A synthetic route to borylene-bridged poly(ferrocenylene)s.
Institut für Anorganische Chemie, Johann Wolfgang Goethe-Universität Frankfurt, Germany.Angewandte Chemie International Edition (Impact Factor: 11.34). 02/2006; 45(6):920-5. DOI: 10.1002/anie.200503515
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ABSTRACT: Cyclic voltammetry experiments at minielectrodes exhibit less ohmic error for lower polarity solvents when the supporting electrolyte anion is [B(C(6)F(5))(4)](-) rather than one of the smaller traditional anions such as [BF(4)](-), [PF(6)](-), or [ClO(4)](-). Conductance measurements have been performed for [NBu(4)][B(C(6)F(5))(4)] in tetrahydrofuran, dichloromethane, benzotrifluoride, and acetonitrile and compared with results for [NBu(4)](+) salts of several traditional anions in the same solvents. In solvents with dielectric constants of 10 or less, ion association constants, K(A), are as much as 2 orders of magnitude lower with [B(C(6)F(5))(4)](-), TFAB, as the electrolyte anion and the degree of this lowering is related to the acceptor property of the solvent. Analyses carried out on the basis of a Fuoss model attribute this fact to differences in concentrations of contact ion pairs rather than of solvent-separated ion pairs. The greater dissociation of the TFAB ion is attributed to its highly delocalized charge.Analytical Chemistry 12/2004; 76(21):6395-401. · 5.70 Impact Factor
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