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Query: KEGG:D01170 (ZnO)
 13,684 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The dermal irritancy of six zinc compounds was examined in three animal models. In open patch tests involving five daily applications, zinc chloride (1% aqueous solution) was severely irritant in rabbit, guinea-pig and mouse tests, inducing epidermal hyperplasia and ulceration; aqueous zinc acetate (20%) was slightly less irritant. Zinc oxide (20% suspension dilute Tween 80), zinc sulphate (1% aqueous solution) and zinc pyrithione (20% suspension) were not overtly irritant, but induced a marginal epidermal hyperplasia and increased hair growth. Zinc undecylenate (20% suspension) was not irritant. Epidermal irritancy in these studies is related to the interaction of zinc ion with epidermal keratin. The compounds studied were not consistently bacteriostatic in the three species tested.
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PMID:Interspecies variations in response to topical application of selected zinc compounds. 199 6

Exposure to zinc fume may cause metal fume fever, an acute reaction characterized by an invasion of neutrophils into the airways. This investigation was conducted to examine the possibility that Zn2+ and ZnO might stimulate the formation of oxygen radicals by human neutrophils. Luminol-amplified chemiluminescence (CL) was monitored during 2 h from human neutrophils exposed to Zn2+ or ZnO. The response was compared to that of other metal ions and to that of endotoxin and phorbol myristate acetate (PMA). Zn2+ (6-50 microM) gradually caused a 2-6-fold increase of CL that reached an optimum after 70- 80 min. By contrast, Cd2+, Cr2+, Cr3+, Fe2+, Fe3+, Ni2+ or Co2+ in corresponding concentrations did not increase the CL. Similar to Zn2+, endotoxin (40-640 micrograms/ml) caused a 2-5-fold increase of CL with an optimum after 70 min, and endotoxin (40 micrograms/ml) together with Zn2+ (50 microM) synergistically increased the CL. ZnO (12-100 micrograms/ml) also augmented CL, with a 1.5-5-fold increase at 25-100 micrograms/ml ZnO but with a time response similar to that found after PMA stimulation, in which CL peaked after 20-40 min incubation. Both Zn(2+)- and ZnO-induced CL was inhibited by manoalide, a phospholipase A2 inhibitor, with IC50 of 0.25 microM and 0.66 microM respectively. These results indicate that Zn2+ and ZnO both stimulates oxygen radical formation in human neutrophils and that this might contribute to the pathogenesis of zinc fume fever.
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PMID:Novel aspect on metal fume fever: zinc stimulates oxygen radical formation in human neutrophils. 950 61

With the elaboration of high-yielding, high-titer syntheses of 3-dehydroshikimic acid from glucose using recombinant Escherichia coli, oxidation of this hydroaromatic becomes a potential route for synthesis of gallic acid. Conversion of 3-dehydroshikimic acid into gallic acid likely proceeds via initial enolization of an alpha-hydroxycarbonyl and oxidation of the resulting enediol. 3-Dehydroshikimate enolization in water was catalyzed by inorganic phosphate while Zn(2+) was used to catalyze enolization in acetic acid. Enediol oxidation employed Cu(2+) as either the stoichiometric oxidant or as a catalyst in the presence of a cooxidant. Gallic acid was produced in a yield of 36% when 3-dehydroshikimic acid in phosphate-buffered water reacted for 35 h with H2O2 and catalytic amounts of CuSO(4). 3-Dehydroshikimate-containing, phosphate-buffered culture supernatants reacted with stoichiometric amounts of CuCO(3)Cu(OH)(2) and Cu(x)(H(3-x)(PO4)(2) to give gallic acid in yields of 51% in 5 h and 43% in 12 h, respectively. Solutions of 3-dehydroshikimic acid in acetic acid reacted with stoichiometric amounts of Cu(OAc)(2) to afford a 74% yield of gallic acid in 36 h. Acetic acid solutions of 3-dehydroshikimic acid could also be oxidized by air using catalytic quantities of Cu(OAc)(2). ZnO accelerated these oxidations leading to a 67% yield of gallic acid in 4 h when an acetic acid solution of 3-dehydroshikimic acid was reacted with O(2) and a catalytic amount of Cu(OAc)(2).
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PMID:Synthesis of gallic acid: Cu(2+)-mediated oxidation of 3-dehydroshikimic acid. 1103 Oct 8

