Information about Chemiluminescence
A chemoluminescent reaction carried out in an erlenmeyer flask producing a large amount of light.
- [A] + [B] → [◊] → [Products] + light
For example, if [A] is luminol and [B] is hydrogen peroxide in the presence of a suitable catalyst we have:
- luminol + H2O2 → 3-APA[◊] → 3-APA + light
where:
- where 3-APA is 3-aminophthalate
- 3-APA[◊] is the excited state fluorescing as it decays to a lower energy level.
A standard example of chemiluminescence in the laboratory setting is found in the luminol test, where evidence of blood is taken when the sample glows upon contact with iron. When chemiluminescence takes place in living organisms, the phenomenon is called bioluminescence. A lightstick emits light by chemiluminescence.
Liquid-phase reactions
- Luminol in an alkaline solution with hydrogen peroxide in the presence of iron or copper[1], or an auxiliary oxidant[2], produces chemiluminescence. The luminol reaction is
- luminol + H2O2 → 3-APA[◊] → 3-APA + light
- Cyalume®, as used in a lightstick, emits light by chemiluminescence of a fluorescent dye (also called sensitiser) activated by cyalume reacting with hydrogen peroxide in the most efficient non-enzymatic reaction known.[3]
- cyalume + H2O2 + dye → phenol + 2CO2 + dye[◊]
When the activated fluorescent dye decays to a lower energy level, light is given off. The color depends upon the dye.[4].
| Color | Sensitiser |
|---|---|
| Blue | 9,10-Diphenylanthracene |
| Green | 9,10-Bis(phenylethynyl)anthracene |
| Yellow-green | Tetracene |
| Yellow | 1-Chloro-9,10-bis(phenylethynyl)anthracene |
| Orange | 5,12-Bis(phenylethynyl)-naphthacene, Rubrene, Rhodamine 6G |
| Red | Rhodamine B |
- Oxalyl chloride (C2O2Cl2) produces light when oxidized - but only in the presence of a sensitiser, similar to the above examples. If oxalyl chloride is treated with H2O2 in non-aqueous media (e.g. CH2Cl2) in the presence of a sensitiser, emission of light is obtained. The colour, intensity and duration of light emission depend on the sensitiser used. Rodamin 6 G gives bright orange light with moderate duration of emission.
- Ru(bipy)32+ is a ruthenium(II) complex which undergoes oxidation to ruthenium(III) if certain oxidizing agents are introduced. If ruthenium(III) complex is then reduced in alkaline medium, emission of light occurs. First, there is a reaction:
- 2Ru(bipy)32+ + PbO2 + 4H+ → 2Ru(bipy)33+ + Pb2+ + 2H2O
- Here, Ru(III) is obtained. Further reaction includes use of solution of sodium tetrahydroborate(III), NaBH4 in alkaline medium. When the solution is added, Ru(III) is reduced to Ru(II) an orange light is emitted.
- TMAE (tetrakis(dimethylamino)ethylene) emits clear blue-green light upon oxidation by air.
- Pyrogallol (1,2,3-trihydroxibenzene) is also capable of light emission. If an aqueous solution of pyrogallol, NaOH and K2CO3 is mixed with formaldehyde, short-lived red emission occurs.
- Pure oxygen (O2) can also emit light. If solutions of 30% hydrogen peroxide and 5% alkaline sodium hypochlorite (NaClO) are mixed, red light is emitted. It is barely visible, though - for this reason, in such experiment sensitiser is often included to boost light emission in terms of brightness and intensity. Again, both colour and intensity of light depend on sensitiser used.
- Lucigenin oxidation is also very well known among chemiluminescence reactions. If an aqueous lucigenin solution is mixed with highly alkaline aqueous solution containing ethanol or acetone and hydrogen peroxide, very bright green emission is produced that decays to greenish blue and finally blue emission. The duration of the emission can be up to a couple of minutes under the right circumstances. [5].
