Search PubMed⌕ Search

Biomedical subjects

Mark S Mashuta

Publications and source records attributed to Mark S Mashuta.

8 recordsLinked to original sources
PubMed2003

Synthesis and characterization of N2S3X-Fe models of iron-containing nitrile hydratase.

A series of iron complexes based on the pentadentate ligand 4,7-bis(2'-methyl-2'-mercaptopropyl)-1-thia-4,7-diazacyclononane), (bmmp-TASN)(2)(-), have been synthesized and characterized as models of iron-containing nitrile hydratase (NHase). The chloro derivative [(bmmp-TASN)Fe(III)Cl].0.5EtOH (1) contains a labile chloride which facilitates synthesis of related complexes via substitution reactions. Complex 1 is high-spin, g = 4.28. Addition of NEt(4)CN with 1 in CH(2)Cl(2) results in the cyanide ligated complex [(bmmp-TASN)Fe(III)CN] x 0.5EtOH (2), which shows a single intense nu(CN) band at 2083 cm(-)(1) in the IR region. Complex 2 is low-spin, g(1) = 2.31, g(2) = 2.16, and g(3) = 1.96. Under basic conditions complex 1 affords a mu-oxo bridged dimeric Fe(III) complex [(bmmp-TASN)Fe(III)](2)O (3), which shows an intense band at 799 cm(-)(1). Complex 3 was recrystallized from CH(2)Cl(2)/hexane solution in the triclinic space group P1, with a = 10.5486(15) A, b = 13.0612(19) A, c = 8.1852(12) A, alpha = 96.923(2) degrees, beta = 112.729(2) degrees, gamma = 81.048(2) degrees, and Z = 1. Density functional theory (DFT) calculations of the previously communicated iron-nitrosyl complex [(bmmp-TASN)Fe(III)(NO)][BPh(4)] (4) (Inorg. Chem. 2002, 41, 1039-1041) reveal that the HOMO region is dominated by Fe-S bonding. Complexes 1-4 display irreversible or quasi-reversible reductions in the cyclic voltammograms. All of the iron complexes and the zinc derivative, (bmmp-TASN)Zn (5), display an irreversible oxidation. Complex 5 was crystallized in the monoclinic space group P2(1)/n with a = 9.5759(6) A, b = 20.9790(13) A, c = 10.7113(7) A, beta = 91.283(1) degrees, and Z = 4.

Crystallography, X-Ray↗
PubMed2002

Glycyl C(alpha) chemical shielding in tripeptides: measurement by solid-state NMR and correlation with X-ray structure and theory.

We report here (13)C(alpha) chemical shielding parameters for central Gly residues in tripeptides adopting alpha-helix, beta-strand, polyglycine II, and fully extended 2 degrees structures. To assess experimental uncertainties in the shielding parameters and the effects of (14)N-(13)C(alpha) or (15)N-(13)C(alpha) dipolar coupling, stationary and magic angle spinning (MAS) spectra with and without (15)N decoupling were obtained from natural abundance and double-labeled samples containing [2-(13)C, (15)N]Gly. We find that accurate (<1 ppm uncertainty) shielding parameters are measured with good sensitivity and resolution in (15)N decoupled 1D or 2D MAS spectra of double-labeled samples. Compared to variations of isotropic shifts with peptide angles, those of (13)C(alpha) shielding anisotropy and asymmetry are greater. Trends relating shielding parameters to the 2 degrees structure are apparent, and the correlation of the experimental values with unscaled ab initio shielding calculations has an rms error of 3 ppm. Using the experimental data and the ab initio shielding values, the empirical trends relating the 2 degrees structure to shielding are extended to the larger range of torsion angles found in proteins.

Carbon Isotopes↗
PubMed2002

Tris[(1-methylimidazol-2-yl)methyl]amine-boric acid (1/1).

