Nickel superoxide dismutase (NiSOD) is a metalloenzyme that converts O2*- into H2O2 and O2 by cycling between Ni(II) and Ni(III) oxidation states. Reduced NiSOD contains Ni(II) in a square-planar N2S2 coordination environment formed by two cysteinate S atoms, an amide N, and an amine N to Ni(II). [Me4N](Ni(II)(BEAAM)) represents the first NiN2S2 complex containing Ni in a mixed amine/amide environment. [Me4](Ni(II)(BEAAM)) contains Ni-S bonds at 2.177(2) and 2.137(2) A and Ni-N bonds at 1.989(7) and 1.858(6) A, which compare well with the metalloenzyme. Orange solutions of [Me(4)N](Ni(II)(BEAAM)) in MeCN are diamagnetic and stable toward O2 for weeks. A quasireversible Ni(II/III) redox couple is observed for [Ni(II)(BEAAM)](NMe4) at 0.12(1) V vs Ag/AgCl. These data suggest that NiSOD utilizes the mixed amine/amide ligands to modulate the Ni(II/III) redox couple to best match the O2*- reduction/oxidation couples while maintaining O2 stability.

Metacognition has been shown to lead to deeper, more durable, and more transferable learning (Bransford, Brown, & Cocking, 2000). This article describes a case study in which metacognition was introduced to undergraduate science (chemistry) classrooms. Students came to understand the difference between superficial memorization and real learning through specific classroom interventions, which were also designed to help students develop metacognitive learning strategies. The aim of the study was to instruct educators how to incorporate metacognition in college science classrooms, and the improved cognitive and affective learning of students indicated its significance. On the basis of students' reflections, we assert that implementation of these strategies will contribute to increased learning not just in chemistry but also across other courses and curricula.

Reaction of the new cyanoscorpionate ligand, hydrotris(4-cyano-3-phenyl)pyrazolylborate (Tp(Ph),(4CN)) with Co(II), Mn(II), and Fe(II) unexpectedly results in the isolation only of crystals containing sandwich complexes in which the ligands have been isomerized to produce the heterocyanoscorpionate hydrobis(4-cyano-3-phenylpyrazolyl)(4-cyano-5-phenylpyrazolyl)borate (Tp(Ph),(4CN*)). The three complexes have been characterized crystallographically and are isostructural, with each ligand acting in a tridentate manner toward the metal. The isomerization of the ligand appears to be more facile than that of the analogous non-cyano ligand, Tp(Ph), with which crystals of the unisomerized sandwich compound have been isolated for Mn(II) and Fe(II).

A new cyanoscorpionate ligand, hydrotris(3- t-butyl-4-cyanopyrazolyl)borate (Tp ( t-Bu,4CN )) is reported. Both Tp ( t-Bu,4CN ) and hydrotris(4-cyano-3-phenylpyrazolyl)borate (Tp (Ph,4CN)) form one-dimensional coordination polymers with Cu(I). The polymeric chains align to form channels which, in the case of Tp ( t-Bu,4CN ), can encapsulate solvent molecules, as evidenced by the characterization of one such polymer with encapsulated acetonitrile molecules.