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Organic superbases are mostly charge-neutral, nitrogen containing species, where nitrogen act as a proton acceptor. These include the phosphazenes, phosphanes , amidines, and guanidines. Other organic compounds that meet the physicochemical or structural definitions of 'superbase' include proton chelators like the aromatic proton sponges and ...
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This page was last edited on 21 February 2021, at 05:54 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Well known phosphazene bases are BEMP (2-tert-Butylimino-2-diEthylamino-1,3-diMethylperhydro-1,3,2-diazaPhosphorine) with an acetonitrile pK a of the conjugate acid of 27.6 and the phosphorimidic triamide t-Bu-P 4 (pK BH + = 42.7) also known as Schwesinger base. [2]
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