Literature DB >> 11457155

Dimeric phenalenyl-based neutral radical molecular conductors.

X Chi1, M E Itkis, K Kirschbaum, A A Pinkerton, R T Oakley, A W Cordes, R C Haddon.   

Abstract

We report the preparation, crystallization, and solid-state characterization of ethyl (3)- and butyl (4)-substituted spiro-biphenalenyl radicals. Both of these compounds are found to be conducting face-to-face pi-dimers in the solid state but with different room-temperature magnetic ground states. At room temperature, 4 exists as a diamagnetic pi-dimer (interplanar separation of approximately 3.1 A), whereas 3 is a paramagnetic pi-dimer (interplanar separation of approximately 3.3 A), and both compounds show phase transitions between the paramagnetic and diamagnetic forms. Electrical resistivity measurements of single crystals of 3 and 4 show that the transition from the high-temperature paramagnetic pi-dimer form to the low-temperature diamagnetic pi-dimer structure is accompanied by an increase in conductivity by about 2 orders of magnitude. This behavior is unprecedented and is very difficult to reconcile with the usual understanding of a Peierls dimerization, which inevitably leads to an insulating ground state. We tentatively assign the enhancement in the conductivity to a decrease in the on-site Coulombic correlation energy (U), as the dimers form a super-molecule with twice the amount of conjugation.

Entities:  

Year:  2001        PMID: 11457155     DOI: 10.1021/ja0039785

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  7 in total

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3.  A 1,3,2-oxazaborolidine dimer derived from (S)-alpha,alpha-diphenylprolinol.

Authors:  Margarita Ortiz-Marciales; Melvin De Jesús; Eduvigis González; Raphael G Raptis; Peter Baran
Journal:  Acta Crystallogr C       Date:  2004-02-10       Impact factor: 1.172

4.  The Design of Radical Stacks: Nitronyl-Nitroxide-Substituted Heteropentacenes.

Authors:  Evgeny Tretyakov; Ashok Keerthi; Martin Baumgarten; Sergey Veber; Matvey Fedin; Dmitry Gorbunov; Inna Shundrina; Nina Gritsan
Journal:  ChemistryOpen       Date:  2017-08-30       Impact factor: 2.911

5.  Tuning the redox non-innocence of a phenalenyl ligand toward efficient nickel-assisted catalytic hydrosilylation.

Authors:  Gonela Vijaykumar; Anand Pariyar; Jasimuddin Ahmed; Bikash Kumar Shaw; Debashis Adhikari; Swadhin K Mandal
Journal:  Chem Sci       Date:  2018-01-31       Impact factor: 9.825

6.  Phenalenyl based neutral radical as a novel electrochromic material modulating visible to short-wave infrared light.

Authors:  Dejan Stekovic; Mikhail E Itkis
Journal:  RSC Adv       Date:  2018-12-18       Impact factor: 3.361

7.  Preservation of the donor-acceptor character of a carbazole-phenalenone dyad upon adsorption on Pt(111).

Authors:  René Ebeling; Narendra P Arasu; Lisa Bensch; Bertram Schulze Lammers; Bernhard Mayer; Thomas J J Müller; Héctor Vázquez; Silvia Karthäuser
Journal:  Nanoscale Adv       Date:  2020-12-08
  7 in total

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