New Family of Aminophenalenyl-Based Neutral Radical Molecular Conductors: Synthesis, Structure, and Solid State Properties.

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Title: New Family of Aminophenalenyl-Based Neutral Radical Molecular Conductors: Synthesis, Structure, and Solid State Properties.
Authors: Besson, Claire1, Finney, Eric E.1, Finke, Richard G.1 rfinke@lamar.colostate.edu
Source: Journal of the American Chemical Society. 6/8/2005, Vol. 127 Issue 22, p8185-8196. 12p.
Subjects: Free radical reactions, Magnetic susceptibility, Lattice theory, Crystal lattices, Solid state physics, Organometallic compounds
Abstract: We report the preparation, crystallization, and solid-state characterization of the first members of a new family of spiro-bis-(1,9-diamino-substituted-phenalenyl)boron neutral radicals. The crystal structures show that the three radicals are monomeric and without close contacts in the crystal lattice. In all cases magnetic susceptibility measurements confirm the presence of free radicals with one unpaired spin per molecule. Two of the new radical compounds are among the most highly conducting neutral organic solids, with room-temperature conductivities reaching σRT = 4 x 10--² S/cm. The measured conductivities correlate with the closest intermolecular contacts in the solid state and with the calculated band dispersions, even though the bandwidths are much smaller than those found in other organic conductors. [ABSTRACT FROM AUTHOR]
Copyright of Journal of the American Chemical Society is the property of American Chemical Society and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: New Family of Aminophenalenyl-Based Neutral Radical Molecular Conductors: Synthesis, Structure, and Solid State Properties.
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  Data: <searchLink fieldCode="AR" term="%22Besson%2C+Claire%22">Besson, Claire</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Finney%2C+Eric+E%2E%22">Finney, Eric E.</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Finke%2C+Richard+G%2E%22">Finke, Richard G.</searchLink><relatesTo>1</relatesTo><i> rfinke@lamar.colostate.edu</i>
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+the+American+Chemical+Society%22">Journal of the American Chemical Society</searchLink>. 6/8/2005, Vol. 127 Issue 22, p8185-8196. 12p.
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  Data: <searchLink fieldCode="DE" term="%22Free+radical+reactions%22">Free radical reactions</searchLink><br /><searchLink fieldCode="DE" term="%22Magnetic+susceptibility%22">Magnetic susceptibility</searchLink><br /><searchLink fieldCode="DE" term="%22Lattice+theory%22">Lattice theory</searchLink><br /><searchLink fieldCode="DE" term="%22Crystal+lattices%22">Crystal lattices</searchLink><br /><searchLink fieldCode="DE" term="%22Solid+state+physics%22">Solid state physics</searchLink><br /><searchLink fieldCode="DE" term="%22Organometallic+compounds%22">Organometallic compounds</searchLink>
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  Data: We report the preparation, crystallization, and solid-state characterization of the first members of a new family of spiro-bis-(1,9-diamino-substituted-phenalenyl)boron neutral radicals. The crystal structures show that the three radicals are monomeric and without close contacts in the crystal lattice. In all cases magnetic susceptibility measurements confirm the presence of free radicals with one unpaired spin per molecule. Two of the new radical compounds are among the most highly conducting neutral organic solids, with room-temperature conductivities reaching σRT = 4 x 10--² S/cm. The measured conductivities correlate with the closest intermolecular contacts in the solid state and with the calculated band dispersions, even though the bandwidths are much smaller than those found in other organic conductors. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
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  Data: <i>Copyright of Journal of the American Chemical Society is the property of American Chemical Society and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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        Value: 10.1021/Ja0504439
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        Text: English
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      – SubjectFull: Free radical reactions
        Type: general
      – SubjectFull: Magnetic susceptibility
        Type: general
      – SubjectFull: Lattice theory
        Type: general
      – SubjectFull: Crystal lattices
        Type: general
      – SubjectFull: Solid state physics
        Type: general
      – SubjectFull: Organometallic compounds
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      – TitleFull: New Family of Aminophenalenyl-Based Neutral Radical Molecular Conductors: Synthesis, Structure, and Solid State Properties.
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              Text: 6/8/2005
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              Y: 2005
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