Victor Grignard discovered his famous reaction, the synthesis of organ
omagnesium halides or Grignard reagents from organic halides and magne
sium, in 1900. Up to now, this reaction has proved tremendously useful
in organic and organometallic synthesis, and many of the secrets of i
ts formation, structure, and reactivity have been unravelled. Neverthe
less, organomagnesium chemistry is still vital and full of surprises.
This will be illustrated with a selection of recent developments, admi
ttedly with a strong bias for results from the author's laboratory. Th
e topics presented concern the intermediacy of carbanions during the c
onversion of organic halides to Grignard reagents, the induction of hi
gh coordination numbers of magnesium by (intramolecular) coordination
of crown and polyethers which leads to special structures such as orga
nometallic rotaxanes and catenanes as well as to increased reactivity,
and finally small alpha,omega-di-Grignard reagents with one, two or t
hree carbon atoms between the two magnesiums, which are of interest bo
th for their unique structures and for their application in the synthe
sis of metallacycles and metal-carbene complexes.