Literature DB >> 12526364

Magnetic interactions in the high-spin iron(III) oxooctaethylchlorinato derivative [Fe(oxoOEC)(Cl)] and its pi-cation radical [Fe(oxoOEC.)(Cl)]SbCl6.

T J Neal1, S J Kang, I Turowska-Tyrk, C E Schulz, W R Scheidt.   

Abstract

The preparation and characterization of the beta-oxochlorin derivative [3,3,7,8,12,13,17,18-octaethyl-(3H)-porphin-2-onato(2-)]iron(III) chloride, [Fe(oxoOEC)(Cl)], and its pi-cation radical derivative [Fe(oxoOEC.)(Cl)]SbCl6 is described. Both compounds have been characterized by single-crystal X-ray structure determinations, IR, UV/vis/near-IR, and Mössbauer spectroscopies, and temperature-dependent magnetic susceptibility measurements. The macrocycles of [Fe(oxoOEC)(Cl)] and [Fe(oxoOEC.)(Cl)]SbCl6 are both saddled, and [Fe(oxoOEC.)(Cl)]-SbCl6 is slightly ruffled as well. [Fe(oxoOEC)(Cl)] shows a laterally shifted dimeric unit in the solid state, with a mean plane separation of 3.39 A and a lateral shift of 7.39 A. Crystal data for [Fe(oxoOEC)(Cl)]: triclinic, space group P1, Z = 2, a = 9.174(2) A, b = 13.522(3) A, c = 14.838(3) A, alpha = 95.79(3) degrees, beta = 101.46(2) degrees, gamma = 104.84(3) degrees. Upon oxidation, the inter-ring geometric parameters increase; the mean plane separation and the lateral shift of the dimeric unit of [Fe(oxoOEC.)(Cl)]SbCl6 are 4.82 and 8.79 A, respectively. Crystal data for [Fe(oxoOEC.)(Cl)]SbCl6: monoclinic, space group Cc, Z = 4, a = 19.8419(13) A, b = 10.027(2) A, c = 22.417(4) A, beta = 96.13(2) degrees. A broad near-IR absorption band appears at 1415 nm for the pi-cation radical, [Fe(oxoOEC.)(Cl)]SbCl6. Zero-field Mössbauer measurements at 4.2 K for both [Fe(oxoOEC)(Cl)] and [Fe(oxoOEC.)(Cl)]SbCl6 confirmed that the oxidation state of the iron atom did not change upon chemical oxidation. Solid-state magnetic susceptibility measurements for [Fe(oxoOEC.)(Cl)]SbCl6 resulted in a large temperature dependence of the magnetic moment that can best be fit with a model that includes a zero-field splitting parameter of D = 6 cm-1, antiferromagnetic intermolecular iron-iron coupling (2JFe-Fe = -0.14 cm-1), antiferromagnetic intramolecular iron-radical coupling (2JFe-r = -76 cm-1), and antiferromagnetic radical-radical coupling (2Jr-r = -13 cm-1).

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Year:  2000        PMID: 12526364     DOI: 10.1021/ic991052w

Source DB:  PubMed          Journal:  Inorg Chem        ISSN: 0020-1669            Impact factor:   5.165


  5 in total

1.  Conformational Distortions of π-Cation Radical (β-Oxoporphyrin)copper(II) Derivatives: [Cu(2,7,12-TrioxoOEHP)][SbCl(6)] and [Cu(2,7-DioxoOEiBC)][SbCl(6)].

Authors:  Ilona Turowska-Tyrk; Seong-Joo Kang; W Robert Scheidt
Journal:  J Porphyr Phthalocyanines       Date:  2011-03-01       Impact factor: 1.811

2.  Metalloporphyrin mixed-valence π-cation radicals: [Fe(oxoOEC(•/2))(Cl)]2SbCl6, structure, magnetic properties, and near-IR spectra.

Authors:  Ming Li; Teresa J Neal; Graeme R A Wyllie; Allen G Oliver; Charles E Schulz; W Robert Scheidt
Journal:  Inorg Chem       Date:  2011-08-02       Impact factor: 5.165

3.  Explorations in metalloporphyrin stereochemistry, physical properties and beyond.

Authors:  W Robert Scheidt
Journal:  J Porphyr Phthalocyanines       Date:  2008       Impact factor: 1.811

4.  Structural and magnetic effects of meso-substitution in alkyl-substituted metalloporphyrinate pi-cation radicals: characterization of [Fe(TalkylP*)(Cl)]SbCl6 (alkyl = ethyl and n-propyl).

Authors:  Ming Li; Teresa J Neal; Graeme R A Wyllie; Charles E Schulz; W Robert Scheidt
Journal:  Inorg Chem       Date:  2010-09-06       Impact factor: 5.165

5.  Oxidation triggers extensive conjugation and unusual stabilization of two di-heme dication diradical intermediates: role of bridging group for electronic communication.

Authors:  Debangsu Sil; Soumyajit Dey; Amit Kumar; Susovan Bhowmik; Sankar Prasad Rath
Journal:  Chem Sci       Date:  2015-10-26       Impact factor: 9.825

  5 in total

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