Examples of 'diborane' in a sentence
Meaning of "diborane"
diborane (noun) - a chemical compound consisting of boron and hydrogen atoms, with the formula B2H6, known for its highly reactive and flammable nature
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- boron hydride, B₂H₆, a colourless explosive gas with a nasty smell; it has an unusual structure in which two of the hydrogen atoms form a bridge between the two boron atoms
How to use "diborane" in a sentence
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diborane
Excess diborane was destroyed by careful addition of MeOH.
It is much more stable in presence of water than diborane.
Excess diborane was destroyed by the addition of water.
G designates the percentage of diborane in the first mixture.
Diborane is a key boron compound with a variety of applications.
The preferred reducing agent is diborane.
Diborane and decaborane and their derivates were also investigated.
Reduction may also be carried out by means of diborane.
Diborane is one of many compounds with such unusual bonding.
A preferred reducing reagent is diborane tetrahydrofuran.
Diborane can also be used.
Most preferred as reducing agents are borane and diborane.
Extensive studies of diborane have led to the development of multiple syntheses.
Diglyme is also used as a solvent in hydroboration reactions with diborane.
Lithium aluminum hydride and diborane are used as the reducing agent.
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The reduction may be accomplished using a borane or diborane as well.
Diborane is a highly reactive and versatile reagent that has numerous applications.
Water was added dropwise to the solution to decompose excess diborane.
Diborane is so central and has been studied so often that many syntheses exist.
This type of bonding occurs in electron deficient compounds like diborane.
Diborane is used as a reducing agent roughly complementary to the reactivity of lithium aluminium hydride.
This is an important intermediate in the pyrolosis of diborane to produce higher boranes.
Obtained diborane and ammonia products can become the synthesis precursors enabling the full recyclability.
Typical reducing agents include the alkali metal borohydrides and diborane.
Unlike diborane however, most organoboranes do not form dimers.
Products of the hydride reduction are isolated as a borane complex when diborane is used.
Diborane can be used in order to obtain p-doped silicon nanowires.
The total hydrogen in the gas mixture includes the hydrogen used to dilute the diborane.
Similar, a chemisorption of diborane alters the sorption characteristics of zeolites.
He proposed the first ethane-like structure of diborane.
Now, diborane and phosphine are extremely dangerous gases in high concentration.
Structure of Diborane.
Diborane increases the growth rate, but arsine and phosphine decrease it.
As an example of the reducing agent, diborane may be cited.
Upon completion of the diborane addition, the reactor solution was allowed to stir overnight.
Process for supplying a gas, especially of diborane and silane.
It is typical to use B2H6 diborane gas to diffuse boron into the silicon material.
In this fourth preferred embodiment, the reducing agent is diborane.
Examples of suitable reducing agents include diboranes, such as diborane or diborane-dimethyl sulphide complex.
In this first preferred embodiment, the reducing agent is diborane.
Suitable hydride reducing agents include lithium aluminum hydride, diborane, and lithium borohydride, preferably diborane.
In the absence of other chemical species, it reacts with itself to form diborane.
The maximum filling density for Diborane shall not exceed 7 percent.
Suitable reducing agents include lithium aluminum hydride, lithium borohydride, and diborane.
Diborane is the chemical compound consisting of boron and hydrogen with the formula B2H6.
Thus, this doping may be a P-type doping using a boron precursor such as diborane.
Diborane adopts a D2h structure containing four terminal and two bridging hydrogen atoms.
Shortly after, experimental spectroscopic work was performed by Price that confirmed Longuet-Higgins ' structure for diborane.
Reduction of the diketopiperazine XXXVII with diborane can afford the N-benzyl protected version of compound V.
Reduction of 3-fluorophenylacetic acid vía diborane reduction.
