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ZINC COMPOUND

Zinc usually occurs as the sulfide but significant quantities of the oxide, carbonate, siUcate [14374-77-7] and basic compounds of the latter two are also mined (see ZiNC AND ZINC ALLOYS). [Pg.419]

Zinc forms salts with acids but since it is amphoteric, it also forms zincates, eg, [Zn(OH)2 H20] and Z.n([7) ). The tendency of zinc to form stable hydroxy complexes is also important because some basic zinc salts are only slightly soluble in water. Examples are 3Zn(OH)2 ZnSO [12027-98-4] and 4Zn(OH)2 ZnCl2 [11073-22-6] which may precipitate upon neutralization of acidic solutions of the salts. [Pg.419]

Properties of zinc salts of inorganic and organic salts are Hsted in Table 1 with other commercially important zinc chemicals. In the dithiocarbamates, 2-mercaptobenzothiazole, and formaldehyde sulfoxylate, zinc is covalendy bound to sulfur. In compounds such as the oxide, borate, and sihcate, the covalent bonds with oxygen are very stable. Zinc—carbon bonds occur in diorganozinc compounds, eg, diethjizinc [557-20-0]. Such compounds were much used in organic synthesis prior to the development of the more convenient Grignard route (see Grignard reactions). [Pg.419]

The water solubiUty of zinc compounds varies greatly, as shown in Table 1. Water-soluble compounds not Hsted are zinc formate [557-41-5] chlorate [10361-95-2] fluorosihcate [16871 -71 -9] and thiocyanate [557-42-6]. Also, the water-soluble amino and cyanide complexes have many uses. [Pg.419]

Zinc compounds are generally colorless unless the other component, eg, chromate, is colored. The lack of color of most zinc compounds in visible light is a great advantage in that they do not color paint films, plastics, mbber, cosmetics, etc. However, when excited by various types of radiation and at various temperatures, zinc oxide, sulfide, selenide [1315-09-9], and related compounds exhibit luminescence, ie, they emit colored light (see Luminescent materials). Zinc-based phosphors can be produced in many colors, depending upon the added dopants. They are used in television tubes, luminescent glasses, and various specialty products. [Pg.419]

Zinc forms salts with acids but since it is amphoteric, it also forms zincates, eg, [Zn(OH)2 and [Zn(OH)J . The tendency of zinc to form [Pg.419]

The coupling of aryl- and alkenylzinc reagents with various halides has widespread use in the cross-coupling of aromatic rings [101]. The reactions of zinc derivatives of aromatic and heteroaromatic compounds with aryl and heterocyclic halides have wide synthetic applications [103,104], [Pg.60]

The reaction of aryl and alkenyl halides with the Reformatsky reagent 237 in polar solvents affords a-arylacetates [105], Iodides of heterocyclic compounds such as pyridine, quinoline and pyrimidine react smoothly with Reformatsky reagents. The cross-coupling of 237 with 4-iodo-2,6-dimethyl- and 2-iodo-4,6-dimethylpyrimidine (236) occurs smoothly to form 238. But no reaction of 5-iodo-2,4-dimethylpyrimidine (239) takes place [106], [Pg.60]

Triflates are used in this reaction [107]. 5-Phenyltropone 241 is prepared by the coupling of triflate 240 with PhZnCl [108], Instead of rather expensive triflates, triflate equivalents such as phenyl mesylates [100], fluoroalkanesulfonates [109] and the fluorosulfonate 242 [110] are used for the coupling. [Pg.60]

As another alternative to triflates, aryl nonaflates (ONf) are easily prepared from phenol and commerically available perfluorobutane sulfonyl fluoride 243, and used for Pd-catalysed coupling with halides [111]. Aryl nonaflates are more reactive than aryl triflates. / -Iodophcnyl nonaflate (244) gives 245 by chemoselective reaction of the [Pg.60]

The coupling of alkenyl iodides or bromides with alkylzinc reagents is also catalyzed by Co complexes. Using Co(acac)3 as a catalyst precursor, the coupling product 260 is obtained in THF NMP in good yield at room temperature [114], [Pg.62]