- Solutions containing ions of manganese (VII, IV, III) show Chemiluminescence (690 nm) when reduced by sodium borohydride at low pH to Mn(II) [6]
Gas-phase reactions
- One of the oldest known chemoluminescent reactions is that of elemental white phosphorus oxidizing in moist air, producing a green glow. This is actually a gas-phase reaction of phosphorus vapor, above the solid, with oxygen producing the excited states (PO)2 and HPO.[6]
- Another gas phase reaction is the basis of nitric oxide detection in commercial analytic instruments applied to environmental air quality testing. Ozone is combined with nitric oxide to form nitrogen dioxide in an activated state.
- NO+O3 → NO2[◊]+ O2
- The activated NO2[◊] luminesces broadband visible to infrared light as it reverts to a lower energy state. A photomultiplier and associated electronics counts the photons which are proportional to the amount of NO present. To determine the amount of nitrogen dioxide, NO2, in a sample (containing no NO) it must first be converted to nitric oxide, NO, by passing the sample through a converter before the above ozone activation reaction is applied. The ozone reaction produces a photon count proportional to NO which is proportional to NO2 before it was converted to NO. In the case of a mixed sample containing both NO and NO2, the above reaction yields the amount of NO and NO2 combined in the air sample, assuming that the sample is passed through the converter. If the mixed sample is not passed through the converter, the ozone reaction produces activated NO2[◊] only in proportion to the NO in the sample. The NO2 in the sample is not activated by the ozone reaction. Though unactivated NO2 is present with the activated NO2[◊], photons are only emitted by the activated species which is proportional to original NO. Final step, subtract NO from (NO + NO2) to yield NO2
Bioluminescence
The firefly reaction has the highest known quantum efficiency, QC of 88%, for chemiluminescence reactions. ATP (adenosine tri-phosphate), the ubiquitous biological energy source, reacts with luciferin with the aid of the enzyme luciferase to yield an intermediate complex. This complex combines with oxygen to produce a highly chemiluminescent compound.
ECL
Enhanced chemiluminescence (ECL) is a common technique for a variety of detection assays in biology. A horseradish peroxidase enzyme (HRP) is tethered to the molecule of interest (usually through labeling an immunoglobulin that specifically recognizes the molecule). This enzyme complex, then catalyzes the conversion of the ECL substrate into a sensitized reagent in the vicinity of the molecule of interest, which on further oxidation by hydrogen peroxide, produces a triplet (excited) carbonyl which emits light when it decays to the singlet carbonyl. Enhanced chemiluminescence allows detection of minute quantities of a biomolecule. Proteins can be detected down to femtomole quantities (ECL review), well below the detection limit for most assay systems.The mechanism of action for a typical ECL reagent:
Applications
- gas analysis: for determining small amounts of impurities or poisons in air. Other compounds can also be determined by this method (ozone, N-oxides, S-compounds). Typical example is NO determination with detection limits down to 1 ppb
- analysis of inorganic species in liquid phase
- analysis of organic species: useful with enzymes, where the substrate isn't directly involved in chemiluminescence reaction, but the product is
- detection and quantitation of biomolecules in assay systems such as ELISA and Western blots
- DNA sequencing using pyrosequencing
External links and references
1. ^ Luminol chemistry laboratory demonstration. Retrieved on 2006-03-29.
2. ^ Investigating luminol (PDF). Salters Advanced Chemistry. Retrieved on 2006-03-29.
3. ^ Rauhut, Michael M. (1985), Chemiluminescence. In Grayson, Martin (Ed) (1985). Kirk-Othmer Concise Encyclopedia of Chemical Technology (3rd ed), pp 247 John Wiley and Sons. ISBN 0-471-51700-3
4. ^ Helmenstine, Anne Marie (Aug 10, 2004). Light stick chemistry, retrieved Sept. 22, 2004.
5. ^ For more information about how to perform experiments mentioned, see the reference Bassam Z. Shakhashiri: Chemical Demonstrations, Volume 1, University of Wisconsin 1983.
6. ^ New light from an old reagent: Chemiluminescence from the reaction of potassium permanganate with sodium borohydride. Neil W. Barnett, Benjamin J. Hindson , Phil Jones, Claire E. Lenehan and Richard A. Russell. Aust. J. Ed. Chem., 2005, 65,
2. ^ Investigating luminol (PDF). Salters Advanced Chemistry. Retrieved on 2006-03-29.
