Issue 4, 1981

Synthesis of [18F]XeF2, a novel agent for the preparation of 18F-radiopharmaceuticals

Abstract

[18F]XeF2 was synthesised by isotopic exchange between XeF2 and anhydrous reactor-produced [18F]HF, [18F]SiF4, and [18F]AsF5 with a radiochemical yield of 30%; [18F]XeF2 may facilitate the direct radiofluorination of organic tracer molecules for positron emission tomography.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 198-199

Synthesis of [18F]XeF2, a novel agent for the preparation of 18F-radiopharmaceuticals

G. S. G. Firnau, R. Chirakal and E. S. Garnett, J. Chem. Soc., Chem. Commun., 1981, 198 DOI: 10.1039/C39810000198

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements