Sep 1, 2007 - Overtone-Induced Photodissociation. Joseph R. Lane. Department of Chemistry, UniVersity of Otago, P.O. Box 56, Dunedin 9054, New Zealand.
from the'colophony of the Pinus Abies tree he gave the name abietic acid. Since the time ... It was found that some of these impurities clung to the acid even when no .... cult to isolate the acid in the pure condition by fractional crystallization.
and rosin esters, the blending of rosin with synthetic resins, the purification of rosin by vacuum distillation, and the production of rosin oil. Since abietic acid is.
Acidity of Aromatic Sulfonic Acids and Their Use as Titrants in Nonaqueous Solvents. D. J. Pietrzyk and Jon. ... Anhydrous Acetic Acid as Nonaqueous Solvent.
fixative properties, which surpass that of the civet and musk, are primarily due to ambreinolide (lo), an odorless component formed by autoxidative degradation ...
Ernest. Wenkert , Adriano. Afonso , J. B-son. Bredenberg , Chikara. Kaneko , Akira. Tahara. Journal of the American Chemical Society 1964 86 (10), 2038-2043.
Note: In lieu of an abstract, this is the article's first page. Click to increase image size Free first page. View: PDF. Citing Articles; Related Content. Citation data is ...
Dec 1, 1997 - The effect of a fluorosulfonic acid (FSO3H) aqueous solution on decomposing the chrysotile asbestos fibers was investigated by using FT-IR, ...
The effect of a fluorosulfonic acid (FSO3H) aqueous solution on decomposing the chrysotile asbestos fibers was investigated by using FT-IR, XRD, and XPS.
Sep 1, 2007 - Fluorosulfonic Acid and Chlorosulfonic Acid: Possible Candidates for OH-Stretching Overtone-Induced Photodissociation. Joseph R. Lane.
Farnum and Mader
214 J . Org. Chem., Vol. 42, No. 2, 1977 reduced under these conditions. The mixture was heated a t 45 "C for 16 h. The remaining Zn-Cu was removed by centrifugation and the supernatant liquid was added to water (100 ml) containing hydrochloric acid (0.5 ml). The water was extracted with pentane (4 X 2 ml), and the pentane was washed with 5% sodium bicarbonate solution and saturated sodium chloride solution. After drying with magnesium sulfate the product (0.285 g, 42%) was isolated by preparative GC (10 f t X 0.25 in. 5%OV-101 a t 45 "C): [ a ] D
