Synthesis\nof Aminodiborane through the Reaction of\nAmmonia Borane with Acids

A facile\nmethod for the synthesis of aminodiborane (NH<sub>2</sub>B<sub>2</sub>H<sub>5</sub>, ADB) has been developed through\nthe reaction\nof ammonia borane (NH<sub>3</sub>BH<sub>3</sub>, AB) with an ether\nsolution of hydrogen chloride (HCl·Et<sub>2</sub>O) at room temperature.\nIn addition, <i>N</i>-alkyl substituted ADB derivatives\nwere synthesized by reacting <i>N</i>-alkyl substituted\nAB with HCl·Et<sub>2</sub>O at 50 °C. The mechanistic studies\nindicated that the nucleophilic substitution reaction of the B–H\nbonding pair electrons and the dihydrogen bonding interaction play\nan important role. This work paves an alternative way to prepare amine\nborane compounds.

Publication Details

Journal
Figshare
Published
2024-11-04
DOI
https://doi.org/10.1021/acs.inorgchem.4c03522.s001
Primary Topic
Organoboron and organosilicon chemistry
Type
article
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article

Synthesis\nof Aminodiborane through the Reaction of\nAmmonia Borane with Acids

Figshare
Organoboron and organosilicon chemistry
article

Synthesis\nof Aminodiborane through the Reaction of\nAmmonia Borane with Acids

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Abstract

A facile\nmethod for the synthesis of aminodiborane (NH<sub>2</sub>B<sub>2</sub>H<sub>5</sub>, ADB) has been developed through\nthe reaction\nof ammonia borane (NH<sub>3</sub>BH<sub>3</sub>, AB) with an ether\nsolution of hydrogen chloride (HCl·Et<sub>2</sub>O) at room temperature.\nIn addition, <i>N</i>-alkyl substituted ADB derivatives\nwere synthesized by reacting <i>N</i>-alkyl substituted\nAB with HCl·Et<sub>2</sub>O at 50 °C. The mechanistic studies\nindicated that the nucleophilic substitution reaction of the B–H\nbonding pair electrons and the dihydrogen bonding interaction play\nan important role. This work paves an alternative way to prepare amine\nborane compounds.

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Organoboron and organosilicon chemistry
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