Formation of a one-dimensional stacking structure of π-conjugated nitroxyl radical bearing a 1,2,5-thiadiazole ring and its magnetic property

Masaru Yao, Satoshi Asakura, Masahiro Abe, Hidenari Inoue, Naoki Yoshioka

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

A novel stable organic radical, 7,7-diphenyl-6,7-dihydro[1,2,5] thiadiazolo[3,4-f]quinoline-6-oxyl (1), forms a one-dimensional columnar structure consisting of slipped π-stacks, which is in contrast to dimer formation of the isoelectronic benzologue, 3,3-diphenyl-3,4-dihydrobenzo[f] quinoline-4-oxyl (2). Magnetic susceptibility of 1 obeyed an antiferromagnetic chain model with J = -47 cm-1, while 2 behaved as an isolated doublet spin state even in the dimer.

Original languageEnglish
Pages (from-to)413-417
Number of pages5
JournalCrystal Growth and Design
Volume5
Issue number2
DOIs
Publication statusPublished - 2005 Mar

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Bearings (structural)
Thiadiazoles
quinoline
Dimers
Magnetic properties
dimers
magnetic properties
rings
Magnetic susceptibility
magnetic permeability
nitroxyl
diphenyl

ASJC Scopus subject areas

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

Cite this

Formation of a one-dimensional stacking structure of π-conjugated nitroxyl radical bearing a 1,2,5-thiadiazole ring and its magnetic property. / Yao, Masaru; Asakura, Satoshi; Abe, Masahiro; Inoue, Hidenari; Yoshioka, Naoki.

In: Crystal Growth and Design, Vol. 5, No. 2, 03.2005, p. 413-417.

Research output: Contribution to journalArticle

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