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Strong π-Backbonding Enables Record Magnetic Exchange Coupling Through Cyanide.
Valdez-Moreira, Juan A; Thorarinsdottir, Agnes E; DeGayner, Jordan A; Lutz, Sean A; Chen, Chun-Hsing; Losovyj, Yaroslav; Pink, Maren; Harris, T David; Smith, Jeremy M.
Afiliação
  • Valdez-Moreira JA; Department of Chemistry , Indiana University , 800 East Kirkwood Avenue , Bloomington , Indiana 47405 , United States.
  • Thorarinsdottir AE; Department of Chemistry , Northwestern University , Evanston , Illinois 60208 , United States.
  • DeGayner JA; Department of Chemistry , Northwestern University , Evanston , Illinois 60208 , United States.
  • Lutz SA; Department of Chemistry , Indiana University , 800 East Kirkwood Avenue , Bloomington , Indiana 47405 , United States.
  • Chen CH; Department of Chemistry , Indiana University , 800 East Kirkwood Avenue , Bloomington , Indiana 47405 , United States.
  • Losovyj Y; Department of Chemistry , Indiana University , 800 East Kirkwood Avenue , Bloomington , Indiana 47405 , United States.
  • Pink M; Department of Chemistry , Indiana University , 800 East Kirkwood Avenue , Bloomington , Indiana 47405 , United States.
  • Harris TD; Department of Chemistry , Northwestern University , Evanston , Illinois 60208 , United States.
  • Smith JM; Department of Chemistry , Indiana University , 800 East Kirkwood Avenue , Bloomington , Indiana 47405 , United States.
J Am Chem Soc ; 141(43): 17092-17097, 2019 Oct 30.
Article em En | MEDLINE | ID: mdl-31601108
ABSTRACT
The paramagnetic cyano-bridged complex PhB(tBuIm)3Fe-NC-Mo(NtBuAr)3 (Ar = 3,5-Me2C6H3) is readily assembled from a new four-coordinate, high-spin (S = 2) iron(II) monocyanide complex and the three-coordinate molybdenum(III) complex Mo(NtBuAr)3. X-ray diffraction and IR spectroscopy reveal that delocalization of unpaired electron density into the cyanide π* orbitals leads to a reduction of the C-N bond order. Direct current (dc) magnetic susceptibility measurements, supported by electronic structure calculations, demonstrate the presence of strong antiferromagnetic exchange between spin centers, with a coupling constant of J = -122(2) cm-1. To our knowledge, this value represents the strongest magnetic exchange coupling ever to be observed through cyanide. These results demonstrate the ability of low-coordinate metal fragments to engender extremely strong magnetic exchange coupling through cyanide by virtue of significant π-backbonding into the cyanide ligand.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article