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Grasselli

D. Lin-Vien, N.B. Colthup, W.G. Fately, J. G. Grasselli, Infrared and Raman Characteristic Frequencies of Organic Molecules, Academic Press, New York, 1991. [Pg.539]

J. G. Grasselli and W. M. Ritchey, CK.CA.tlas of Spectral Data and Physical Constants of Organic Compounds 2nd ed., CRC Press Inc., Boca Raton, Fla., 1975. A. A. Swigar and R. M. Silversteia, Monotepenes, Infrared, Mass, M-NMR, and C-NMR Spectra, and Korats Indices, Aldrich Chemical Co., Inc., Milwaukee, Wis., 1981. [Pg.435]

Proceedings of the ACS Symposium on Structure-Activity Relationships in Heterogeneous Catalysis, Boston, MA, April 22-27,1990 edited by R.K. Grasselli and A.W. Sleight... [Pg.264]

The dimethylformamide is available as technical grade DMF from the Grasselli Chemicals Department of E. I. duPont de Nemours and Company, Wilmington, Delaware. [Pg.76]

Technical grade DMF is available from the Grasselli Chemicals Department of E. I. duPont de Nemours and Company. The 1,4-dichlorobutane was obtained from the Electrochemicals Department, E. I. duPont de Nemours and Company. Technical Baker and Adamson fused chip sodium sulfide assaying 60% sodium sulfide was used. The checkers obtained somewhat lower yields when the appropriate amount of reagent grade Na2S OHjO was employed instead of the technical material. [Pg.90]

G. Fronza, C. Fuganli, P. Grasselli. G. Pcdroc-chi-Fantoni. C. Zirotti, Chem. Lett. 1984, 335. [Pg.259]

R. Bernard . C. Fuganti, P. Grasselli, G. Mari-ltoni. Synthesis 1980. 50. [Pg.679]

C. Fuganti, P. Grasselli in Enzymes in Organic Synthesis R. Porter, S. Clark, Eds.. Ciba Foundation Symposium 111, p 112. Pitman, London 1985. [Pg.679]

Nital. A soln of l-5ml of nitric acid (d 1.42 g/cc) in 100ml of 95% ale, used for etching metals. A nital soln contg about 15% by vol of Grasselli reagent, nitric acid and ethanol, used for etching Bi, decomposed vigorously. Explns were also reported when mtal mixts came in contact with other metals. It is believed that the decompn was caused by the reduction of the nitric acid to oxides, which catalyzed the decompn (Ref 1). [Pg.211]

CA 31,5165 (1937) 4)P.Hayard, Vacuum Stability Tests on Solventless Double Base Powders Containing Various Stabilizers OSRD 5959 (20 Nov 1945), 28 Fig 32 5) J.G. Grasselli ed, Atlas of Spectral Data and Physical Constants for Organic Compounds ,... [Pg.598]

R. DiCosimo, J.D. Burrington, and R.K. Grasselli, Oxidative dehydrodimerization of propylene over a Bi203-La203 oxide ion-conductive catalyst, J. Catal. 102, 234-239 (1986). [Pg.108]

Proceedings of the Third World Congress on Oxidation Catalysis, San Diego, CA, U.S.A., 21-26 September 1997 edited by R.K. Grasselli,S.T.Oyama, A.M. Gaffney and J.E. Lyons Volume 111 Catalyst Deactivation 1997. [Pg.893]


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See also in sourсe #XX -- [ Pg.57 ]

See also in sourсe #XX -- [ Pg.218 , Pg.432 ]

See also in sourсe #XX -- [ Pg.14 , Pg.20 , Pg.33 ]




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