Role of singlet and triplet states in aromatic substitution reactions. II. Fluorescence quenching of anisole and p-hydroquinone by acids

1973 ◽  
Vol 77 (11) ◽  
pp. 1345-1347 ◽  
Author(s):  
George F. Vesley ◽  
Barry D. Olafson
2008 ◽  
Vol 07 (04) ◽  
pp. 805-820 ◽  
Author(s):  
XIANGZHU LI ◽  
JOSEF PALDUS

The reduced multireference (RMR) coupled-cluster (CC) method with singles and doubles (RMR CCSD) that employs a modest-size MR CISD wave function as an external source for the most important (primary) triples and quadruples in order to account for the nondynamic correlation effects in the presence of quasidegeneracy, and which is further perturbatively corrected for the remaining (secondary) triples, RMR CCSD(T), is employed to compute the molecular geometry and the energy of the lowest-lying singlet and triplet states, as well as the corresponding singlet–triplet splitting, for all possible isomers of the m, n-pyridyne diradicals. A comparison is made with earlier results that were obtained by other authors, and the role of the multireference effects for both the geometry and the spin multiplicity of the lowest state, as described by the RMR-type methods, is demonstrated on the example of 2,6- and 3,5-pyridynes.


2011 ◽  
Vol 17 (52) ◽  
pp. 14929-14934 ◽  
Author(s):  
Nicolas Chéron ◽  
Laurent El Kaïm ◽  
Laurence Grimaud ◽  
Paul Fleurat-Lessard

1970 ◽  
Vol 11 (19) ◽  
pp. 1657-1660 ◽  
Author(s):  
David I. Schuster ◽  
David H. Sussman

2017 ◽  
Vol 15 (41) ◽  
pp. 8810-8819 ◽  
Author(s):  
Katie J. Emery ◽  
Tell Tuttle ◽  
John A. Murphy

A designed N,N′-dialkyldiketopiperazine (DKP) provides evidence for the role of DKP additives as initiators that act by electron transfer in base-induced homolytic aromatic substitution reactions, involving coupling of haloarenes to arenes.


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