The charge-transfer constant. A new substituent constant for structure-activity relationships.
Copyright policy )The charge-transfer constant. A new substituent constant for structure-activity relationships.
A new, versatile constant accounting for the pi-complex formation ability of aromatic systems is proposed. The constant is derived from charge-transfer complex data of aromatic species (charge-transfer constant, CT). The applicability of CT in structure-reactivity relations is demonstrated. It is shown that the affinity of various inhibitors (32) and acetylcholinesterase is a function of CT and pi (Hansch hydrophobicity constant).
Chemical Phenomena, Chemistry, Kinetics, Structure-Activity Relationship, Models, Chemical, Benzene Derivatives, Spectrophotometry, Ultraviolet, Carbamates, Cholinesterase Inhibitors, Mathematics
Chemical Phenomena, Chemistry, Kinetics, Structure-Activity Relationship, Models, Chemical, Benzene Derivatives, Spectrophotometry, Ultraviolet, Carbamates, Cholinesterase Inhibitors, Mathematics
selected citations These citations are derived from selected sources.This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).26 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Average influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
Citations provided by BIP!Popularity provided by BIP!