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Aromatic hydrocarbons metal complexes

It is therefore not surprising that the reactivities of arenes and alkanes in electrophilic substitution reactions are very different, with the former being much more active. At the same time, the mechanism of the interaction (oxidative addition) of both saturated and aromatic hydrocarbons with complexes of metals in a low oxidation state is in principle the same. The reactivities of arenes and alkanes in oxidative addition reactions with respect to low-valent metal complexes therefore usually differ insignificantly. Furthermore, a metal complex via the oxidative addition mechanism can easily cleave the C-H bond in olefin or acetylene. [Pg.12]

An appreciation of the extent to which invertebrate species may be exposed to such chemicals comes from considering the effects of complex mixtures. In the North Atlantic ecosystem alone, hundreds of pollutant chemicals have been identified. These include metals, synthetic and chlorinated organics and polycyclic aromatic hydrocarbons. Over 300 aromatic hydrocarbons have been detected in some regions of the Chesapeake Bay, and high concentrations of PCBs have been... [Pg.52]

Azaferrocene reacts with aromatic hydrocarbons in the presence of aluminium chloride, giving rise to the cationic complexes of the type (Ti -arene)(Ti -cyclopenta-dienyl)iron(l+) isolated as BF4 salts [87JOM(333)71]. The complex 28 is obtained by reaction of the sulfane compound [Cp(SMc2)3Fe]BF4 with pentamethyl-pyrrole [88AG(E)579 88AG(E)1468 90ICA(170)155]. The metallic site in this center reveals expressed Lewis acidity (89CB1891). [Pg.123]

Electron transfer reactions involving alkali metals are heterogeneous, and for many purposes it is desirable to deal with a homogeneous electron transfer system. It was noticed by Scott39 that sodium and other alkali metals react rapidly with aromatic hydrocarbons like diphenyl, naphthalene, anthracene, etc., giving intensely colored complexes of a 1 to 1 ratio of sodium to hydro-... [Pg.153]

The palladium(O) complex undergoes first an oxydative addition of the aryl halide. Then a substitution reaction of the halide anion by the amine occurs at the metal. The resulting amino-complex would lose the imine with simultaneous formation of an hydropalladium. A reductive elimination from this 18-electrons complex would give the aromatic hydrocarbon and regenerate at the same time the initial catalyst. [Pg.246]

The solubility of most metals is much higher when they exist as organometallic complexes.4445 Naturally occurring chemicals that can partially complex with metal compounds and increase the solubility of the metal include aliphatic acids, aromatic acids, alcohols, aldehydes, ketones, amines, aromatic hydrocarbons, esters, ethers, and phenols. Several complexation processes, including chelation and hydration, can occur in the deep-well environment. [Pg.799]

Picric acid, in common with several other polynitrophenols, is an explosive material in its own right and is usually stored as a water-wet paste. Several dust explosions of dry material have been reported [1]. It forms salts with many metals, some of which (lead, mercury, copper or zinc) are rather sensitive to heat, friction or impact. The salts with ammonia and amines, and the molecular complexes with aromatic hydrocarbons, etc. are, in general, not so sensitive [2], Contact of picric acid with concrete floors may form the friction-sensitive calcium salt [3], Contact of molten picric acid with metallic zinc or lead forms the metal picrates which can detonate the acid. Picrates of lead, iron, zinc, nickel, copper, etc. should be considered dangerously sensitive. Dry picric acid has little effect on these metals at ambient temperature. Picric acid of sufficient purity is of the same order of stability as TNT, and is not considered unduly hazardous in regard to sensitivity [4], Details of handling and disposal procedures have been collected and summarised [5],... [Pg.687]

Among oxo-metals, osmium tetroxide is a particularly intriguing oxidant since it is known to oxidize various types of alkenes rapidly, but it nonetheless eschews the electron-rich aromatic hydrocarbons like benzene and naphthalene (Criegee et al., 1942 Schroder, 1980). Such selectivities do not obviously derive from differences in the donor properties of the hydrocarbons since the oxidation (ionization) potentials of arenes are actually less than those of alkenes. The similarity in the electronic interactions of arenes and alkenes towards osmium tetroxide relates to the series of electron donor-acceptor (EDA) complexes formed with both types of hydrocarbons (26). Common to both arenes and alkenes is the immediate appearance of similar colours that are diagnostic of charge-transfer absorp-... [Pg.219]

