxidative or reductive species, and enzymes. In cellular biology, proteins act as intracellular signaling molecules by activating another protein in a signaling pathway. In order to do this, proteins act as molecular switches by toggling between active and inactive states. For example, phosphorylation of proteins can be used to activate or inactivate proteins. The external signal flipping the molecular switch could be a protein kinase, which adds a phosphate group to the protein, or a protein phosphatase, which removes phosphate groups. Normal tissues and diseased tissues have different pH, so current approaches of effective drug delivery systems (DDS) include the use of this difference in pH as an endogenous stimulus. Such DDS offer a huge advantage over the conventional therapeutic drug release methods as they selectively release drug cargo at a specific physiological pH. For instance, a study by Shi et al. proposed a pH-responsive/enzyme-cascade-reactive nanoplatform for antibacterial applications. Many artificial nucleic acid-based switches have opened up new opportunities in nucleic-acid nanoscience and RNA/DNA biochemistry.

Acidochromic The ability of some compounds to change color in function of the pH was known since the sixteenth century. This effect was even known before the development of acid-base theory. Those are found in a wide range of plants like roses, cornflowers, primroses and violets. Robert Boyle was the first person to describe this effect, employing plant juices (in the forms of solution and impregnated paper). This effect is the result of structural or electronic changes in molecules upon interaction with protons and is called acidochromism. Acidochromic molecules are most commonly used as pH indicators such as phenolphthalein, methyl orange, and methyl red. Their acidic and basic forms have different colors. When an acid or a base is added, the equilibrium between the two forms is displaced.

Examples in the literature of molecular switches with reversible pH response are spiropyran, hydrazones, Donor-Acceptor-Steenhouse Aduucts (DASA), heptamethine–oxonol dyes, etc. Spiropyran, SP changes its color from blue in the presence of acid such as TFA (trifluroacetic acid) to colorless ring opened form called merocyanine, MC while under alkaline conditions reverts it back to the ring closed, SP form. They are called dual responsive switches since light can also be used to trigger the isomerization. There mechanism of isomerization is shown in the figure above. Due to their easy synthesis and excellent optical stability, they are widely used in bioimaging and pH sensing. An interesting example of pH-responsive molecular switches is shown by Yin's group, who developed pH sensors made up of the spiropyran-based fluorescent probe that can be used for precise and rapid pH detection by making their pH paper strips. Their probe also incorporates indole salts as nucleophilic addition sites that react with OH− ions (hydroxide ions) in different pH environments. A 2022 report by Wang et al. shows the spiropyran-based cellulose nanocrystals useful for pH sensors.

Acidochromic behavior of hydrazones (C=N-N-) is attributed to their tautomerization under an acidic or basic conditions. This linkage is useful in drug delivery (DDS) due to their faster hydrolysis rate in an acidic environment. Acid can also help to tune the physical state of the switch. In 2022, Quintard and coworkers have shown the sol- gel transition of various amines using trichloroacetic acid (TCA) as fuel to create new types of time-controlled smart materials.

Photochromic

The molecules that isomerize when exposed to light of suitable wavelength are called photoswitches. Members of this class include azobenzenes, diarylethenes, dithienylethenes, fulgides, stilbenes, norbornadiene, spiropyrans, hydrazones, indigoids, diazocines, and phenoxynaphthacene quinones. The inspiration to study light-sensitive switches came from an understanding of retinal. In the dark, retinal exists primarily in an all-trans configuration, except for a cis bond at C-11. Upon exposure to light, it undergoes photoisomerization to an all-trans configuration. Photo-induced structural, physical, or chemical changes can involve isomerization of bonds (cis ↔ trans), electron transfer, proton transfer in the excited state, ring opening and closing mechanism. These isomerizations affect optical properties. For example, the absorption maximum of (Z)-azobenzene is blue shifted with respect to (E)-azobenzene. Many light-driven azo-based switches have been investigated.

Chiroptical Chiroptical molecular switches are a specific subgroup with photochemical switching taking place between enantiomers. In these compounds the "readout" is by circular dichroism. Hindered alkenes can change their helicity (see: planar chirality) as response to irradiation with right or left-handed circularly polarized light. Chiroptical molecular switches that show directional motion are considered synthetic molecular motors. When attached to the end of a helical poly (isocyanate) polymer, they can switch the helical sense of the polymer.

Redox active Species that exist in more than oneredox state are potential switches. When the optical properties of the redox state differ, then redox is sometimes called electrochromism. For instance, Ferrocene, which is orange, oxidizes to the blue ferrocenium cation. Many fluorescence based sensors are based on redox couple mechanism of switches which in their oxidized form quenches the fluorescence of fluorophore while in reduced state does not, or vice versa. Some other examples include, biindeno[2,1-b]thiophenylidene (BTP), viologens, napthelene diimides, bipyridinium, and metal-ligand redox complex.

… excerpt ends here. Continue reading the full article.

Illustrations

Molecular switch: Types of endogenous and exogenous stimuli for molecular switches.
Types of endogenous and exogenous stimuli for molecular switches.
Molecular switch: The dual responsive behavior of spiropyran
The dual responsive behavior of spiropyran
Molecular switch: pH responsive Hydrazone switches having potential for 19F MRI Contrast agent. Picture shows the structural change in the hydrazone molecule by acid or base.
pH responsive Hydrazone switches having potential for 19F MRI Contrast agent. Picture shows the structural change in the hydrazone molecule by acid or base.
Molecular switch: The sol-gel transition of acid sensitive amines using trichloroacetic acid (TCA)[24]
The sol-gel transition of acid sensitive amines using trichloroacetic acid (TCA)[24]
Molecular switch illustration

Worked examples

Example 1 — a first encounter with Molecular switch

Start with the simplest possible case. Write down what Molecular switch claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Molecular switch before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Molecular switch ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Molecular switch

In research
Molecular switch appears in chemistry research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Molecular switch in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Molecular switch is common in secondary-school and first-year university syllabi. It links to neighbouring topics Molecular machines, Supramolecular chemistry, so understanding it makes those chapters shorter.
In everyday life
Look for Molecular switch outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.

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How to study Molecular switch in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Molecular switch means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Molecular switch out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Molecular switch in simple terms?

A molecular switch is a molecule that can be switched between two or more stable or metastable states with the use of any external (exogenous) or internal (endogenous) stimuli, such as changes in pH, light, temperature, an electric current, a microenvironment, or in the presence of ions, and other…

Why does Molecular switch matter?

Because it connects several chemistry ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Molecular switch?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Molecular switch.

Tags

  • Molecular machines
  • Supramolecular chemistry

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