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Air, sensitivity

Xote 3. Cunulenic ethers are extremely air-sensitive. All operations during the... [Pg.130]

Note 1. Cumulenes are extremely air-sensitive all operations during the work-up must be carried out under nitrogen. [Pg.141]

AH of the [Fe(CN)3] salts maybe considered salts of ferrocyanic acid or tetrahydrogen hexakiscyanoferrate [1712647-5], H4[Fe(CN)3], a strongly acidic, air-sensitive compound. It is soluble in water and alcohol but is insoluble in ether. It can be prepared by precipitation of an etherate by adding ether to a solution of [Fe(CN)3] that was acidified with concentrated sulfuric acid. Removal of the ether of solvation affords a white powder which is stable when dry but slowly turns blue in moist air because of Pmssian Blue formation. [Pg.435]

Iron(II) ediylenediaminetetraacetic acid [15651 -72-6] Fe(EDTA) or A/,Ar-l,2-ethaiiediylbis[A[-(carboxymethyl)glyciQato]ferrate(2—), is a colorless, air-sensitive anion. It is a good reducing agent, having E° = —0.1171, and has been used as a probe of outer sphere electron-transfer mechanisms. It can be prepared by addition of an equivalent amount of the disodium salt, Na2H2EDTA, to a solution of iron(II) in hydrochloric acid. Diammonium [56174-59-5] and disodium [14729-89-6] salts of Fe(EDTA) 2— are known. [Pg.439]

The reaction of a mixture of 1,5,9-cyclododecatriene (CDT), nickel acetylacetonate [3264-82-2], and diethylethoxyalurninum in ether gives red, air-sensitive, needle crystals of (CDT)Ni [12126-69-1] (66). Crystallographic studies indicate that the nickel atom is located in the center of the 12-membered ring of (CDT)Ni (104). The latter reacts readily with 1,5-cyclooctadiene (COD) to yield bis(COD) nickel [1295-35-8] which has yellow crystals and is fairly air stable, mp 142°C (dec) (20). Bis(COD)nickel also can be prepared by the reaction of 1,5-COD, triethylaluminum, and nickel acetylacetonate. [Pg.12]

Plutonium solutions that have a low activity (<3.7 x 10 Bq (1 mCi) or 10 mg of Pu) and that do not produce aerosols can be handled safely by a trained radiochemist in a laboratory fume hood with face velocity 125—150 linear feet per minute (38—45 m/min). Larger amounts of solutions, solutions that may produce aerosols, and plutonium compounds that are not air-sensitive are handled in glove boxes that ate maintained at a slight negative pressure, ca 0.1 kPa (0.001 atm, more precisely measured as 1.0—1.2 cm (0.35—0.50 in.) differential pressure on a water column) with respect to the surrounding laboratory pressure (176,179—181). This air is exhausted through high efficiency particulate (HEPA) filters. [Pg.204]

This air-sensitive complex is epr-active, having a (id- ground-state configuration as opposed to a ground-state (87). [Pg.42]

CyclooctatetraenylCompounds. Sandwich-type complexes of cyclooctatetraene (COT), CgH g, are well known. The chemistry of thorium—COT complexes is similar to that of its Cp analogues in steric number and electronic configurations. Thorocene [12702-09-9], COT2Th, (16), the simplest of the COT derivatives, has been prepared by the interaction of ThCl [10026-08-1] and two equivalents of K CgHg. Thorocene derivatives with alkyl-, sdyl-, and aryl-substituted COT ligands have also been described. These compounds are thermally stable, air-sensitive, and appear to have substantial ionic character. [Pg.42]

C3H3)2TiCH2CH=CH2 [12110-59-7] Ti(III) Cpj allyl purple-blue monomeric extremely air-sensitive... [Pg.153]

CsH5)3Ti [39333-58-9] Ti(III) Cp3 green sublimes at 125 extremely air-sensitive gives (C3H3)2Ti(CO)2 with CO under... [Pg.153]

CsH5)2Ti(CO)3 [12129-51-0] carbonyl dark reddish-brown dec ca 90 extremely air-sensitive... [Pg.157]

Owing to the light and air sensitivity of the carotenoids and retinoids, sample handling is a critical issue. It is recommended to conduct extraction of these materials with peroxide-free solvents, to store biological samples at —70° C under argon and in the dark, to perform the analysis under yellow light, and to use reference compounds of high purity (57). [Pg.102]

The first definitive studies of boron hydrides were carried out by Alfred Stock in Germany starting about 1912 (1). Through extensive and now classic synthetic studies, the field of boron hydride chemistry was founded with the isolation of a series of highly reactive, air-sensitive, and volatile compounds of general composition and This accomplishment required the development of basic vacuum line techniques for the... [Pg.227]

