scispace - formally typeset
Search or ask a question
Topic

Yukawa–Tsuno equation

About: Yukawa–Tsuno equation is a research topic. Over the lifetime, 153 publications have been published within this topic receiving 12559 citations.


Papers
More filters
Journal ArticleDOI
TL;DR: The Hammett equation has been widely used for the study and interpretation of organic reactions and their mechanisms as mentioned in this paper, and it is astonishing that u constants, obtained simply from the ionization of organic acids in solution, can frequently predict successfully equilibrium and rate constants for a variety of families of reactions in solution.
Abstract: The Hammett equation (and its extended forms) has been one of the most widely used means for the study and interpretation of organic reactions and their mechanisms. Although the Hammett methodology has been criticized by theoreticians because of its empirical foundation, it is astonishing that u constants, obtained simply from the ionization of organic acids in solution, can frequently predict successfully equilibrium and rate constants for a variety of families of reactions in solution. Almost every kind of organic reaction has been treated via the Hammett equation, or its extended form. The literature is so voluminous and extensive that there is no complete review of all that has been accomplished. Hammett's success in treating the electronic effect of substituents on the rates and equilibria of organic reactions1P2 led Taft to apply the same principles to steric and inductive and resonance effects? Then, more recently, octanol/ water partition coefficients (P) have been used for rationalizing the hydrophobic effects of organic compounds interacting with biological systems? The use of log P (for whole molecules) or n (for substituents), when combined with electronic and steric parameters, has opened up whole new regions of biochemical and pharmacological reactions to study by the techniques of physical organic chemistry.sf3 The combination of electronic, steric, hydrophobic, hydrophilic, and hydrogen-bonding7 parameters has been used to derive quantitative structure-activity relationships (QSAR) for a host of interactions of organic compounds with living systems or parts thereof. The binding of organic compounds to proteins,8 their interaction with enzymess and with cellsloJ1 and tiasues,12 their inhibition of organelles,l' and as antimalarial^'^

6,870 citations

Journal ArticleDOI

1,860 citations

Book
26 Oct 1973
TL;DR: The application of the Hammett equation to data other than side chain reactivities of substituted benzenes has been discussed in this paper, where the separation of inductive, resonance and steric effects is discussed.
Abstract: Preface 1. The Hammett sigma rho relationship 2. Elucidation of reaction mechanisms 3. The separation of inductive, resonance and steric effects: application of the Hammett equation to aliphatic systems 4. Application of the Hammett equation to data other than side chain reactivities of substituted benzenes 5. Thermodynamic aspects of the Hammett equation Problem discussion References Index.

326 citations


Network Information
Related Topics (5)
Intramolecular force
41.6K papers, 772.2K citations
79% related
Reaction rate constant
42.9K papers, 1M citations
78% related
Solvation
21.5K papers, 746.5K citations
77% related
Electron transfer
31.2K papers, 981.1K citations
76% related
Aryl
95.6K papers, 1.3M citations
76% related
Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20172
20161
20151
20141
20138
20122