Cocrystallization of a polyimidazole compound with boric acid results in the formation of the title compound, C(15)H(21)N(7).B(OH)(3), which has an extensive hydrogen-bonding network. The O...N(im) separations (im is imidazole) range from 2.6991 (15) to 2.7914 (14) A, with O-H...N angles ranging from 170.6 (18) to 175 (2) degrees. In addition, symmetry-related boric acid molecules form intermolecular hydrogen bonds, with an O...O distance of 2.7582 (14) A, and symmetry-related imidazole groups form pi-pi stacks, with a centroid-to-centroid separation of 3.533 A.

Journal Article↗
PubMed2002

Dichloromethane alkylates a trithiolato-ruthenium complex to yield a methylene-bridged thioether core. Synthesis and structural comparison to the thiolato-ruthenium precursor.

The previously reported triphosphino/trithiolato-ruthenium anion, [tris-(2-diphenylphosphinothia-phenolato)ruthenium(II)](-), [Ru(DPPBT)(3)](-), has been isolated as the PPN salt (PPN = bis(triphenylphosphoranylidene) ammonium), 1, from chlorobenzene/ether as light-orange crystalline plates, and the X-ray crystal structure has been determined. In dichloromethane, the cis positioned thiolates are alkylated by solvent yielding the methylene-bridged triphosphino/dithioether/thiolato complex [(bis-(2-diphenylphosphinothiaphenolato)methane)(2-diphenyl-phosphinothiaphenolato)ruthenium(II)]chloride, [Ru((DPPBT)(2)CH(2))(DPPBT)]Cl (2). Dichloromethane solutions of 1 layered with hexanes yield 2 as orange cubes. The ruthenium-sulfur bond distances in the alkylated, thioether product are slightly shorter than in the thiolate precursor. Within 2, the iron-thioether bond distances are comparable to the iron-thiolate distances.

Journal Article↗
PubMed2002

cis-Dioxocyclam.

Molecules of 1,4,8,11-tetraazacyclotetradecane-5,7-dione, or cis-dioxocyclam, C(10)H(20)N(4)O(2), lie across mirror planes in space group Cmca; the crystal structure reveals interleaved columns of cis-dioxocyclam molecules along the 2(1) screw axis parallel to the crystallographic b axis. The columns are interconnected in a chain-like arrangement by an amido hydrogen-bonding network (N* * *O = 2.816 A) and an amino hydrogen-bonding network (N* * *N = 3.193 A). The intracolumn spacing is 9.02 A.

Journal Article↗
PubMed2002

First [Fe-NO](6) complex with an N(2)S(3)Fe-NO core as a model of NO-inactivated iron-containing nitrile hydratase. Are thiolates and thioethers equivalent donors in low-spin iron complexes?

The spectroscopic and structural properties of [(bmmp-TASN)FeNO]BPh(4) (1) (bmmp-TASN = 4,7-bis(2'-methyl-2'-mercaptopropyl)-1-thia-4,7-diazacyclononane) have been determined and are compared with the nitric oxide inactivated form of iron-containing nitrile hydratase, NHase(dark). [(bmmp-TASN)FeNO]BPh(4) is prepared from the addition of NO to (bmmp-TASN)FeCl followed by addition of sodium tetraphenylborate. [(bmmp-TASN)FeNO]BPh(4) crystallizes from acetonitrile-methanol solutions upon ether vapor diffusion as dark blue plates in the monoclinic space group P2(1)/c with a = 11.9521(14) A, b = 11.3238(13) A, c = 26.624(3) A, beta = 98.280(2), and Z = 4. The nu(NO) stretching frequency of 1856 cm(-)(1) and the Mössbauer parameters, delta = 0.06 mm/s and DeltaE(q) = 1.75 mm/s, compare favorably with those of NHase(dark). The similarities of the iron-sulfur bond distances to the thiolate, 2.284(2) A and 2.291(2) A, versus thioether, 2.285(2) A, are attributed to the low-spin configuration of the iron. The relationship between this structural observation and the spectroscopic properties of the complex are discussed.

Binding Sites↗