Nitric oxide plays an important role in many biological functions. A metallo derivative in biological systems is a protein-bound dinitrosyl iron complex (DNIC), which results from iron-sulfur cluster degradation in the presence of excess NO. Through model complexes I have examined the fundamental properties of a dithiolato-Fe(NO)2 complex, bismercaptoethandiazacyclooctane iron dinitrosyl or (H+bme-daco)Fe(NO)2 as a biomimic of dicysteinate coordination of [Fe(NO)2]. This complex was prepared and fully characterized in my studies. The DNIC moiety is in its oxidized state, {Fe(NO)2}9. Through reaction studies, monitored by IR spectroscopy (H+N2S2)Fe(NO)2 (N2S2 = bme-dach. Bme-pda) has been shown to transfer NO to FeIII in (TPP)FeCl (TPP = meso-tetraphenylporphyrin) as NO-. The remaining mononitrosyl converts into complex (N2S2)Fe(NO). The (N2S2)Fe(NO) complexes (N2S2 = bme-daco, bme*-daco, bme-dach) were prepared by direct reaction of dimeric [(N2S2)Fe]2 and NO gas. The analogous (N2S2)Co(NO) complex (N2S2 = bme-dach) has also been prepared. The series of square pyramidal (N2S2)M(NO) have been studied by cyclic voltammetry and ν(NO) IR spectroscopy.

Nitric oxide plays an important role in many biological functions. A metallo derivative in biological systems is a protein-bound dinitrosyl iron complex (DNIC), which results from iron-sulfur cluster degradation in the presence of excess NO. Through model complexes I have examined the fundamental properties of a dithiolato-Fe(NO)2 complex, bismercaptoethandiazacyclooctane iron dinitrosyl or (H+bme-daco)Fe(NO)2 as a biomimic of dicysteinate coordination of [Fe(NO)2]. This complex was prepared and fully characterized in my studies. The DNIC moiety is in its oxidized state, {Fe(NO)2}9. Through reaction studies, monitored by IR spectroscopy (H+N2S2)Fe(NO)2 (N2S2 = bme-dach. Bme-pda) has been shown to transfer NO to FeIII in (TPP)FeCl (TPP = meso-tetraphenylporphyrin) as NO-. The remaining mononitrosyl converts into complex (N2S2)Fe(NO). The (N2S2)Fe(NO) complexes (N2S2 = bme-daco, bme*-daco, bme-dach) were prepared by direct reaction of dimeric [(N2S2)Fe]2 and NO gas. The analogous (N2S2)Co(NO) complex (N2S2 = bme-dach) has also been prepared. The series of square pyramidal (N2S2)M(NO) have been studied by cyclic voltammetry and ν(NO) IR spectroscopy.

As inspired by the coordination environment of nickel in NikR and NiSOD, imidazole ligands were incorporated into N2SNiII square planar complexes in order to investigate the electronic and structural features of NiII species containing both imidazole and thiolate ligation. Rare examples of nickel complexes containing such ligand sets in continuous tetradentate (N2N'S) and discontinuous (N2S---N') coordination were synthesized and characterized. A significant finding in these studies is that the plane of the imidazole ligand is oriented perpendicular to the N2SNi plane. Further investigations addressed the orientational preference and stereodynamic nature of flat monodentate ligands (L = imidazoles, pyridine and an N-heterocyclic carbene) bound to planar N2SNi moieties. The solid state molecular structures of planar [N2SNiL]n+ complexes accessed through bridge-splitting reactions of dimeric, thiolate-S bridged [N2SNi]2 complexes, reveal that the plane of the added monodentate ligand orients largely orthogonal to the N2SNiL square plane. Variable temperature 1H NMR characterization of dynamic processes and ground state isomeric ratios of imidazole complexes in their stopped exchange limiting spectra, readily correlate with DFT-guided interpretation of Ni-L rotational activation barriers. Full DFT characterization relates the orientation mainly to steric hindrance derived both from ligand and binding pocket. In the case of the imidazole ligands a minor electronic contribution derives from intramolecular electrostatic interactions (imidazole C-2 C-H[superscript delta]+- - S[superscript delta]- interaction). Our group has firmly established the versatility of the (bme-daco)2-, (bme-dach)2-, and (ema)[left arrow]- ligands to accommodate a number of metals (M = Ni, Zn, Cu, and Fe ), and have demonstrated reactivity of such N2S2M complexes occurs predominately at the S-thiolate sites. As vanadium is of interest for its biological, pharmacological and spectroscopic/analytical probe abilities, vanadyl analogues were explored as mimics of possible chelates formed from Cys-X-Cys binding sites in vivo. The structural and electronic changes from the incorporation of V=O2+ in such dianionic and tetraanionic N2S2 binding pockets is investigated and compared to Ni2+ and Zn2+ in similar N2S2 environments. The nucleophilicity of the S-thiolate in these systems is explored with alkylating agents and W(CO)x. Furthermore, the vanadyl interaction with the CGC peptide, the biological analogue of the tetraanionic N2S2 ligand, was produced and characterized by EPR; its W(CO)x adducts were indentified by ?(CO) infrared spectroscopy.