We prefer to identify with small, easily isolable fractions of the total culture.

Since this is an 18-electron complex, it is expected to be isolable compound.

Curium is one of the most radioactive isolable elements.

A mind is not an isolable object.

Sulfurous acid is not an isolable compound and does not appear to exist in solution either.

The few isolable hemithioacetals are all cyclic, which disfavors dissociation.

Another class of isolable hemithioacetals are derived from carbonyl groups that form stable hydrates.

Like many strong acids, hexafluorophosphoric acid is not isolable but is handled only in solution.

Another isolable hemithioacetal can be prepared by addition of thiol to methyl glyoxalate.

Although vanadium phosphinimides are isolable, they are not very highly active catalysts.

The first isolable dialkylgermylene was synthesised in 1991:

It is a rare isolable homoleptic metal carbonyl that is paramagnetic.

Abbreviated t-BuCP, it was the first example of an isolable phosphaalkyne.

Dinitrogen trioxide is only isolable at low temperatures, i.e. in the liquid and solid phases.

In the main group elements, sulfur, xenon, selenium, and tellurium form isolable hexafluorides.

Chlorine is the only halogen to form an isolable acid of formula HXO.

In general, organocerium compounds are not isolable, and are rather studied in solution via their reactions with other species.

Disilenes bearing sterically bulky substituents are isolable and have been well characterized although they remain mainly of academic interest.

There are other related acids with the general formula HO (SO) though none are isolable.

Precipitation of sodium chloride thus drives the formation of the oxonium acid compound, which is isolable as a solid.

Additionally, it is the only known anion capable of forming a stable, isolable salt with protonated benzene, CH.

The major base is N-methyltetrahydroharman, isolable to 0.3%, but there are also trace amounts of tetrahydroharman and N-methyl tetrahydroharman.

This would be a fortunate state of affairs since the existence of simple and isolable subsystems is thought to be a precondition for successful science .

When diazoethane is substituted for diazomethane, a hydride shift produces the ketone (XII), the only isolable product.

For example, an acyl-diazomethane can react with an aldehyde in the presence of a DBU catalyst to form isolable α-diazo-β-hydroxy esters (shown below).