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Updated: Sep 29, 2025

Characterizing Lewis Pairs Using Titration Coupled with In Situ Infrared Spectroscopy
Published on: February 20, 2020
Frustrated Lewis pair chemistry of hydride sponges
Christian Becker1, Jan Schwabedissen1, Beate Neumann1
1Lehrstuhl für Anorganische Chemie und Strukturchemie, Fakultät für Chemie, Universität Bielefeld, Universitätsstraße 25, 33615 Bielefeld, Germany. mitzel@uni-bielefeld.de.
Abstract:
An improved synthesis for 1,8-bis(dimethylboranyl)naphthalene (1, hydride sponge) was developed avoiding the use of tin(IV) reagents. The related 1,2-bis(dimethylboranyl)benzene (2) was prepared. 1 combined with 1,8-bis(dimethylamino)naphthalene (3, proton sponge) is a Frustrated Lewis pair (FLP) that forms adducts [1-EH][3-H] with the protic compounds EH = H2O, NH3, H2S, PH3, H2Se, HCN. Their structures show the chelation of the deprotonated substrates, except for CN- (binds to one B atom of 1). The mechanisms of formation of [1-EH][3-H] were explored by NMR spectroscopy. Similar reactions took places for the FLP system 2 + 3, but the adducts [2-EH][3-H] are less stable; only the PH3 adduct was isolated and AsH3 forms a chelated adduct [2-NC(CD3)AsH2][3-H]. FLP 1 + 3 does not react with molecular hydrogen, but the formal adduct [1-H][3-H] was isolated via salt metathesis from K[1-H] and [3-H]Cl; it is stable towards water, atmospheric oxygen and up to 100 °C; its thermal decomposition proceeds without formation of H2. The stabilities of both, the mixture 1 + 3 + H2 and the formal adduct [1-H][3-H], allow concluding that hydrogen activation of FLP 1 + 3 is kinetically prevented.
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