Perpendicularly orientated ZnO rods have been grown on thin ZnO templates, from aqueous solutions of zinc acetate and hexamethylenetetraamine (HMT); growth along the c-axis of the ZnO crystallites is promoted by the presence of acetate in the bath.
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PMID:Novel low temperature solution deposition of perpendicularly orientated rods of ZnO: substrate effects and evidence of the importance of counter-ions in the control of crystallite growth. 1212 Mar 20

We have synthesized ZnO nanoparticles by precipitation from zinc acetate in a series of n-alkanols from ethanol to 1-hexanol as a function of temperature. In this system, nucleation and growth are relatively fast and, at longer times, the average particle size continues to increase due to diffusion-limited coarsening. During coarsening, the particle volume increases linearly with time, in agreement with the Lifshitz-Slyozov-Wagner (LSW) model. The coarsening rate increases with increasing temperature for all solvents and increases with alkanol chain length. We show that the rate constant for coarsening is determined by the solvent viscosity, surface energy, and the bulk solubility of ZnO in the solvent.
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PMID:Influence of solvent on the growth of ZnO nanoparticles. 1290 35

The solvothermal reaction of zinc(II) acetate with 1,3,5-benzenetricarboxylic acid and 4,4'-bipyridine in 1-butanol and acetic acid solution gives the title complex, [Zn(3)(C(9)H(3)O(6))(2)(C(10)H(8)N(2))(H(2)O)(2)](n). There are two different coordination environments for the Zn atom, namely ZnNO(2)(H(2)O) and ZnO(4); in the latter case, the Zn atom lies on a twofold symmetry axis. Carboxylate-bridged Zn(3)(O(2)C)(6) clusters are connected through 1,3,5-benzenetricarboxylate and 4,4'-bipyridine ligands (which lie about inversion centers), yielding a three-dimensional framework.
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PMID:Polymeric diaquabis[mu4-1,3,5-benzenetricarboxylato(3-)](mu-4,4'-bipyridine)trizinc(II). 1290 61

A reaction of ZnO, HCl, H(3)PO(4), and 2-pyridylpiperazine in THF/H(2)O mixture at 75 degrees C for 72 h produces a new zinc phosphate, [(C(5)NH(5))(C(4)N(2)H(10))][Zn(H(2)PO(4))(2)(HPO(4))], I. Zinc phosphate I consists of single four-ring (S4R) units with terminal phosphoryl groups hanging from the Zn center. On reaction with zinc acetate dihydrate in the presence of water at 100 degrees C, I gave another new zinc phosphate, [(C(5)NH(5))(C(4)N(2)H(10))][Zn(2)(H(2)PO(4))(HPO(4))(PO(4))] x 2H(2)O, II. II has a layer structure with apertures formed by 4- and 8-T atoms (T = Zn, P). An examination of the two structures reveals that I and II are related, II being formed by the direct addition of Zn(2+) ions to I. Room-temperature (31)P MAS NMR studies show the presence of different phosphorus species in both compounds. An in-situ (31)P MAS NMR investigation on the formation of II from I in the presence of Zn(2+) ions and water reveals the transformation to be facile. What is noteworthy in this study is that the structural integrity of the S4Rs has been maintained during the formation of II. Donor-acceptor hydrogen bond interactions and pi-pi interactions involving the pyridyl groups also appear to play subtle roles in both phosphates. This study, the first attempt of its kind, combines the principles of supramolecular organic chemistry with inorganic building units and contributes to our understanding of the formation of framework solids.
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PMID:Synthesis of a single four-ring (S4R) molecular zinc phosphate and its assembly to an extended polymeric structure: a single-crystal and in-situ MAS NMR investigation. 1451 1

