Literature DB >> 12844318

Electronegativities from core-ionization energies: electronegativities of SF5 and CF3.

Jan E True1, T Darrah Thomas, Rolf W Winter, Gary L Gard.   

Abstract

Core-ionization energies have been measured for SF(6) (S 2p), SF(5)SF(5) (S 2p), SF(5)Br (S 2p and Br 3d), and SF(5)CF(3) (S 2p and C 1s). These results, together with others that establish correlations between core-ionization energies and Pauling electronegativities, make it possible to assign group electronegativities to SF(5) and CF(3). This method gives electronegativities for these groups comparable to that of bromine, whereas analysis of the effect of these groups on acidity indicates electronegativities comparable to that of fluorine. Other methods of estimating electronegativity fall between these extremes. These disparities can be understood in part as reflecting the effects of polarizibility of the substituent, which tends to lower both the core-ionization energy and the deprotonation energy, making the electronegativity appear to be less in one case and more in the other. In addition, and possibly more important, the core-ionization energies presented here reflect the effect of the group on an adjacent atom, whereas the acidity reflects the effect on a remote atom. It appears that fluorine has a large effect on an adjacent atom but a relatively small effect on a remote atom. By contrast SF(5) and CF(3) have a relatively small effect on an adjacent atom, but this effect falls off only slowly with distance from the substituent. Thus, the effective electronegativities of CF(3) and SF(5) relative to those of the halogens depend on the site at which the molecule is probed as well as on the process that is under consideration.

Entities:  

Year:  2003        PMID: 12844318     DOI: 10.1021/ic0343298

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  9 in total

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2.  Enhancement on the Surface Hydrophobicity and Oleophobicity of an Organosilicon Film by Conformity Deposition and Surface Fluorination Etching.

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3.  Nematicidal and insecticidal activities of halogenated indoles.

Authors:  Satish Kumar Rajasekharan; Jin-Hyung Lee; Vinothkannan Ravichandran; Jin-Cheol Kim; Jae Gyu Park; Jintae Lee
Journal:  Sci Rep       Date:  2019-02-14       Impact factor: 4.379

4.  Trifluoromethylation of [AuF3 (SIMes)]: Preparation and Characterization of [Au(CF3 )x F3-x (SIMes)] (x=1-3) Complexes.

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5.  Discovery of Novel and Highly Selective Cyclopropane ALK Inhibitors through a Fragment-Assisted, Structure-Based Drug Design.

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Review 7.  (Hetero)aryl-SVI Fluorides: Synthetic Development and Opportunities.

Authors:  Marc Magre; Shengyang Ni; Josep Cornella
Journal:  Angew Chem Int Ed Engl       Date:  2022-04-27       Impact factor: 16.823

8.  Fluorinated derivatives of pyridine-2,4-dicarboxylate are potent inhibitors of human 2-oxoglutarate dependent oxygenases.

Authors:  Lennart Brewitz; Yu Nakashima; Anthony Tumber; Eidarus Salah; Christopher J Schofield
Journal:  J Fluor Chem       Date:  2021-07       Impact factor: 2.050

9.  Diastereoselectivity in the Staudinger reaction of pentafluorosulfanylaldimines and ketimines.

Authors:  Alexander Penger; Cortney N von Hahmann; Alexander S Filatov; John T Welch
Journal:  Beilstein J Org Chem       Date:  2013-11-27       Impact factor: 2.883

  9 in total

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