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Astatine is known to bind to boron, [62] carbon, and nitrogen. [63] Various boron cage compounds have been prepared with At–B bonds, these being more stable than At–C bonds. [64] Astatine can replace a hydrogen atom in benzene to form astatobenzene C 6 H 5 At; this may be oxidized to C 6 H 5 AtCl 2 by chlorine.
Astatine can replace a hydrogen atom in benzene to form astatobenzene C 6 H 5 At; this may be oxidized to C 6 H 5 AtCl 2 by chlorine. By treating this compound with an alkaline solution of hypochlorite, C 6 H 5 AtO 2 can be produced. [31] Astatine-labelled iodine reagents have been used to synthesise RAt, RAtCl 2, R 2 AtCl, and RAtO 2 (R ...
Two-step procedures are used today, first synthesising stable astatoaryl prosthetic groups before incorporating them into the protein. [3] Not only is the C–At bond the weakest of all carbon–halogen bonds (following periodic trends), but also the bond easily breaks as the astatine is oxidised back to free astatine.
Astatine has 23 nuclear isomers (nuclei with one or more nucleons – protons or neutrons – in an excited state). A nuclear isomer may also be called a " meta -state"; this means the system has more internal energy than the " ground state " (the state with the lowest possible internal energy), making the former likely to decay into the latter.
In chemistry, an interhalogen compound is a molecule which contains two or more different halogen atoms (fluorine, chlorine, bromine, iodine, or astatine) and no atoms of elements from any other group. Most interhalogen compounds known are binary (composed of only two distinct elements).
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Astatine-229 This page was last edited on 23 January 2021, at 05:47 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 License ...
This page was last edited on 12 November 2022, at 21:48 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.