Potassium bis(trimethylsilyl)amide

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

<templatestyles src="Chembox/styles.css"/>

Template:Chembox image cellTemplate:Chembox image cellTemplate:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox SolubilityInWaterTemplate:Chembox HazardsTemplate:Chembox headerbarTemplate:Chembox Datapage checkTemplate:Yesno
Potassium bis(trimethylsilyl)amide
Template:Longitem Template:Unbulleted list
Abbreviations KHMDS
ChEBI Template:Unbulleted list
ChemSpider Template:Unbulleted list
DrugBank Template:Unbulleted list
EC Number Template:Unbulleted list
KEGG Template:Unbulleted list
Template:Longitem Template:Unbulleted list
RTECS number Template:Unbulleted list
UN number 3263
Script error: No such module "collapsible list".
Script error: No such module "collapsible list".
Template:Longitem Template:Chem/link
Molar mass 199.4831 g mol−1
Appearance White, opaque crystals
Template:Longitem Lithium bis(trimethylsilyl)amide

Sodium bis(trimethylsilyl)amide

Template:Chembox Footer/tracking container onlyScript error: No such module "TemplatePar".Template:Short description

Potassium bis(trimethylsilyl)amide (commonly abbreviated as KHMDS, Potassium(K) HexaMethylDiSilazide) or potassium hexamethyldisilazane[1] is the chemical compound with the formula ((CH3)3Si)2NK. It is a strong, non-nucleophilic base with an approximate pKa of 26 (compare to lithium diisopropylamide, at 36).Script error: No such module "Unsubst".

Structure

The methylsilyl groups give KHMDS good solubility in most organic solvents. Solution structures are either solvated monomers or dimers (or mixtures thereof) with this depending on the coordinating power, concentration, and temperature of the solvent.[2] In general, weakly coordinating solvents such as toluene and N,N-dimethylethylamine give dimers, where as THF and diglyme gave monomers at high dilution.[2] In the solid state, the unsolvated compound is dimeric, with two potassium and two nitrogen atoms forming a square.[3] KHMDS conducts electricity poorly in solution and in the melt, which is attributed to very strong ion pairing.

See also

References

  1. a b Script error: No such module "citation/CS1".
  2. a b Script error: No such module "Citation/CS1".
  3. Script error: No such module "Citation/CS1".