3. ^ Rauhut, Michael M. (1985), Chemiluminescence. In Grayson, Martin (Ed) (1985). Kirk-Othmer Concise Encyclopedia of Chemical Technology (3rd ed), pp 247 John Wiley and Sons. ISBN 0-471-51700-3
4. ^ Helmenstine, Anne Marie (Aug 10, 2004). Light stick chemistry, retrieved Sept. 22, 2004.
5. ^ For more information about how to perform experiments mentioned, see the reference Bassam Z. Shakhashiri: Chemical Demonstrations, Volume 1, University of Wisconsin 1983.
6. ^ New light from an old reagent: Chemiluminescence from the reaction of potassium permanganate with sodium borohydride. Neil W. Barnett, Benjamin J. Hindson , Phil Jones, Claire E. Lenehan and Richard A. Russell. Aust. J. Ed. Chem., 2005, 65,
| Lighting and Lamps | ||
|---|---|---|
| Incandescent: | Conventional - Halogen - Parabolic aluminized reflector (PAR) | |
| Fluorescent: | Compact fluorescent (CFL) - Linear fluorescent - Induction lamp | |
| Gas discharge: | High-intensity discharge (HID) - Mercury-vapor - Metal-halide - Neon - Sodium vapor | |
| Electric arc: | Arc lamp - HMI - Xenon arc - Yablochkov candle | |
| Combustion: | Acetylene/Carbide - Candle - Gas lighting - Kerosene lamp - Limelight - Oil lamp - Safety lamp | |
| Other types: | Sulfur lamp - Light-emitting diode (LED) - Fiber optics - Plasma | |
Light is electromagnetic radiation of a wavelength that is visible to the eye (visible light). In a scientific context, the word "light" is sometimes used to refer to the entire electromagnetic spectrum.
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- Luminescence is also the title of an album by singer Anggun.
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A reactant or reagent is a substance consumed during a chemical reaction.[1] Solvents and catalysts, although they are involved in the reaction, are usually not referred to as reactants.
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The IUPAC Gold Book[1] defines a reaction intermediate or an intermediate as a molecular entity (atom, ion, molecule...) with a lifetime appreciably longer than a molecular vibration (corresponding to a local potential energy minimum of depth greater than RT; R
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Light is electromagnetic radiation of a wavelength that is visible to the eye (visible light). In a scientific context, the word "light" is sometimes used to refer to the entire electromagnetic spectrum.
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Luminol is a versatile chemical that exhibits chemiluminescence, with a striking blue glow, when mixed with an appropriate oxidizing agent. It is a white to slightly yellow crystalline solid that is soluble in water and most polar organic solvents.
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The Avogadro constant (symbols: L, NA), also called the Avogadro number is the number of "entities" (usually, atoms or molecules) in one mole,[1][2] that is the number of carbon-12 atoms in 12 grams (0.
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Quantum efficiency (QE) is a quantity defined for a photosensitive device such as photographic film or a charge-coupled device (CCD) as the percentage of photons hitting the photoreactive surface that will produce an electron–hole pair.
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Luminol is a versatile chemical that exhibits chemiluminescence, with a striking blue glow, when mixed with an appropriate oxidizing agent. It is a white to slightly yellow crystalline solid that is soluble in water and most polar organic solvents.
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Blood is a specialized biological fluid consisting of red blood cells (also called RBCs or erythrocytes), white blood cells (also called leukocytes) and platelets (also called thrombocytes) suspended in a complex fluid medium known as blood plasma.
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- Luminescence is also the title of an album by singer Anggun.
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3, 4, 6
(amphoteric oxide)
Electronegativity 1.83 (Pauling scale)
Ionization energies
(more) 1st: 762.5 kJmol−1
2nd: 1561.9 kJmol−1
3rd: 2957 kJmol−1
Atomic radius 140 pm
Atomic radius (calc.
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(amphoteric oxide)
Electronegativity 1.83 (Pauling scale)
Ionization energies
(more) 1st: 762.5 kJmol−1
2nd: 1561.9 kJmol−1
3rd: 2957 kJmol−1
Atomic radius 140 pm
Atomic radius (calc.
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Bioluminescence is the production and emission of light by a living organism as the result of a chemical reaction during which chemical energy is converted to light energy.
