silane

I'm not too concerned about your getting hold of silane.

Silane is of practical interest as a precursor to silicon metal.

By replacing the alcohol with a silane, C-glycosides can be formed.

A coupling agent such as silane is used to enhance the bond between these two components.

Like the related compounds silane and methane, germane is tetrahedral.

It is an intermediate between silane and silicon tetrachloride.

Therefore, silane is commonly used to create a thin tungsten nucleation layer.

There are many structural analogues of silane, which do not necessarily contain an organic functional group.

These rules are almost the same as those of alcohol, with the exception that silane is used as the mother hydride.

Infrared spectroscopy may also be useful as it can indicate whether or not the product is a tertiary silane.

Triethylsilane can be prepared by the reaction between three equivalents of ethylene and silane.

Other engines use pyrophoric fuel additives, such as silane, to avoid such issues.

Silane is slightly heavier than air (possibility of pooling at ground levels/pits)

Industrially, silane is produced from metallurgical grade silicon in a two-step process.

Several industrial and medical applications exist for silane and functionalized silanes.

Dr. Silane looked at him in disbelief, and answered, "Isn't that fabulous."

It uses as source material either laser ablated particles or a feed gas such as silane.

It is a derivative of silane.

Silane is the silicon analogue of methane.

In general, ormosils are produced by adding silane to silica-derived gel during the sol-gel process.

This reaction produces silane, disilane, and even trisilane.

The method has been abandoned for the production of silane, but it remains viable for generating disilane.

The parent compound SiH is called silane, and an example is phenylsilane.

One method used to overcome this problem is to convert it to a less reactive bis(dimethylamino)silane.

Silane is an inorganic compound with chemical formula SiH.