The volatile, air-sensitive Hquid species (CH3)2AlB3Hg and (CH3)2GaB3Hg are prepared by the direct reaction of the corresponding main group metal hahde and salts of the [B3Hg] ion, in the absence of solvent (178). The reaction of (CH3)2AlB3Hg and A1(BH 3 results in the species (BH 2AlB3Hg. These small metallaboranes are fluxional in solution and have limited thermal stability at room temperature. [Pg.244]

Iron carbide (3 1), Fe C mol wt 179.56 carbon 6.69 wt % density 7.64 g/cm mp 1650°C is obtained from high carbon iron melts as a dark gray air-sensitive powder by anodic isolation with hydrochloric acid. In the microstmcture of steels, cementite appears in the form of etch-resistant grain borders, needles, or lamellae. Fe C powder cannot be sintered with binder metals to produce cemented carbides because Fe C reacts with the binder phase. The hard components in alloy steels, such as chromium steels, are double carbides of the formulas (Cr,Fe)23Cg, (Fe,Cr)2C3, or (Fe,Cr)3C2, that derive from the binary chromium carbides, and can also contain tungsten or molybdenum. These double carbides are related to Tj-carbides, ternary compounds of the general formula M M C where M = iron metal M = refractory transition metal. [Pg.453]

The copper complex 1s available from Strem Chemicals, Inc., under the name cuprous triflate (benzene complex). The checkers recommend handling the material In a dry box because of Its high moisture and air sensitivity. [Pg.130]

Cupric trifluoromethylsulfonate (copper II triflate) [34946-82-2] M 361.7, pK <-3.0 (for triflic acid). Dissolve in MeCN, add dry Et20 until cloudy and cool at -20° in a freezer. The light blue ppte is collected and dried in a vacuum oven at 130°/20mm for 8h. It has Xmax 737nm (e 22.4M cm ) in AcOH. [J Am Chem Soc 95 330 1973], It has also been dried in a vessel at O.lTorr by heating with a Fischer burner [J Org Chem 43 3422 1978], It has been dried at 110-120°/5mm for Ih before use and forms a benzene complex which should be handled in a dry box because it is air sensitive [Chem Pharm Bull Jpn 28 262 I980-, J Am Chem Soc 95 330 1973]. [Pg.415]

Hexametbylpbosphorous triamide (HMPT) [1608-26-0] M 163.2, m 7.2°, b 49-51°/12mm, 162-164°/12mm, d 0.989, n 1.466. It may contain more than 1% of phosphoric triamide. The yellow oil is first distd at atm press then under reduced press and stored under N2. It is air sensitive, TOXIC, should not be inhaled and is absorbed through the skin. [Mark Org Synth Coll Vol V 602 1973.]... [Pg.428]

Crystalline substance is not rapidly attacked by oxygen, although solutions are air-sensitive the compound is stable to high temperature in the absence of oxygen. [Pg.666]

Although the synthetic approaches taken by these two groups appear more or less straightforward, there are two difficulties associated with the synthesis of these phosphorus maeroeyeles which make these preparations all the more substantial. The first of these problems is the air sensitivity of phosphines, especially primary and secondary... [Pg.274]

Lithium imides (imidolithiums) are air-sensitive compounds of general formula... [Pg.99]

Reduction of fullerenes to fullerides — Reversible electrochemical reduction of Ceo in anhydrous dimethylformamide/toluene mixtures at low temperatures leads to the air-sensitive coloured anions Qo" , ( = 1-6). The successive mid-point reduction potentials, 1/2, at -60°C are -0.82, -1.26, -1.82, -2.33, —2.89 and —3.34 V, respectively. Liquid NH3 solutions can also be used. " Ceo is thus a very strong oxidizing agent, its first reduction potential being at least 1 V more positive than those of polycyclic aromatic hydrocarbons. C70 can also be reversibly reduced and various ions up to... [Pg.285]

CfjCle) is air-sensitive but can readily be proto-nated to give the more stable hexathiol CfifSH). Reduction of CS2 either elcclrochemically or by alkali metals yields which can exist in... [Pg.315]

The product was isolated as white, air-sensitive crystals of the Bp4 and Pp6 salts. [Pg.895]


See other pages where Air, sensitivity is mentioned: [Pg.202]    [Pg.165]    [Pg.224]    [Pg.241]    [Pg.242]    [Pg.438]    [Pg.441]    [Pg.204]    [Pg.153]    [Pg.153]    [Pg.334]    [Pg.37]    [Pg.227]    [Pg.250]    [Pg.411]    [Pg.275]    [Pg.89]    [Pg.263]    [Pg.363]    [Pg.403]    [Pg.461]    [Pg.587]    [Pg.593]    [Pg.593]    [Pg.939]    [Pg.970]    [Pg.971]   
See also in sourсe #XX -- [ Pg.104 ]




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General techniques for handling air-sensitive compounds

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