Document Type

Article

Language

eng

Format of Original

3 p.

Publication Date

9-2008

Publisher

American Chemical Society

Source Publication

Inorganic Chemistry

Source ISSN

0020-1669

Original Item ID

doi: 10.1021/ic801093q

Abstract

A new pentadentate ligand, α,α,α′,α′-tetra(pyrazolyl)lutidine, pz4lut, has been prepared by a CoCl2-catalyzed rearrangement reaction between 2,6-pyridinedicarboxaldehyde and dipyrazolylthione. The coordination chemistry with some divalent first-row transition metal (Mn, Fe, Co, Ni, Cu, and Zn) chlorides has been explored. The electronic properties indicate that the new κ5N ligand is a slightly stronger-field donor to Ni2+ and Co2+ than a related pentadentate ligand with five pyridyl donors presumably because of greater interaction between the metal and axial pyridyl.

Comments

Accepted version. Inorganic Chemistry, Vol. 47, No. 17 (September 2008): 7468–7470. DOI. © American Chemical Society Publications. Used with permission.

Brian Bennett was affiliated with Medical College of Wisconsin at the time of publication.

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