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Computational Study of the Substitution Effect on the Mechanism for the Gold(I)‐Catalyzed Ring Expansions of Unactivated Alkynylcyclopropanes
Author(s) -
Kuo TzuNung,
Liao HsinYi
Publication year - 2013
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.201200517
Subject(s) - chemistry , singlet state , cationic polymerization , catalysis , density functional theory , ring (chemistry) , kinetic energy , computational chemistry , polymer chemistry , organic chemistry , excited state , atomic physics , quantum mechanics , physics
The ring expansion reactions of unactivated alkynylcyclopropanes X‐C≡C‐C 3 H 5 → X‐C=C 4 H 5 (X = H, F, Cl, Me, OMe, NMe 2 , CMe 3 ) were examined using the density functional theory calculations. All of the structures were completely optimized at the B3LYP/6‐311++G** level of theory. For clarify the effect of the cationic gold(I), we also added AuPH 3 + as the catalyst into the system and the structures for Au were calculated at the B3LYP/LANL2DZ level of theory. The main finding of this work is that the singlet‐triplet splitting of X‐C≡C‐C 3 H 5 play an important role in determining the kinetic and thermodynamic stability of the unactivated ring expansion reactions. When X‐C≡C‐C 3 H 5 with a smaller singlet‐triplet splitting is utilized, the reaction has a smaller activation energy and a larger exothermicity.