Crystal structure and Hirshfeld surface analysis of {2-[bis-(pyridin-2-ylmeth-yl)amino]-ethane-1-thiol-ato}-chlorido-cadmium(II).

The title compound, [Cd(CHNS)Cl] or [CdCl] (), where = 2-[bis-(pyridin-2-ylmeth-yl)amino]-ethane-1-thiol, was prepared and structurally characterized. The Cd complex crystallizes in 2/ with a distorted trigonal-bipyramidal metal coordination geometry. Supra-molecular inter-actions in include parallel offset face-to-face inter-actions between inversion-related pyridyl rings and potential hydrogen bonds with chlorine or sulfur as the acceptor.

Crystal structure and Hirshfeld surface analysis of -tetra-bromido-1κ,3κ-tetra-kis-(μ-2-{[(pyridin-2-yl)meth-yl]amino}-ethane-1-thiol-ato-κ,:)tetra-mercury(II).

The macrometallacyclic title compound, [HgBr(CHNS)] or [((Hg )(HgBr))] () where = 2-{[(pyridin-2-yl)meth-yl]amino}-ethane-1-thiol, was prepared and structurally characterized. The Hg complex crystallizes in the 2/ space group. The centrosymmetric HgS metallacycle is constructed from metal ions with alternating distorted tetra-hedral BrS and distorted seesaw NS primary coordination environments with pendant pyridyl groups.

Homo- and Heteronuclear Group 12 Metallothionein Type B Cluster Analogs: Synthesis, Structure, H NMR and ESI-MS.

Metallothioneins (MTs) are a ubiquitous class of small cysteine-rich metal-binding proteins involved in metal homeostasis and detoxification with highly versatile metal binding properties. Despite the long-standing association of MT with MS and MS metal clusters, synthetic complexes with these core architectures are exceptionally rare. Here, we demonstrate an approach to synthesizing and characterizing aggregates of group 12 metal ions with monocyclic MS cores in acetonitrile solution without the protection of a protein.

Metal Substitution and Solvomorphism in Alkylthiolate-Bridged Zn and HgZn Metal Clusters.

The impact of substituting Hg(II) for Zn(II) in a thiolate-bridged trinuclear cluster with parallels to a metallothionein metal cluster was investigated. A new solvomorph of [Zn(Zn)](ClO) () ( = -(2-pyridylmethyl)--(2-(ethylthiolato)-amine) and five solvomorphs of a new compound [Hg(Zn)](ClO) () were characterized by single-crystal X-ray crystallography. The interplay of hydrogen bonding and aromatic-packing interactions in producing lamellar, 2D lamellar, and columnar arrangements of complex cations in the crystalline state is discussed.

Contrasting coordination behavior of Group 12 perchlorate salts with an acyclic N3O2 donor ligand by X-ray crystallography and (1)H NMR.

An unbranched N3O2 ligand 2,6-bis[((2-pyridinylmethyl)oxy)methyl]pyridine (L1) was used to prepare new mononuclear heteroleptic Group 12 perchlorate complexes characterized by IR, (1)H NMR and X-ray crystallography. Racemic complexes with pentadentate L1 and one to four oxygens from either water or perchlorate bound to a metal ion were structurally characterized. Octahedral [Zn(L1)(OH2)](ClO4)2 (1) and pentagonal bipyramidal [Cd(L1)(OH2)(OClO3)]ClO4 (2) structures were found with lighter congeners.

Structure and isomerization comparison of Zn(II), Cd(II) and Hg(II) perchlorate complexes of 2,6-bis([(2-pyridyl-methyl)amino]methyl)pyridine.

The divalent zinc triad perchlorate coordination chemistry of 2,6-bis([(2-pyridyl-methyl)amino]methyl)pyridine (L) was investigated by X-ray crystallography and solution state (1)H NMR. New complexes [HgL(ClO4)2] (1) and [CdL(ClO4)2] (2) were isolated as bicapped distorted square pyramidal racemates, contrasting with the approximate trigonal bipyramidal structure of [ZnL](ClO4)2 (3). Although rapid inter- and intramolecular exchange is common for simple complexes of zinc triad metal ions, conditions for slow intramolecular isomerization on both the δ and J(HH) time scales were established for 1, 2 and 3.

Carbonate-templated self-assembly of an alkylthiolate-bridged cadmium macrocycle.

