Fluorine-18 is a radioisotope of the chemical element fluorine, which, in addition to the element-specific 9 protons, has 9 neutrons in the atomic nucleus, resulting in the mass number 19. As a positron-emitting radionuclide, 18F is of practical importance in medical education (see below).
The radioactive isotope was first described in 1937: Fluorine-18 was observed during the irradiation of quartz and other solid oxides with protons (3.8 MeV) as a product of the nuclear reaction 18O (p,n)18F [1].
See also: list of Fluorine isotopes.
Half-life T½ = 109.734(8) min (minutes) respectively 6.58404 × 103 seconds s.
Decay mode | Daughter | Probability | Decay energy | Details | γ energy (intensity) |
---|---|---|---|---|---|
EC/β+ | 18O | 100 % | 1.6559(5) MeV | β+: 0.2498(3) MeV [96.73(4) %] | Annihilation: 0.5110 MeV [193.46(8) %] |
Direct parent isotope is: 18Ne.
Fluorine-18 can be produced artificially in nuclear reactors, but preferably in accelerators (cyclotrons and linear accelerators). Overall, there are a whole series of nuclear reactions that lead to 18F; these include:
- 18O(p,n)18F,
-16O(3He,p)18F,
- 16O(α,pn)18F,
- 20Ne(d,α)18F,
- 20Ne(p,2n)18F,
- 20Ne(3He,n)18Ne, which then naturally leads to
- 6Li(n,α)3H/16O(3H,n)18F.
Fluorine-18 for medical and research purposes is produced by cyclotron irradiation of the respective target molecules (often Water-18O).
A detailed and comprehensive overview of fluorine-18 radiochemistry, 18F labeling strategies and the synthesis routes to 18F-labeled molecules has been published by Orit Jacobsen et al. in an open-access article [4].
Fluorine-18 only occurs in small traces in nature. The main sources here are the spallation by cosmic radiation of atmospheric argon and the reaction of protons with natural oxygen-18.
Fluorine-18 is an important source of positrons in medicine. Radiopharmaceuticals labelled with 18F are used in particular in positron emission tomography (18F-PET), an imaging technique that detects the positrons emitted by the radioactive decay of the isotope and processes them into an image that is used for diagnostic purposes.
(Chemical) data sheets are available here for the following radioactive 18F tracers:
- Florbenazine (18F) (experimental),
- Florbenguane (experimental).
Nuclear isomers or excited states with the activation energy in keV related to the ground state.
Nuclear Isomer | Excitation Energy | Half-life | Spin |
---|---|---|---|
18mF | 1121.36(15) keV | 162(7) ns | 5+ |
Z | Isotone N = 9 | Isobar A = 18 |
---|---|---|
3 | 12Li | |
4 | 13Be | |
5 | 14B | 18B |
6 | 15C | 18C |
7 | 16N | 18N |
8 | 17O | 18O |
9 | 18F | 18F |
10 | 19Ne | 18Ne |
11 | 20Na | 18Na |
12 | 21Mg | 18Mg |
13 | 22Al | |
14 | 23Si | |
15 | 24P |
[1] - L. A. DuBridge, S. W. Barnes, J. H. Buck:
Proton Induced Radioactivity in Oxygen.
In: Physical Review, 51, 995, (1937), DOI 10.1103/PhysRev.51.995.
[2] - Erin L. Cole et al.:
Radiosyntheses using Fluorine-18: The Art and Science of Late Stage Fluorination.
In: Current Topics in Medicinal Chemistry, 14, 7, (2014), DOI 10.2174/1568026614666140202205035.
[3] - Kaiqiang Zhang, Wanru Feng, Zhaobiao Mou, Jiayin Chen, Xiaoqun Tang, Prof. Dr. Zijing Li:
18F-Labeling Chemistry in Aqueous Media.
In: Chemistry - A European Journal, 29, 37, (2023), DOI 10.1002/chem.202300248.
[4] - Orit Jacobson, Dale O. Kiesewetter, Xiaoyuan Chen:
Fluorine-18 Radiochemistry, Labeling Strategies and Synthetic Routes.
In: Bioconjugate Chemistry, 26, 1, 1–18, (2014), DOI 10.1021/bc500475e.
Last update: 2024-10-19
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