Atranes are a class of tricyclic
with three five-membered rings. It is a
heterocyclic structure similar to the
. It has a transannular
dative bond from a
nitrogen at one bridgehead to a
atom such as silicon or boron at the other bridgehead.
[Voronkov, Mikhail G.; Baryshok, Viktor P. "Atranes - a new generation of biologically active substances" (in Russian) Vestnik Rossiiskoi Akademii Nauk 2010, volume 80, 985-992.] The name "atrane" was first proposed by .
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Nomenclature
Various atranes are named depending on the central Chemical element, e.g. "silatrane" (E = silicon); "boratrane" (E = boron); "phosphatrane" (E = phosphorus), etc. It is also proposed that when Y = nitrogen, the prefix "aza" be inserted before element + "atrane" (azasilatrane, for example) because atranes wherein E = silicon and Y = oxygen have been referred to as just "silatranes".
Structure and properties
Silatranes exhibit unusual properties, as the transannular coordinate bond in atranes can be stretched (quasiatranes) and even broken (proatranes). The strength (and multiplicity) of the central bond depends on the stereoelectronic properties of the surrounding ligands, the electronegativity of the participating atoms, and the size of the rings. A strong driving force for the formation of the central bond is relief of ring strain from the otherwise-formed 8-membered rings.[
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Atranes exhibit biological activity in which the coordination of nitrogen to silane plays an important role. Some derivatives such as phenylsilatrane are highly toxic.
Proazaphosphatrane is a very strong non- base and is utilized in various types of Organic compound synthesis as an efficient catalyst.
See also
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Stannatrane
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Hypervalent molecule
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Scorpionate ligand
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Chinese lantern structure
