Compounds in which an anionic site
Y−
(originally on carbon, but now including other atoms) is attached directly to a heteroatom
X+ (usually nitrogen, phosphorus or sulfur)
carrying a formal positive charge.
They are thus 1,2-dipolar species of the type
RmX+–Y−Rn.
If X is a saturated atom of an element from the first row of the periodic system,
the ylide is commonly represented by a charge-separated form; if X is a second, third,
etc. row element uncharged canonical forms are available
RmX=YRn. If X is an unsaturated atom, doubly bonded to another first row element Z, the negative
charge on Y may be stabilized by
π-
conjugation,
Z=X+–Y−RnZ−–X+=YRn.
Such ylides belong to the class 1,3
dipolar compounds.
However, 1,3-
dipolar compounds with only sextet-containing canonical forms
(e.g.
vinylcarbenes ) are not ylides. E.g.
Ph3P+–C−H2Ph3P+=CH2
(often called a Wittig
reagent),
(CH3)3N+–C−H2,
RC≡N+N−–R,
(CH3)2S=CHPh(CH3)2S+–C−HPh.
Note that ylide is a complete word, not to be confused with the suffix -ylide, used
for some radical anions. Subclasses of ylides: Ylides
RmX+–C−R2
having the negative charge on carbon are classified by citing the name of the element
X before the word ylide.
E.g.
nitrogen ylide,
phosphorus ylide,
oxygen ylide,
sulfur ylide.
A further specification may be achieved by citing the class name of
RmX
before the word ylide.
Thus nitrogen ylides include
amine ylides,
R3N+–C−R2,
azomethine ylidesR2C=N+R–C−R2,
nitrile ylides,
RC≡N+–C−R2.
Some authors, who wish to express the positive charge on X, prefer e.g.
ammonium ylides over
amine ylides; such usage varies
according to the heteroatom X and to national custom.
The ylides
RmX+–Y−RmX=Y
(
Y
=
O,
S,
Se,
Te,
NR)
are usually named by citing the name of
RmX
followed by
the
additive nomenclature term for
Y
(oxide, sulfide, selenide, telluride, imide, respectively). E.g.
amine imides; use of the less systematic synonyms
amine imines and aminimines is discouraged. Some classes of ylides are known by trivial names
e.g.
nitrones,
Wittig reagents (synonymous with
phosphonium ylides).
Source:
PAC, 1995, 67, 1307
(Glossary of class names of organic compounds and reactivity intermediates based on
structure (IUPAC Recommendations 1995))
on page 1375
PAC, 1994, 66, 1077
(Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994))
on page 1176