In the presence of Cd(ClO4)2 and a base, a new mixed N,S-donor alkylthiolate ligand supported both carbonate formation from atmospheric CO2 and the self-assembly of a novel bicapped puckered (CdS)6 molecular wheel. The remarkable stability of the complex was demonstrated by slow intermolecular ligand exchange on the (2)J(HH) and J((111/113)Cd(1)H) time scales at elevated temperature. Both CO2 and the base were required to convert amorphous "CdLClO4" precipitated in the absence of air to the carbonate complex.

A synthetic model of Hg(II) sequestration.

Tridentate ligand N-(2-pyridylmethyl)-N-(2-(ethylthiolato)amine (L) forms the novel complex [Hg(5)(L)(6)](ClO(4))(4).toluene () with a bicyclo[3.3.

Bis-tridentate Chelates of an Asymmetric Ligand: X-ray Structures and Solution NMR Characterization of Divalent Zinc Triad Metal Ion Complexes of N-(2-pyridylmethyl)-N-(2-(methylthio)ethyl)amine.

Divalent zinc triad metal ion complexes of type M(L)(2)(ClO(4))(2) (L = N-(2-pyridylmethyl)-N-(2-(methylthio)ethyl)amine) with N(4)S(2) metal coordination spheres were isolated and characterized by X-ray crystallography and variable temperature proton NMR. Although bis-tridentate chelates have nine geometric isomers, the crystallographically characterized complexes of all three metal ions had trans facial octahedral coordination geometry with C(i) symmetry. Despite the low coordination number and geometric preferences of d(10) metal ions, which facilitate inter- and intramolecular exchange processes, dilute solutions of these bis-tridentate chelates exhibited slow geometric isomerization.

Methyl gallate.

THE CRYSTAL STRUCTURE OF THE TITLE COMPOUND (SYSTEMATIC NAME: methyl 3,4,5-trihydroxy-benzoate), C(8)H(8)O(5), is composed of essentially planar mol-ecules [maximum departures from the mean carbon and oxygen skeleton plane of 0.0348 (10) Å]. The H atoms of the three hydroxyl groups, which function as hydrogen-bond donors and acceptors simultaneously, are oriented in the same direction around the aromatic ring.

Investigation of group 12 metal complexes with a tridentate SNS ligand by X-ray crystallography and 1H NMR spectroscopy.

Two series of zinc triad complexes containing the ligand 2,6-bis(methylthiomethyl)pyridine (L1) were synthesized and characterized by X-ray crystallography and solution-state 1H NMR spectroscopy. The distorted meridional octahedral M(L1)2(ClO4)2 series includes the first structurally characterized Zn(II) and Cd(II) complexes with N2(SR2)4 coordination spheres. Coordination of HgCl2 and ZnCl2 with 1 equiv of ligand afforded mononuclear, five-coordinate species Hg(L1)Cl2 and Zn(L1)Cl2, respectively, with distorted square-pyramidal and trigonal-bipyramidal geometries.

Solid-state and solution-state coordination chemistry of the zinc triad with the mixed N,S donor ligand bis(2-methylpyridyl) sulfide.

The binding of group 12 metal ions to bis(2-methylpyridyl) sulfide (1) was investigated by X-ray crystallography and NMR. Seven structures of the chloride and perchlorate salts of Hg(II), Cd(II), and Zn(II) with 1 are reported. Hg(1)(2)(ClO(4))(2), Cd(1)(2)(ClO(4))(2), and Zn(1)(2)(ClO(4))(2).

The OxiMax System. Nellcor's new platform for pulse oximetry.

The new OxiMax Pulse Oximetry System includes the Nellcor N-595 Pulse Oximeter and a new line of OxiMax sensor. The main feature of this platform is the digital memory chip inserted within each OxiMax sensor that contains all the calibration and operating characteristics for that individual sensor. It allows an information exchange between the sensor and the monitor improving monitoring performance during difficult acquisition periods.

Sterically demanding multidentate ligand tris[(2-(6-methylpyridyl))methyl]amine slows exchange and enhances solution state ligand proton NMR coupling to (199)Hg(II).

The solution state coordination chemistry of Hg(ClO(4))(2) with tris[(2-(6-methylpyridyl))methyl]amine (TLA) was investigated in acetonitrile-d(3) by proton NMR. Although Hg(II) is a d(10) metal ion commonly associated with notoriously rapid exchange between coordination environments, as many as six ligand environments were observed to be in slow exchange on the chemical shift time scale at select metal-to-ligand ratios. One of these ligand environments was associated with extensive heteronuclear coupling between protons and (199)Hg and was assigned to the complex [Hg(TLA)](2+).

