Nature of the inductive effect of azinyl groups
Journal Article
·
· Chem. Heterocycl. Compd. (Engl. Transl.); (United States)
The induction constants of azinyl groups are factored into two components, a sigma-induction (sigma/sub X/) and a field (sigma/sub F/) component. It is shown that the sigma/sub X/ constants of azinyl groups can be thought of as sums of contributions from the phenyl group and the endocyclic nitrogen atoms. A satisfactory correlation is found between the sigma/sub F/ constants and the size and direction of the dipole moment of the heterocyclic substituents in the framework of the Kirkwood-Westheimer equation.
- Research Organization:
- Novosibirsk Institute of Organic Chemistry (USSR)
- OSTI ID:
- 6961729
- Journal Information:
- Chem. Heterocycl. Compd. (Engl. Transl.); (United States), Journal Name: Chem. Heterocycl. Compd. (Engl. Transl.); (United States) Vol. 23:5; ISSN CHCCA
- Country of Publication:
- United States
- Language:
- English
Similar Records
Solvent dielectric attenuation of substituent effects. Dependence on boundary representation in prolate spheroidal cavity models
Influence of the polarization effect on the donor properties of 1-phenylsilatrane
Substituent Dependent Optical Properties of p-phenyl Substituted ethenyl-E-thiophenes
Journal Article
·
Sat Dec 31 23:00:00 EST 1983
· J. Comput. Chem.; (United States)
·
OSTI ID:6013412
Influence of the polarization effect on the donor properties of 1-phenylsilatrane
Journal Article
·
Thu Dec 14 23:00:00 EST 2017
· Russian Chemical Bulletin
·
OSTI ID:22863423
Substituent Dependent Optical Properties of p-phenyl Substituted ethenyl-E-thiophenes
Journal Article
·
Sat Sep 15 00:00:00 EDT 2018
· Journal of Fluorescence (Online)
·
OSTI ID:22795597
Related Subjects
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY
400201* -- Chemical & Physicochemical Properties
640302 -- Atomic
Molecular & Chemical Physics-- Atomic & Molecular Properties & Theory
74 ATOMIC AND MOLECULAR PHYSICS
ACETONE
ANGULAR MOMENTUM
ATOMIC MODELS
AZINES
CARBON 13
CARBON ISOTOPES
CHARGE DISTRIBUTION
CHEMICAL SHIFT
CONFIGURATION INTERACTION
DEUTERIUM COMPOUNDS
DIAMAGNETISM
DIPOLE MOMENTS
DMSO
ELECTRONEGATIVITY
ELECTRONIC STRUCTURE
EVEN-ODD NUCLEI
FLUORINE 19
FLUORINE ISOTOPES
HETEROCYCLIC COMPOUNDS
HYBRIDIZATION
HYDROGEN COMPOUNDS
INDUCTION
ISOTOPES
KETONES
LIGHT NUCLEI
MAGNETISM
MATHEMATICAL MODELS
NMR SPECTRA
NUCLEI
ODD-EVEN NUCLEI
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
ORIENTATION
PARTICLE PROPERTIES
SPECTRA
SPIN
SPIN ORIENTATION
STABLE ISOTOPES
STRUCTURAL CHEMICAL ANALYSIS
SULFOXIDES
400201* -- Chemical & Physicochemical Properties
640302 -- Atomic
Molecular & Chemical Physics-- Atomic & Molecular Properties & Theory
74 ATOMIC AND MOLECULAR PHYSICS
ACETONE
ANGULAR MOMENTUM
ATOMIC MODELS
AZINES
CARBON 13
CARBON ISOTOPES
CHARGE DISTRIBUTION
CHEMICAL SHIFT
CONFIGURATION INTERACTION
DEUTERIUM COMPOUNDS
DIAMAGNETISM
DIPOLE MOMENTS
DMSO
ELECTRONEGATIVITY
ELECTRONIC STRUCTURE
EVEN-ODD NUCLEI
FLUORINE 19
FLUORINE ISOTOPES
HETEROCYCLIC COMPOUNDS
HYBRIDIZATION
HYDROGEN COMPOUNDS
INDUCTION
ISOTOPES
KETONES
LIGHT NUCLEI
MAGNETISM
MATHEMATICAL MODELS
NMR SPECTRA
NUCLEI
ODD-EVEN NUCLEI
ORGANIC COMPOUNDS
ORGANIC NITROGEN COMPOUNDS
ORGANIC SULFUR COMPOUNDS
ORIENTATION
PARTICLE PROPERTIES
SPECTRA
SPIN
SPIN ORIENTATION
STABLE ISOTOPES
STRUCTURAL CHEMICAL ANALYSIS
SULFOXIDES