The direct interaction of the reaction centre (usually, but not
necessarily, an incipient
carbenium centre) with a lone pair of electrons of an atom or
with the electrons of a σ- or π-bond contained within the parent
molecule but not conjugated with the reaction centre. A distinction
is sometimes made between n-, σ- and π-participation. A rate increase
due to neighbouring group participation is known as '
anchimeric
assistance'. '
Synartetic acceleration' is the special case of anchimeric assistance ascribed to participation by electrons
binding a
substituent to a carbon atom in a β-position relative to the
leaving
group attached to the α-carbon atom. According to the underlying
model, these electrons then provide a three-centre bond (or '
bridge')
'
fastening together' (as the word '
synartetic' is intended to
suggest) the α- and β-carbon atoms between which the charge is
divided in the intermediate
bridged ion formed
(and in the
transition state preceding its
formation). The term synartetic acceleration is not widely
used.
Source:
PAC, 1994, 66, 1077
(Glossary of terms used in physical organic chemistry (IUPAC Recommendations 1994))
on page 1145
Cite as:
IUPAC. Compendium of Chemical Terminology, 2nd ed. (the "Gold Book"). Compiled by
A. D. McNaught and A. Wilkinson. Blackwell Scientific Publications, Oxford (1997).
XML on-line corrected version: http://goldbook.iupac.org (2006-) created by M. Nic,
J. Jirat, B. Kosata; updates compiled by A. Jenkins. ISBN 0-9678550-9-8.
https://doi.org/10.1351/goldbook.