Crystal Structure, Mechanical and Thermal Properties Tables 4.1-132 -4.1-139. [Pg.665]

Zinc selenide ZnSe n F43m fee Zinc blende Fig. 4.1-131 [Pg.665]

Zinc selenide ZnSe 5.266 Shock wave experiment [Pg.665]

Under normal pressure, ZnS sublimes before melting [Pg.666]

At room temperature, ZnS bulk material consists predominantly of the cubic j ase, often with hexagonal inclusions, leading to polytypic material. Epitaxial ZnS has mostly been grown on GaAs and thus has pseudomorphically assumed the cubic structure of the substrate material. In this section, all data refer to the cubic modification unless explicitly stated otha-wise. [Pg.665]


Zn — Zn in acid solution —0-76 volts) Apart from possible Zn and Zn2 in some melts all zinc compounds are in the +2 state, generally in octahedral or tetrahedral co-ordination. Readily forms complexes, particularly with O and N ligands. [Pg.433]

Sulfite concentrations for scavenging oxygen ate typically in the 100— 300 mg/L range. Zinc compounds for sulfide scavenging ate used at concentrations of 1.4—14 kg/m (0.5—5 lb/bbl) synthetic magnetite concentrations range to 140 kg/m (50 lb/bbl) and higher if the need arises. [Pg.184]

Whereas the worldwide production of 2inc oxide [1314-13-2] is estimated to be around 500,000 t aimuaHy, only about 75,000—100,000 t are used for pigmentary appHcations by the paint industry. About 250,000 t are consumed by the mbber industry, and the rest is used in the production of plastics, paper, cosmetics, pharmaceutical products, ceramics, and glass (see Zinc compounds). [Pg.7]

Antimicrobial agents are used where there is a need to inhibit bacterial and fungal growth. The additives can consist of copper, germanium, zinc and zinc compounds, metal oxides or sulfides, metal zeofltes, as well as silver and copper oxide-coated inorganic core particles (154—159) (see Industrial ANTIMICROBIAL AGENTS). [Pg.257]

Folate antagonists (eg, methotrexate and certain antiepileptics) are used ia treatment for various diseases, but their adininistration can lead to a functional folate deficiency. Folate utilization can be impaired by a depletion of ziac (see Zinc compounds). In humans, the intestinal bmsh border folate conjugase is a ziac metaHoenzyme (72). One study iadicates that the substantial consumption of alcohol, when combiaed with an iaadequate iatake of folate and methionine, may iacrease the risk of colon cancer (73). Based on this study, it is recommended to avoid excess alcohol consumption and iacrease folate iatake to lower the risk of colon cancer. [Pg.42]

Table 1. Properties, Prices, and Uses of Zinc Compounds... Table 1. Properties, Prices, and Uses of Zinc Compounds...
Zinc compound Formula, synonym CAS Registry No. Sp gi Mp, °C Water Other Price, /kg (Aug. 1981) Uses... [Pg.419]


See other pages where ZINC COMPOUND is mentioned: [Pg.419]    [Pg.875]    [Pg.312]    [Pg.527]    [Pg.1084]    [Pg.1084]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1085]    [Pg.1086]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1087]    [Pg.1088]    [Pg.1088]    [Pg.1088]    [Pg.1088]    [Pg.184]    [Pg.210]    [Pg.342]    [Pg.302]    [Pg.419]    [Pg.419]    [Pg.419]    [Pg.420]   
See also in sourсe #XX -- [ Pg.40 ]

See also in sourсe #XX -- [ Pg.743 , Pg.758 ]

See also in sourсe #XX -- [ Pg.622 ]




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A-hetero-substituted organic electrophiles zinc compounds

