Literature DB >> 11457135

Perchlorophenalenyl radical.

P A Koutentis1, Y Chen, Y Cao, T P Best, M E Itkis, L Beer, R T Oakley, A W Cordes, C P Brock, R C Haddon.   

Abstract

We report the preparation and solid-state characterization of the perchlorophenalenyl radical (1). The radical is initially obtained as a yellow-green solid by reduction of the perchlorophenalenium salt (12(+)). This solid sublimes in a sealed tube to give black shiny hexagonal crystals of the perchlorophenalenyl radical (1). The structure consists of 1-dimensional stacks of the monomeric radical. The peri-chlorine atoms force the phenalenyl system to be strongly nonplanar leading to a large separation between adjacent molecules within the stacks (3.78 A), and the molecules adopt two distinct stacking motifs (quasisuperimposed and rotated by 60 degrees with respect to neighbors). Because of the packing frustration in the lattice and the large intermolecular spacing, the solid shows Curie paramagnetism in the temperature range 100-400 K, before antiferromagnetic coupling sets in at low temperatures. Due to the narrow bandwidth that results from the isolation of the individual molecules, the solid is a Mott-Hubbard insulator, with a room-temperature conductivity of rho(RT) = 10(-10) S/cm.

Entities:  

Year:  2001        PMID: 11457135     DOI: 10.1021/ja0018015

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


  5 in total

1.  Tetra-kis(1,3,4,6,7,9-hexa-aza-1H-phen-alen-6-ium) sodium(I) penta-kis(tetra-fluorido-borate).

Authors:  Yuqin Jiang; Yanhui Hou; Yongsheng Chen
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2008-09-24

2.  A new face of phenalenyl-based radicals in the transition metal-free C-H arylation of heteroarenes at room temperature: trapping the radical initiator via C-C σ-bond formation.

Authors:  Jasimuddin Ahmed; Sreejyothi P; Gonela Vijaykumar; Anex Jose; Manthan Raj; Swadhin K Mandal
Journal:  Chem Sci       Date:  2017-09-12       Impact factor: 9.825

3.  Phenalenyl-fused porphyrins with different ground states.

Authors:  Wangdong Zeng; Sangsu Lee; Minjung Son; Masatoshi Ishida; Ko Furukawa; Pan Hu; Zhe Sun; Dongho Kim; Jishan Wu
Journal:  Chem Sci       Date:  2015-02-04       Impact factor: 9.825

4.  Storing redox equivalent in the phenalenyl backbone towards catalytic multi-electron reduction.

Authors:  Mrinal Bhunia; Sumeet Ranjan Sahoo; Bikash Kumar Shaw; Shefali Vaidya; Anand Pariyar; Gonela Vijaykumar; Debashis Adhikari; Swadhin K Mandal
Journal:  Chem Sci       Date:  2019-06-10       Impact factor: 9.825

5.  Benzo[cd]triangulene: A Spin 1/2 Graphene Fragment.

Authors:  Prince Ravat; Olivier Blacque; Michal Juríček
Journal:  J Org Chem       Date:  2019-10-17       Impact factor: 4.354

  5 in total

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