1976•Australian Journal of ChemistryRequires access

The electron affinity of tetracyanoethylene and other organic electron acceptors

LE Lyons, L.D. Palmer

Open publisher page 29 citations

Abstract

Information on the molecular structure of tetracyanoethylene and its mononegative ion is used to derive the electron affinity of tetracyanoethylene from the experimentally determined threshold energy for photodetachment of electrons from the negative ions. The resultant electron affinity of 2.3(± 0.3) eV is 0.6(± 0.4) eV less than a value derived by the magnetron surface ionization technique. Relative electron affinities for the strong electron acceptor organic molecules, which are known from charge-transfer spectra, are placed on an absolute scale using the photodetachment result for tetracyanoethylene.

About this research paper

What this paper is about

Information on the molecular structure of tetracyanoethylene and its mononegative ion is used to derive the electron affinity of tetracyanoethylene from the experimentally determined threshold energy for photodetachment of electrons from the negative ions. The resultant electron affinity of 2.3(± 0.3) eV is 0.6(± 0.4) eV less than a value derived by the magnetron surface ionization technique. Relative electron affinities for the strong electron acceptor organic molecules, which are known from charge-transfer spectra, are placed on an absolute scale using the photodetachment result for tetracyanoethylene.

Why it matters

OpenAlex reports 29 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Information on the molecular structure of tetracyanoethylene and its mononegative ion is used to derive the electron affinity of tetracyanoethylene from the experimentally determined threshold energy for photodetachment of electrons from the negative ions. The resultant electron affinity of 2.3(± 0.3) eV is 0.6(± 0.4) eV less than a value derived by the magnetron surface ionization technique. Relative electron affinities for the strong electron acceptor organic molecules, which are known from charge-transfer spectra, are placed on an absolute scale using the photodetachment result for tetracyanoethylene.

Key concepts: Tetracyanoethylene, Electron affinity (data page), Chemistry, Electron acceptor, Electron, Ion, Acceptor, Molecule

Related papers

Back to paper searchBrowse research topicsOriginal source
The electron affinity of tetracyanoethylene and other organic electron acceptors — Research Paper | ScholarLens