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The reaction of [Re(CO)3(H2O)3]Br or [Re(CO)5Cl] with two peptides, glycylglycine, or glycylalanine were investigated. Each reaction produced a unique, well-defined product. Structural elucidation showed the formation of chiral compounds with the formula [Re(CO)3(Gly-Xxx-O)]2, Xxx = Gly ( 1), Ala ( 2). Each dimer displays C2 symmetry and a nearly rectangular shape. The ligands are bound through the amine and amide carbonyl at a rhenium center and through the pendant carboxylate to the adjacent rhenium center. Both products are fully characterized by X-ray structure elucidation. [ABSTRACT FROM AUTHOR]

Cobalt complexes of N-confused porphyrins and benziphthalocyanine, which both feature organometallic bonds at the macrocycle cores, catalyze the cyclopropanation of styrene with a higher trans-selectivity than the corresponding porphyrin and phthalocyanine complexes. [ABSTRACT FROM AUTHOR]

The new fluorescent chromophore BOPHY can be readily synthesized in two steps from commercially available reagents via the coupling of pyrrole-2-carbox-aldehyde with hydrazine followed by reaction with BF3. The resultant symmetric and dimeric tetracycle is composed of two BF2 units in six-membered chelate rings appended with pyrrole units on the periphery. The quantum yields of fluorescence for the unmodified compound and the tetramethyl variant are near unity, with values of 95 and 92%, respectively, in CH2Cl2. We have probed the electronic structure of this compound via cyclic voltammetry and density functional theory analysis. [ABSTRACT FROM AUTHOR]