We report a method for the preparation of colloidal ZnO-diluted magnetic semiconductor quantum dots (DMS-QDs) by alkaline-activated hydrolysis and condensation of zinc acetate solutions in dimethyl sulfoxide (DMSO). Mechanistic studies reveal that Co(2+) and Ni(2+) dopants inhibit nucleation and growth of ZnO nanocrystals. In particular, dopants are quantitatively excluded from the critical nuclei but are incorporated nearly isotropically during subsequent growth of the nanocrystals. The smaller nanocrystal diameters that result upon doping are explained by the Gibbs-Thompson relationship between lattice strain and crystal solubility. We describe methods for cleaning the nanocrystal surfaces of exposed dopants and for redispersion of the final DMS-QDs. Homogeneous substitutional doping is verified by high-resolution low-temperature electronic absorption and magnetic circular dichroism (MCD) spectroscopies. A "giant Zeeman effect" is observed in the band gap transition of Co(2+):ZnO DMS-QDs. MCD and Zeeman spectroscopies are used to quantify the magnitude of the p-d exchange interaction (N(0)beta) that gives rise to this effect. N(0)beta values of -2.3 +/- 0.3 eV (-18 500 cm(-1)) for Co(2+):ZnO and -4.5 +/- 0.6 eV (-36 300 cm(-1)) for Ni(2+):ZnO have been determined. Ligand-to-metal charge-transfer transitions are observed in the MCD spectra of both Co(2+):ZnO and Ni(2+):ZnO DMS-QDs and are analyzed in the context of an optical electronegativity model. The importance of these charge-transfer states in determining N(0)beta is discussed. Ferromagnetism with T(C) > 350 K is observed in aggregated nanocrystals of Co(2+):ZnO that unambiguously demonstrates the existence of intrinsic high-T(C) ferromagnetism in this class of DMSs.
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PMID:Magnetic quantum dots: synthesis, spectroscopy, and magnetism of Co2+ - and Ni2+-doped ZnO nanocrystals. 1457 Apr 96

Layered basic zinc acetate (LBZA), Zn(5)(OH)(8)(CH(3)COO)(2).2H(2)O, was deposited on glass substrates by a chemical bath deposition (CBD) method using methanolic solutions of zinc acetate dihydrate. The substrates were put into bottles filled with the solutions and sealed up and were kept at 60 degrees C in a drying oven. Immersion time necessary for the deposition of LBZA films was typically more than 28 h. This was a key to inducing heterogeneous nucleation of LBZA through control over a degree of supersaturation in the evolution of a unique, nest-like morphology. Hydration water contained by zinc acetate dihydrate was quantitatively enough to promote hydrolysis of zinc acetate. The LBZA films were transformed into nanocrystalline, porous ZnO films without morphological deformation by heating at 150 degrees C in air. A mechanism of the formation of the nest-like morphology was discussed based on nonaqueous solution reactions, nucleation, and crystal growth during the CBD process.
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PMID:Growth of layered basic zinc acetate in methanolic solutions and its pyrolytic transformation into porous zinc oxide films. 1502 3

Nanoscale zinc oxide (ZnO) rods of diameters close to the Bohr-exciton radius ( approximately 2 nm) can be prepared from a simple acetate precursor, resulting in ligand-capped rods of ZnO, highly dispersible in nonpolar solvents. Zinc oxide, ZnO, is a wide band-gap semiconductor with applications in blue/ultraviolet (UV) optoelectronic devices and piezoelectric devices. We observe self-assembly into uniform stacks of nanorods aligned parallel to each other with respect to the long axis, and photoluminescence measurements provide evidence for one-dimensional quantum confinement.
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PMID:Zinc oxide quantum rods. 1514 98


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