Residual fuel oil is generally more complex than distillate fuels in composition and impurities. Limited data are available, but there are indications that the composition of No. 6 fuel oil includes (volume basis) aromatics (25%), paraffins (15%), naphthenes (45%), and nonhydrocarbon compounds (15%). Polynuclear aromatic hydrocarbons and their alkyl derivatives and metals are important hazardous and persistent components of No. 6 fuel oil. [Pg.74]

Four types of organic amines exist, as shown in Table 4.8 primary amines RNHj, secondary R2NH2, tertiary RsNH, and quaternary R4N (Appendix D). The hydrocarbon chain R is usually of length Cg-Cu, commonly a straight aliphatic chain, but branched chains and aromatic parts also occur. In general the amines extract metal complexes in the order tertiary > secondary > primary. Only long-chain tertiary and—to a smaller extent—quarternary amines are used in industrial extraction, because of their suitable physical properties trioctylam-ine (TOA, 8 carbons per chain) and trilauryl amine (TLA, 12 carbons per chain) are the most frequently used. For simplicity we abbreviate all amines by RN, and their salts by RNH L . [Pg.165]

Wade expanded the 1971 hypothesis to incorporate metal hydrocarbon 7T complexes, electron-rich aromatic ring systems, and aspects of transition metal cluster compounds [a parallel that had previously been noted by Corbett 19) for cationic bismuth clusters]. Rudolph and Pretzer chose to emphasize the redox nature of the closo, nido, and arachno interconversions within a given size framework, and based the attendant opening of the deltahedron after reduction (diagonally downward from left to right in Fig. 1) on first- and second-order Jahn-Teller distortions 115, 123). Rudolph and Pretzer have also successfully utilized the author s approach to predict the most stable configuration of SB9H9 (1-25) 115) and other thiaboranes. [Pg.81]

Crude oil consists mainly of a mixture of paraffinic, naphthenic, and aromatic hydrocarbons with small amounts of metals-containing heterocyclic compounds. The most abundant metals found in oils are those contained in porphyrin or porphyrin-like complexes (nickel, copper, iron, and vanadium). These... [Pg.11]

Argenlalion chromalography, 261 Aromatic acids in human urine, 285 Aromatic hydrocarbons, 69 Arylhydroxylamines, 298 Ascorbic acid, 296 Aspirin, 282 Asymmetric diens, 290 Asymmetrical peaks, 58, 82, 160 AIT, stability constants of metal complexes. 278 Atrazine, 292 Atropine, 297 Axial diffusion mobile phase. 8 stationary phase, 8,9 Aza-arenes, 293 Azoxybenzenes, 298... [Pg.164]

Shul pin and coworkers have demonstrated, in several papers, that other peroxo vanadium complexes closely related to 36, containing in the coordination sphere amino acids, nitrogen-containing bases or weak carboxylic acids, are effective oxidants of satnrated and aromatic hydrocarbons. An accnrate account containing this work, together with results related to the use of other transition metals, has appeared and aU the relevant literature can be found there. [Pg.1116]

The complex FeCo2(CO)9(PC6H5) is black in the crystalline state and purple in solution. It is moderately air sensitive. It has a low solubility in aliphatic hydrocarbons and a moderately good solubility in aromatic hydrocarbons. In cyclohexane solution it shows Vco bands at 2101 (vs), 2059 (vs), 2048 (vs), 2039(vs), 1981 (w), 1969(w)cm 1. It has been used for various types of basic metal cluster reactions.16... [Pg.354]


See other pages where Aromatic hydrocarbons metal complexes is mentioned: [Pg.105]    [Pg.162]    [Pg.214]    [Pg.388]    [Pg.19]    [Pg.313]    [Pg.389]    [Pg.360]    [Pg.367]    [Pg.270]    [Pg.267]    [Pg.201]    [Pg.91]    [Pg.205]    [Pg.142]    [Pg.530]    [Pg.78]    [Pg.16]    [Pg.586]    [Pg.242]    [Pg.261]    [Pg.378]    [Pg.277]    [Pg.229]    [Pg.20]    [Pg.187]    [Pg.167]    [Pg.88]    [Pg.122]    [Pg.267]    [Pg.193]    [Pg.14]    [Pg.167]    [Pg.396]    [Pg.178]   
See also in sourсe #XX -- [ Pg.396 , Pg.398 ]

See also in sourсe #XX -- [ Pg.396 , Pg.398 ]




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Aromatic complexes

Aromatic hydrocarbons, metalations

Aromatics complex

Aromatics complexation

Complexation aromatic hydrocarbons

Hydrocarbons complexes

Metal complexes with aromatic hydrocarbons

Metal-hydrocarbon complexes

Metals hydrocarbons

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