Triflate
salts are thermally very stable with melting points up to 350 °C for
sodium,
boron and
silver salts especially in water-free form. They can be obtained directly from triflic acid and the metal hydroxide or metal carbonate in water. Alternatively, they can be obtained from reacting metal chlorides with neat triflic acid or
silver triflate, or from reacting
barium triflate with metal sulfates in water: :{{chem2 | MCl_{n} + n HOTf -> M(OTf)_{n} + n HCl }} :{{chem2 | MCl_{n} + n AgOTf -> M(OTf)_{n} + n AgCl↓ }} :{{chem2 | M(SO4) + n Ba(OTf)2 -> M(OTf)_{2n} + BaSO4↓ }} Metal triflates are used as
Lewis acid catalysts in
organic chemistry. Especially useful are the
lanthanide triflates of the type (where Ln is a
lanthanoid). A related popular catalyst
scandium triflate is used in such reactions as
aldol reactions and
Diels–Alder reactions. An example is the
Mukaiyama aldol addition reaction between
benzaldehyde and the
silyl enol ether of
cyclohexanone with an 81%
chemical yield. The corresponding reaction with the
yttrium salt fails: Triflate is a commonly used
weakly coordinating anion. ==See also==