Methylboranes are formed by the reaction of diborane and trimethylborane. This reaction produces four different substitution of methyl with hydrogen on diborane. Produced is 1-methyldiborane, 1,1-dimethyldborane, 1,1,2-trimethyldiborane and 1,1,2,2-tetramethyldiborane. The reaction is complex. At 0 °C when diborane is in excess, monomethyldiborane is initially produced, coming to a steady but low level, and 1,1-dimethyldiborane level increases over a long time, until all trimethylborane is consumed. Monomethyldiborane ends up at equilibrium with a mixture of diborane and dimethyldiborane. At 0° the equilibrium constant for 2B2H5Me ←→ B2H6 + (BH2Me)2 is around 0.07, so monomethyldiborane will typically be the majority of the mixture, but there will still be a significant amount of diborane and dimethyldiborane present. Monomethyldiborane yield is best with a ratio of 4 of diborane to 1 of trimethylborane. The yield of trimethyldiborane is maximised with ratio of 1 of diborane to 3 of trimethylborane.
When methyllithium reacts with diborane, monomethyldiborane is produced in about a 20% yield.
Tetramethyl lead can react with diborane in a 1,2-dimethoxyethane solvent at room temperature to make a range of methyl substituted diboranes, ending up at trimethylborane, but including 1,1-di, tridiborane. The other outputs of the reaction are hydrogen gas and lead metal.
Other methods to form methyldiboranes include reacting hydrogen with trimethylborane between 80 and 200 °C under pressure, or reacting a metal borohydride with trimethylborane in the presence of hydrogen chloride, aluminium chloride or boron trichloride. If the borohydride is sodium borohydride, then methane is a side product. If the metal is lithium then no methane is produced. dimethylchloroborane and methyldichloroborane are also produced as gaseous products.
When Cp2Zr(CH3)2 reacts with borane dissolved in tetrahydrofuran, a borohydro group inserts into the zirconium carbon bond, and methyl diboranes are produced.
When trimethylgallium reacts with diborane at -45°, methyldiborane is produced along with dimethylgallium borohydride.
The compound boils at −43 °C.
Methyldiborane liquid has a density of 0.546 g/ml at −126° At −78.5 the vapour pressure is 55 torr.
Methyldiborane HCH3BH2BH2 has one methyl group and a hydrogen on a boron atom. The other boron atom is only bound to hydrogen atoms. A bridge of two hydrogen atoms links the boron atoms together. The methyldiborane molecule has the following measurements: B1 is the boron atom not attached to the methyl group and B2 is the boron atom that has methyl group attached, and Hμ is one of the bridge hydrogen atoms between the boron atoms. The distance between boron atoms is 1.82 Å, Distance between boron atoms and bridging hydrogen atoms is 1.34 Å. Distances to non bridging hydrogens from B1 are 1.195 and 1.187 Å. B2 distance to non bridging hydrogen is 1.2 Å. Distance between two bridging hydrogen atoms is 1.96 Å. The carbon to boron bond is 1.49 Å long. The angle subtended from the bridging hydrogens to the boron to boron axis is 47°. The angle of carbon to the boron-boron axis is 120°. The dipole moment of methyldiborane is 0.56 D. It has a vapour pressure of 61 mm Hg at −77.2 °C. The predicted heat of formation for the liquid is ΔH0f=−14 kcal/mol, and for the gas −9 kcal/mol.
A gas chromatograph can be used to determine the amounts of the methyl boranes in a mixture. The order they pass through are diborane, monomethyldiborane, trimethylborane, 1,1-dimethyldiborane, 1,2-dimethyldiborane, trimethyldiborane, and last tetramethyldiborane.
The nuclear resonance shift for the bridge hydrogen is 10.09 ppm, compared to 10.49 for diborane.
At -78.5 °C methyldiborane disproportionates slowly first to diborane and 1,1-dimethyldiborane. In solution methylborane is more stable against disproportionation than dimethylborane.
By reacting methyldiborane with ether, dimethylether borine is formed (CH3)2O.BH3 leaving methylborane which rapidly dimerises to 1,2-dimethyldiborane.
Methyldiborane is hydrolyzed in water to methylboronic acid CH3B(OH)2.
Methyldiborane reacts with trimethylamine to yield solid derivatives trimethylamine-methylborane (CH3)3N—BHCH3 and trimethylamine-borane (CH3)3N—BH3.
Methyldiborane is pyrophoric, spontaneously inflaming when exposed to air.
When methyldiborane is oxidised around 150 °C a substance 2-methyl-1,3,4-trioxadiboralane is produced. This is a ring of three oxygen atoms and two boron atoms, with methyl attached to one boron atom. At the same time dimethyltrioxadiboralane and trimethylboroxine are also formed, and also hydrocarbons, diborane, hydrogen, and dimethoxyborane (dimethyl methylboronic ester).
When methyldiborane, or dimethyldiborane is combined with ammonia, aminodimethylborine (NH2B2) is formed and on heating around 180 °C B-methyl borazoles are produced. These borazoles can have zero, one, two or three methyl groups substituted on the boron atoms (B3N3H6, MeB3N3H5, Me2B3N3H4 or Me3B3N3H3).
A specific way to make 1,2-dimethyldiborane is to react methyldiborane with a sufficient amount of a Lewis base. This will strip off borane to combine with the Lewis base, and let two methyl borane molecules dimerise.
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