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Enantiomerization of bridged 1,1′-binaphthyls
Ren Yi, Shmaryahu Hoz
Department of Chemistry
Bar-Ilan University
Sichuan University
Research output
:
Contribution to journal
›
Article
›
peer-review
3
Scopus citations
Overview
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Keyphrases
Racemization
100%
1,1′-binaphthyl
100%
Enantiomerization
100%
Transition State
66%
Parent Compounds
66%
Isomerization
66%
Activation Energy
66%
Rod Length
66%
Length Dependence
33%
Twisting Motion
33%
Reaction Rate
33%
Varying Length
33%
Optically Active
33%
Long Distance
33%
C2 Symmetry
33%
Force Constants
33%
Rubber
33%
Microviscosity
33%
Polyphenyls
33%
Glassy State
33%
Binaphthyl
33%
Glassy Polymers
33%
Computational Level
33%
Oligophenyl
33%
Bridged Compounds
33%
Transition State Structure
33%
Rubbery State
33%
Chemistry
Transition State
100%
Reaction Activation Energy
100%
Isomerization
100%
Ground State
50%
Force Constant
50%
Transition State Structure
50%
Microviscosity
50%
Bridged Compound
50%
Earth and Planetary Sciences
Racemization
100%
Activation Energy
66%
Isomerization
66%
Ground State
33%
Polyphenyls
33%
Material Science
Activation Energy
100%
Glassy Polymer
50%