Accommodation of the irregular coordination geometry of lead(II) by a square planar N2S2 ligand and its preference for zinc(II). Academic Article

abstract

• The N2S2 ligand, bis-mercaptoethanediazacyclooctane, coordinates to Pb(II) largely through sulfur donors, enlisting a second unit to fulfill an irregular, hemispherical N2S3 coordination environment in which a void suggests the location of a stereochemically active lone pair on Pb(II). That the highly exposed lead is vulnerable to metal ion displacement is demonstrated on reaction with zinc which results in a regular square pyramidal coordination about zinc within a [N2S2Zn]2 dimer. Analysis of the two dimeric structures finds different connectivities of the monomeric subunits account for the stability of the zinc structure over that of the lead.

authors

• Darensbourg, Marcetta

published proceedings

• Inorg Chem

author list (cited authors)

• Golden, M. L., Reibenspies, J. H., & Darensbourg, M. Y.

citation count

• 10

complete list of authors

• Golden, Melissa L||Reibenspies, Joseph H||Darensbourg, Marcetta Y

publication date

• September 2004

publisher

• American Chemical Society (ACS)  Publisher

published in

• Inorganic Chemistry  Journal

keywords

• Rare Diseases

PubMed Central ID

• 15360227

Digital Object Identifier (DOI)

• 10.1021/ic049489d

start page

• 5798

end page

• 5800

volume

• 43

issue

• 19

URL

• http%3A%2F%2Fdx.doi.org%2F10.1021%2Fic049489d