Aldehydes zinc compound

Alkali-Metal-Zinc Compounds

Allylation of carbonyl compounds mediated by zinc

Allylic zinc compounds

Band zinc compounds

Brillouin zinc compounds

Calcium compounds Zinc sulfate

Carbon nucleophiles zinc compounds

Carbonyl compounds reductions, zinc-acetic acid

Complex zinc compounds

Complexes with zinc compounds

Compound zinc blende materials

Compounds of Zinc and Cadmium

Compounds of Zinc, Cadmium and Mercury

Coordination compounds zinc enzymes

Copper, organo- compounds zinc reagents

Crystal zinc compounds

Density zinc compounds

Dicarbonyl compounds Zinc chloride

Dielectric zinc compounds

Effective zinc compounds

Elastic zinc compounds

Electro zinc compounds

Electron ionization zinc compounds

Electronic zinc compounds

Electrophilic allyl derivatives zinc compounds

Electrophilic reactions zinc compounds

Energy zinc compounds

Environmental concerns zinc compounds

Exciton zinc compounds

Flame retardants zinc compounds

Heat zinc compounds

Lattice zinc compounds

Linear zinc compounds

Magnesium-zinc binary compounds

Melting zinc compounds

Metal groups zinc compounds

Niobium zinc compounds

Olefination of Carbonyl Compounds by Zinc and Chromium Reagents

Organometallic compounds of magnesium, zinc, and cadmium

Organometallic compounds of zinc

Organometallic compounds with zinc

Organosilyl Compounds of Zinc, Cadmium and Mercury

Phonon zinc compounds

Reactions with Aryl Zinc Compounds

Reagents zinc compounds

Refractive zinc compounds

Semiconductors zinc compounds

Some Coordination Compounds of Zinc and Silicon

Spin zinc compounds

Substitution reactions asymmetric, with zinc compounds

Substitution reactions with zinc compounds

Tantalum zinc compounds

Thermal zinc compounds

Trichloride zinc compounds

Univalent Compounds of Zinc

Univalent Compounds of Zinc and Cadmium

ZINC compound database

Zinc Compounds Diethylzinc

Zinc Compounds Diphenylzinc

Zinc Compounds Organozinc reagents

Zinc Compounds Reformatsky reagent

Zinc Compounds Simmons-Smith reagent

Zinc Compounds Zirconium chloride

Zinc Compounds chloride

Zinc Compounds couple

Zinc Compounds iodide

Zinc Compounds isopropoxide

Zinc and Cadmium Compounds

Zinc and its compounds

Zinc chloride compound with

Zinc chloride compound with hydrocyanic acid

Zinc complex compounds, anions

Zinc compounds 1,1-dihaloalkenes

Zinc compounds 24-membered ring structures

Zinc compounds 3-iodo-2- propene

Zinc compounds COMPOUND INDEX

Zinc compounds Quinolones

Zinc compounds ZnCl2

Zinc compounds accessibility

Zinc compounds alkenyl-aryl reactions

Zinc compounds alkenylation

Zinc compounds alkylation

Zinc compounds alkylation reactions

Zinc compounds alkynylation

Zinc compounds alkynylation reactions

Zinc compounds arylation

Zinc compounds benzylation reactions

Zinc compounds biaryl synthesis

Zinc compounds carbonylation

Zinc compounds carbonylation/acylation

Zinc compounds chemical behaviors

Zinc compounds coupling reactions

Zinc compounds cyclization

Zinc compounds homocoupling reactions

Zinc compounds industrial uses

Zinc compounds metallated ring systems

Zinc compounds natural products synthesis

Zinc compounds preparation

Zinc compounds propargylic compound reactions

Zinc compounds properties

Zinc compounds reactions

Zinc compounds synthesis

Zinc compounds systems

Zinc compounds thermal properties

Zinc compounds thermodynamic properties

Zinc compounds trifluoromethyl

Zinc compounds trimethylenemethane synthetic equivalent

Zinc coordination compounds

Zinc coordination compounds materials

Zinc cyanide reaction with aromatic compounds

Zinc iodide benzylic compounds

Zinc iodide carbonyl compounds

Zinc, Acetate Compound Powder

Zinc, activated, and the compounds

Zinc, organo- compounds

Zinc, organo- compounds preparation

Zinc, organometallic compounds

Zinc-copper couple benzylic compounds

Zinc-copper couple carbonyl compounds

Zinc-copper couple compounds

Zmc ZINC COMPOUNDS] (Vol

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