Comparison of Heteronuclear Coupling Constants for Isostructural Nitrogen Coordination Compounds of (111/113)Cd and (199)Hg.

The complexation of Cd(II) by the tripodal ligand tris[(2-pyridyl)methyl]amine and dipodal ligand bis[(2-pyridyl)methyl]amine was investigated by solution-state NMR and X-ray crystallography. Cadmium coordination compounds exhibiting rarely observed solution-state NMR (1)H-(111/113)Cd satellites were characterized. The eight-coordinate complex [Cd(TMPA)(2)](ClO(4))(2).

Correlation of a Solution-State Conformational Change between Mercuric Chloride Complexes of Tris[(2-(6-methylpyridyl))methyl]amine with X-ray Crystallographic Structures.

Solution-state NMR and X-ray crystallography were used to investigate the complexation of HgCl(2) by the potentially tetradentate ligand tris[(6-methyl-2-pyridyl)methyl]amine (TLA) in acetonitrile. A change in the ligand conformation as a function of the metal-to-ligand ratio could be indirectly monitored through large changes in (3)J((1)H(199)Hg) to the methylene protons at -40 degrees C. The solution-state NMR were correlated with two solid-state structures.

Structural basis of muscle O(2) diffusing capacity: evidence from muscle function in situ.

Although evidence for muscle O(2) diffusion limitation of maximal O(2) uptake has been found in the intact organism and isolated muscle, its relationship to diffusion distance has not been examined. Thus we studied six sets of three purpose-bred littermate dogs (aged 10-12 mo), with 1 dog per litter allocated to each of three groups: control (C), exercise trained for 8 wk (T), or left leg immobilized for 3 wk (I). The left gastrocnemius muscle from each animal was surgically isolated, pump-perfused, and electrically stimulated to peak O(2) uptake at three randomly applied levels of arterial oxygenation [normoxia, arterial PO(2) (Pa(O(2))) 77 +/- 2 (SE) Torr; moderate hypoxia, Pa(O(2)): 33 +/- 1 Torr; and severe hypoxia, Pa(O(2)): 22 +/- 1 Torr].

Chronic hypercapnia resets CO2 sensitivity of avian intrapulmonary chemoreceptors.

Avian intrapulmonary chemoreceptors (IPC) are vagal sensory neurons that participate in the control of breathing. IPC action potential frequency is inversely proportional to PCO2, but it is unclear whether low PCO2 or high pH is the immediate stimulus for signal transduction in IPC. To address this question, comparisons were made between single cell neural responses of 34 IPC recorded in 6 anesthetized ducks (Anas platyrhynchos) acclimatized 12 days to 7.

Effect of inspired O2 concentration on leg lactate release during incremental exercise.

The normal rate of blood lactate accumulation during exercise is increased by hypoxia and decreased by hyperoxia. It is not known whether these changes are primarily determined by the lactate release in locomotory muscles or other tissues. Eleven men performed cycle exercise at 20, 35, 50, 92, and 100% of maximal power output while breathing 12, 21, and 100% O2.

Nitric oxide-related inhibition of carotid chemosensory nerve activity in the cat.

The hypothesis that endogenous nitric oxide may play a physiological role in the regulation of carotid chemosensory activity was tested in this study. The nitric oxide synthase (NOS) inhibitors, L-nitro-arginine-methyl ester (L-NAME, 25-200 microM) and NG-monomethyl-L-arginine acetate (L-NMMA, 50 and 100 microM) were used to study its effects on the chemosensory activity of perfused and superfused cat carotid bodies (n = 21) in vitro at 37-37 degrees C. L-NAME elicited slow excitation of the sensory activity as did L-NMMA.

Increased venous PCO2 enhances dynamic responses of avian intrapulmonary chemoreceptors.

We quantified the neural discharge of intrapulmonary chemoreceptors (IPC) innervating the left lungs of anesthetized Pekin ducks. Right and left lungs were separately unidirectionally ventilated. Alternating steps in CO2 concentration (0-6%, 11-s period) were delivered to the left lung under control conditions [mixed venous PCO2, (PVCO2) 43 +/- 4 Torr] and under venous CO2 load conditions (PVCO2 79 +/- 6 Torr).

Calcium deficient diet, acetazolamide and gas exchange characteristics of avian eggshells.

The effects of calcium deficient diet and acetazolamide on the gas exchange characteristics of avian eggshells were independently investigated in two groups of unmated hens (Gallus domesticus). In one group, eggs were collected during both a normal diet (3.00% Ca) and a calcium deficient diet (0.