Ab initio computation of electron affinities of substituted benzalacetophenones (chalcones): a new approach to substituent effects in organic electrochemistry
- 1 December 2004
- journal article
- Published by Elsevier in Electrochimica Acta
- Vol. 50 (4) , 1039-1047
- https://doi.org/10.1016/j.electacta.2004.08.003
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Substituent effects on the reduction potentials of benzalacetophenones (chalcones)Electrochimica Acta, 2004
- Binary cooperative complementary nanoscale interfacial materials. Reduction of silver nanoparticles in DMF. Formation of monolayers and stable colloidsPure and Applied Chemistry, 2000
- Nitration of 2,7-Di-tert-butyl-trans-10b,10c-dimethyl-10b,10c-dihydropyrene. Electrochemical inquiry into interaction between substituents in a Hückel 4n+2 systemTetrahedron, 1995
- Density-functional thermochemistry. III. The role of exact exchangeThe Journal of Chemical Physics, 1993
- Development of the Colle-Salvetti correlation-energy formula into a functional of the electron densityPhysical Review B, 1988
- An improved correlation between polarographic reduction potential and huckel lumo energy. Application to non-benzenoid hydrocarbonsTetrahedron, 1986
- The mechanism of electrohydrodimerization of chalcone on mercury from aqueous solutionsJournal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1985
- Mechanism of electrohydrodimerization of chalcone on mercury from aqueous solutions containing strong surfactantsJournal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1984
- Binding energies in atomic negative ionsJournal of Physical and Chemical Reference Data, 1975
- Zur Kenntniss des p‐DimethylamidobenzaldehydesEuropean Journal of Inorganic Chemistry, 1902