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glowstick or lightstick is a translucent plastic tube which contains chemical substances capable of producing light through a chemical reaction induced chemoluminescence which does not require an electrical power source.
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Luminol is a versatile chemical that exhibits chemiluminescence, with a striking blue glow, when mixed with an appropriate oxidizing agent. It is a white to slightly yellow crystalline solid that is soluble in water and most polar organic solvents.
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Hydrogen peroxide (H2O2) is a very pale blue liquid which appears colourless in a dilute solution, slightly more viscous than water. It is a weak acid.
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Diphenyl oxalate (trademark name Cyalume) is a liquid ester whose oxidation products are responsible for the chemiluminescence in a glowstick.[1] It can be synthesized by fully esterifying phenol with oxalic acid.
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- For the '"Sensitiser" used in explosives see explosive.
A sensitiser in chemoluminescence is a chemical compound, capable of light emission after it has received energy from a molecule, which became excited previously in the chemical reaction.
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Diphenyl oxalate (trademark name Cyalume) is a liquid ester whose oxidation products are responsible for the chemiluminescence in a glowstick.[1] It can be synthesized by fully esterifying phenol with oxalic acid.
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Hydrogen peroxide (H2O2) is a very pale blue liquid which appears colourless in a dilute solution, slightly more viscous than water. It is a weak acid.
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9,10-Diphenylanthracene is a polycyclic aromatic hydrocarbon. It has the appearance of a slightly yellow powder. 9,10-Diphenylanthracene is used as a sensitiser in chemoluminescence. In lightsticks it is used to produce blue light.
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9,10-Bis(phenylethynyl)anthracene (BPEA) is an aromatic hydrocarbon with the chemical formula is C30H18. It displays strong fluorescence and is used as a chemiluminescent fluorophore with high quantum efficiency.
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- ''For the initiating explosive, see tetrazene.
Tetracene, also called naphthacene, benz[b]anthracene and 2,3-benzanthracene, is a polycyclic aromatic hydrocarbon. It has the appearance of a pale yellow powder.
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1-Chloro-9,10-bis(phenylethynyl)anthracene is a fluorescent dye used in lightsticks. It emits yellow-green light, used in 30-minute high-intensity Cyalume sticks.
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See also
- 9,10-Bis(phenylethynyl)anthracene
- 2-Chloro-9,10-bis(phenylethynyl)anthracene
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Rubrene (5,6,11,12-tetraphenylnaphthacene) is a red colored polycyclic aromatic hydrocarbon. It has the appearance of a red crystalline powder.
Rubrene is used as a sensitiser in chemoluminescence. In lightsticks it is used to produce yellow light.
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Rubrene is used as a sensitiser in chemoluminescence. In lightsticks it is used to produce yellow light.
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Rhodamine (IPA: /ˈroʊdəmiːn/) is a family of related chemical compounds, fluorone dyes. Examples are Rhodamine 6G and Rhodamine B. They are used as a dye and as a dye laser gain medium.
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Rhodamine (IPA: /ˈroʊdəmiːn/) is a family of related chemical compounds, fluorone dyes. Examples are Rhodamine 6G and Rhodamine B. They are used as a dye and as a dye laser gain medium.
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Oxalyl chloride is a chemical compound with the formula (COCl)2. This colourless liquid, the diacid chloride of oxalic acid, is a useful reagent in organic synthesis.[1] It can be prepared by treating oxalic acid with phosphorus pentachloride.
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Ruthenium(II) tris(bipyridine) dichloride is the chemical compound with the formula [Ru(bipy)3]Cl2. This salt is obtained as the hexahydrate, although all of the properties of interest are in the cation [Ru(bipy)3]2+
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4, 6, 8
(mildly acidic oxide)
Electronegativity 2.2 (scale Pauling)
Ionization energies 1st: 710.2 kJ/mol
2nd: 1620 kJ/mol
3rd: 2747 kJ/mol
Atomic radius 130 pm
Atomic radius (calc.
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(mildly acidic oxide)
Electronegativity 2.2 (scale Pauling)
Ionization energies 1st: 710.2 kJ/mol
2nd: 1620 kJ/mol
3rd: 2747 kJ/mol
Atomic radius 130 pm
Atomic radius (calc.
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