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Regional atmosphere ethers

Celestial Fire has for its sphere the ethereal region, whence it makes itself felt even to us. The Elementary Fire has for its abode the surface of the earth, and our atmosphere the Central Fire is lodged in the Center of Matter. It is tenacious, viscous, glutinous, and is innate in matter it is digesting, maturing, neither warm, nor burning to the touch it scatters and consumes very little, because its heat is tempered by cold. [Pg.78]

This square planar nickel(ll) complex is stable in air in the solid state, but solutions of the complex react in air to produce oxidation products of unknown composition. For this reason, manipulations of the complex are best performed in an inert atmosphere. The complex is a nonelectrolyte and is soluble in most common organic solvents, including diethyl ether, but not in water. The infrared spectrum of the complex contains an intense broad band in the double-bond region centered at 1610 cm. The electronic spectrum of a solution of the compound in toluene contains several bands 17.9 (e = 107), 23.0 (e 1600), 24.5 (e 4600), 25.9 (e 2700), and 29.4 kK (e 5500). The PMR spectrum of the complex in CDCI3 contains four bands as expected singlet methyl at 5 1.88, methylene at 6 3.13, vinyl doublet at 6 4.51, and a second vinyl doublet at 5 6.63. The vinyl protons of the charged chelate ring are coupled, J = 3 Hz. [Pg.43]

Fig. 10. Loss of ether from the hemietherate of phenylazotribenzoylmethane. (a) Crystal of etherate freshly exposed to the atmosphere and lying on an (010) face, (b) After 6 days at ambient temperature, (c) After 12 days, (d) After 20 days, (e) After 37 days. The crystal was oriented between crossed polaroids so that the unchanged region transmits light. (From Molecular Crystals and Liquid Crystals 11 (1970), in which a color version of this figure appeared as part of Figure 2 facing page 410. Fig. 10. Loss of ether from the hemietherate of phenylazotribenzoylmethane. (a) Crystal of etherate freshly exposed to the atmosphere and lying on an (010) face, (b) After 6 days at ambient temperature, (c) After 12 days, (d) After 20 days, (e) After 37 days. The crystal was oriented between crossed polaroids so that the unchanged region transmits light. (From Molecular Crystals and Liquid Crystals 11 (1970), in which a color version of this figure appeared as part of Figure 2 facing page 410.
Aryl halides tend to be chemically unreactive and include persistent environmental pollutants such as dichloro-diphenyl-trichloroethane (DDT), polychlorinated biphenyls (PCBs), dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and polybrominated diphenyl ethers (PBDEs). Many studies of the photochemistry of halogenated aromatic compounds have been stimulated by environmental concerns, the goal often being to understand whether photolysis is an important sink for these compounds in natural waters - or in the atmosphere.The photochemistry of aryl halides causes problems in this context because many aryl halides have minimal absorption in the region of the tropospheric solar spectrum (>295 nm), and experiments at environmentally irrelevant wavelengths such as 254 nm are... [Pg.750]

The major route for the removal of dimethyl ether from the atmosphere is via its reaction with OH. With an average atmospheric [OH] = 1 x 10 molecule cm , a lifetime of about 4 days is derived. Nighttime removal via reaction with NO3 may also make a minor contribution in polluted urban and rural regions (a lifetime of 17... [Pg.295]


See other pages where Regional atmosphere ethers is mentioned: [Pg.342]    [Pg.894]    [Pg.610]    [Pg.52]    [Pg.321]    [Pg.598]    [Pg.13]    [Pg.14]    [Pg.494]    [Pg.657]    [Pg.96]    [Pg.192]    [Pg.494]    [Pg.44]    [Pg.12]    [Pg.495]    [Pg.479]    [Pg.604]    [Pg.128]    [Pg.177]    [Pg.351]    [Pg.353]    [Pg.640]    [Pg.287]    [Pg.288]    [Pg.276]    [Pg.14]    [Pg.232]    [Pg.322]    [Pg.290]    [Pg.155]    [Pg.635]    [Pg.187]    [Pg.1177]   
See also in sourсe #XX -- [ Pg.358 , Pg.359 ]




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Regional atmosphere

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