TY - JOUR
T1 - Structure and reactivity/selectivity control by oriented-external electric fields
AU - Shaik, Sason
AU - Ramanan, Rajeev
AU - Danovich, David
AU - Mandal, Debasish
N1 - Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2018/7/21
Y1 - 2018/7/21
N2 - This is a tutorial on use of external-electric-fields (EEFs) as effectors of chemical change. The tutorial instructs readers how to conceptualize and design electric-field effects on bonds, structures, and reactions. Most effects can be comprehended as the field-induced stabilization of ionic structures. Thus, orienting the field along the “bond axis” will facilitate bond breaking. Similarly, orienting the field along the “reaction axis”, the direction in which “electron pairs transform” from reactants- to products-like, will catalyse the reaction. Flipping the field's orientation along the reaction-axis will cause inhibition. Orienting the field off-reaction-axis will control stereo-selectivity and remove forbidden-orbital mixing. Two-directional fields may control both reactivity and selectivity. Increasing the field strength for concerted reactions (e.g., Diels-Alder's) will cause mechanistic-switchover to stepwise mechanisms with ionic intermediates. Examples of bond breaking and control of reactivity/selectivity and mechanisms are presented and analysed from the “ionic perspective”. The tutorial projects the unity of EEF effects, “giving insight and numbers”.
AB - This is a tutorial on use of external-electric-fields (EEFs) as effectors of chemical change. The tutorial instructs readers how to conceptualize and design electric-field effects on bonds, structures, and reactions. Most effects can be comprehended as the field-induced stabilization of ionic structures. Thus, orienting the field along the “bond axis” will facilitate bond breaking. Similarly, orienting the field along the “reaction axis”, the direction in which “electron pairs transform” from reactants- to products-like, will catalyse the reaction. Flipping the field's orientation along the reaction-axis will cause inhibition. Orienting the field off-reaction-axis will control stereo-selectivity and remove forbidden-orbital mixing. Two-directional fields may control both reactivity and selectivity. Increasing the field strength for concerted reactions (e.g., Diels-Alder's) will cause mechanistic-switchover to stepwise mechanisms with ionic intermediates. Examples of bond breaking and control of reactivity/selectivity and mechanisms are presented and analysed from the “ionic perspective”. The tutorial projects the unity of EEF effects, “giving insight and numbers”.
UR - http://www.scopus.com/inward/record.url?scp=85050489077&partnerID=8YFLogxK
U2 - 10.1039/c8cs00354h
DO - 10.1039/c8cs00354h
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C2 - 29979456
AN - SCOPUS:85050489077
SN - 0306-0012
VL - 47
SP - 5125
EP - 5145
JO - Chemical Society Reviews
JF - Chemical Society Reviews
IS - 14
ER -