Literature DB >> 19787893

Indices for predicting the quality of leaving groups.

Paul W Ayers1, James S M Anderson, Juan I Rodriguez, Zobia Jawed.   

Abstract

The inherent quality of leaving groups in chemical reactions is related to their ionization potential and electron affinity using a quadratic model for the dependence of the energy on the number of electrons. A good leaving group for nucleophilic substitution/elimination reactions is one where the difference in energy between the system with the "optimum" number of electrons and the anion is small. Similarly, a good leaving group for electrophilic substitution/elimination reactions is one where the difference in energy between the system with the optimum number of electrons and the cation is small. This insight allows us to define indices for the quality of leaving groups in nucleophilic and electrophilic reactivity, which we term the nucleofugality and the electrofugality, respectively. These indices are useful not only for predicting the quality of leaving groups in organic reactions, but also for explaining the stability of carbocations, carbanions, and trends in pKa.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 19787893     DOI: 10.1039/b500996k

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  5 in total

1.  Protophilicity index and protofelicity equalization principle: new measures of Brønsted-Lowry-Lewis acid-base interactions.

Authors:  Francisco Méndez; Julio A Alonso; Arlette Richaud
Journal:  J Mol Model       Date:  2013-07-07       Impact factor: 1.810

2.  Donation and back-donation analyzed through a charge transfer model based on density functional theory.

Authors:  Ulises Orozco-Valencia; José L Gázquez; Alberto Vela
Journal:  J Mol Model       Date:  2017-06-20       Impact factor: 1.810

3.  UV-spectroscopy, electronic structure and ozonolytic reactivity of sesquiterpenes: a theoretical study.

Authors:  Shu-Xian Hu; Jian-Guo Yu; Eddy Yongping Zeng
Journal:  J Mol Model       Date:  2011-07-16       Impact factor: 1.810

4.  A density functional reactivity theory (DFRT) based approach to understand the interaction of cisplatin analogues with protecting agents.

Authors:  Amrit Sarmah; Ram Kinkar Roy
Journal:  J Comput Aided Mol Des       Date:  2014-09-03       Impact factor: 3.686

5.  Molecular Interactions From the Density Functional Theory for Chemical Reactivity: The Interaction Energy Between Two-Reagents.

Authors:  Ramón Alain Miranda-Quintana; Farnaz Heidar-Zadeh; Stijn Fias; Allison E A Chapman; Shubin Liu; Christophe Morell; Tatiana Gómez; Carlos Cárdenas; Paul W Ayers
Journal:  Front Chem       Date:  2022-06-13       Impact factor: 5.545

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.