Argon benzene

The electron temperature (Tg), electron density (ng) and electron energy distribution function for a plasma sustained in an argon/benzene mixture were measured by double and triple plasma-probe methods. Each probe was heated up to 1000 K with a sheathed heater, which was inserted into the probe, in order to prevent... 

Figure 12. Contour map of n, cm- ) for an argon-benzene plasma as a function of total pressure and flow rate of benzene. A flow rate of argon was fixed to 300...

Figure 3 Plot of the stretching force constant vs. origin energy of the <— S monomer transition for the argon - benzene derivative...

Let a be any solute forming a dilute solution in a pure solvent w. We are interested in the change in the solvation Gibbs energy caused by the addition of a small quantity of solute s. We assume here that a has a fixed conformation a can be a simple solute such as argon, benzene, or a single conformer of a large polymer. 

Bromo-3-iodo-l-(4-methylphenylsulfonyl)indole (0.476 g, 1.00 mmol), methyl acrylate (0.108 g, 1.25 mmol), EtjN (0.127 g, 1.25 mmol) and Pd(OAc)2 (11 mg, 0.050 mmol) were mixed in a tube, purged with argon and the tube was sealed and heated to 100°C for 1 h. After cooling, it was opened and mixed with CH2CI2 (50 ml). The solution was washed with water and dried (Na SOJ. The residue was purified by chromatography on silica using 1 3 benzene-hexane for elution. The yield was 0.350 g (81%). 

Nitroso-5//-dibenz[/>,/]azepine (9, R = NO) is relatively stable to photolysis under argon, whereas in benzene solution in the presence of oxygen, irradiation induces an oxidative Fischer -Hepp-type rearrangement to 2-nitro-5//-dibenz[6,/]azepinc (10, R = N02), accompanied by ring contraction to acridine-9-carbaldehyde184 (see also Section 3.2.2.4.). 

A solution of 3.7I g (0.013 mol) of tributyltin hydride in 10 mL benzene is added dropwise to a solution of 3.09 g (0.011 mol) of S-[(S)-4-(benzyloxy)-3-pentenyl] 5-methyl carbonodithioate in 25 mL of degassed, anhyd benzene under an atmosphere of argon, followed by 5 mg of AIBN. The mixture is heated under reflux for 2.5 h and then is concentrated under reduced pressure. Flash chromatography of the residue using ht,0/petroIeum ether 1 50 containing 1 % triethylamine as eluant gives a colorless oil yield 3.87 g (78%) [a] - 26 (e = 1. CHCl3). 

In a 250-ml., three-necked, round-bottomed flask equipped with a mechanical stirrer, a gas inlet, and a stopper are placed 540 mg. (0.00346 mole) of a mixture of cis- and dimethyl sulfoxide (Note 3). While a slight positive pressure of argon is maintained... 

Fig, 37. Far-infrared spectra of chromium, iron, and cobalt atom reactions with benzene, benzene-(f and benzene/benzene-d mixtures in argon matrices at 10-12K 171). 

Argon matrices at 10-12K, unless otherwise noted. The symbols + and - indicate shifts to higher and lower wavenumbers, respectively, Benzene matrix at 77 K. 

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