Interaction between polynuclear aromatic hydrocarbons and sodium ion in poly (oxyethylene)

Shinji Takeoka; Kohji Horiuchi; Eishun Tsuchida

doi:10.1016/0167-2738(92)90050-Y

Interaction between polynuclear aromatic hydrocarbons and sodium ion in poly (oxyethylene)

Shinji Takeoka, Kohji Horiuchi, Eishun Tsuchida

School of Advanced Science and Engineering

Research output: Contribution to journal › Article › peer-review

1 Citation (Scopus)

Abstract

The ion-ion interaction of the ion pairs between radical anions of π-conjugative molecules (polynuclear aromatic hydrocarbons, AR) such as anthracene, phenanthrene or naphthalene, and sodium ion in CH₃(OCH₂CH₂)_xOCH₃ was evaluated from ionic conductivity measurement. The rate of ion-dissociation increased as either the number of (oxyethylene) unit (x) or the electron affinity of AR increased. This indicates that the continuous (oxyethylene) units are more favorable for ion-dissociation and a molecule having higher ability to become a radical anion shows higher rate of dissociation.

Original language	English
Pages (from-to)	175-179
Number of pages	5
Journal	Solid State Ionics
Volume	50
Issue number	1-2
DOIs	https://doi.org/10.1016/0167-2738(92)90050-Y
Publication status	Published - 1992 Jan

ASJC Scopus subject areas

Chemistry(all)
Materials Science(all)
Condensed Matter Physics

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abstract = "The ion-ion interaction of the ion pairs between radical anions of π-conjugative molecules (polynuclear aromatic hydrocarbons, AR) such as anthracene, phenanthrene or naphthalene, and sodium ion in CH3(OCH2CH2)xOCH3 was evaluated from ionic conductivity measurement. The rate of ion-dissociation increased as either the number of (oxyethylene) unit (x) or the electron affinity of AR increased. This indicates that the continuous (oxyethylene) units are more favorable for ion-dissociation and a molecule having higher ability to become a radical anion shows higher rate of dissociation.",

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N2 - The ion-ion interaction of the ion pairs between radical anions of π-conjugative molecules (polynuclear aromatic hydrocarbons, AR) such as anthracene, phenanthrene or naphthalene, and sodium ion in CH3(OCH2CH2)xOCH3 was evaluated from ionic conductivity measurement. The rate of ion-dissociation increased as either the number of (oxyethylene) unit (x) or the electron affinity of AR increased. This indicates that the continuous (oxyethylene) units are more favorable for ion-dissociation and a molecule having higher ability to become a radical anion shows higher rate of dissociation.

AB - The ion-ion interaction of the ion pairs between radical anions of π-conjugative molecules (polynuclear aromatic hydrocarbons, AR) such as anthracene, phenanthrene or naphthalene, and sodium ion in CH3(OCH2CH2)xOCH3 was evaluated from ionic conductivity measurement. The rate of ion-dissociation increased as either the number of (oxyethylene) unit (x) or the electron affinity of AR increased. This indicates that the continuous (oxyethylene) units are more favorable for ion-dissociation and a molecule having higher ability to become a radical anion shows higher rate of dissociation.

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