Schaffer

Schaffer s acid, CioHg04S. 2-hydroxy-7-naphthalene sulphonic acid. Obtained by sulphonating 2-naphthol with a small amount of sulphuric acid at a higher temperature than is used for the preparation of crocein acid. A valuable dyestuff intermediate. [Pg.353]

Cleveland J P, Schaffer T E and Hansma P K 1995 Probing oscillatory hydration potentials using thermal-mechanical noise in an atomic force microscope Rhys. Rev. B 52 R8692-5... [Pg.1749]

Flauser M J B, Olsen L F, Bronnikova T V and Schaffer W M 1997 J. Phys. Condens. Metter 0 5075 barter R, Olsen L F, Steinmetz C G and Geest T 1993 Chaos in Chemistry and Bioohemistry ed R J Field and L Gydrgyi (Singapore World Scientific) p 175... [Pg.3072]

Altschul S F, T L Madden, A A Schaffer, J Zhang, Z Zhang, W Miller and D J Lipman 1997. Gapped BLAST and PSI-BLAST A New Generation of Protein Database Search Programs. Nucleic Acids Research 25 3389-3402. [Pg.574]

Naphthalenediol. This diol is prepared by the alkah fusion of 2-hydroxynaphthalene-6-sulfonic acid (Schaffer acid) at 290—295°C. Schaffer acid is usually produced by sulfonation of 2-naphthol with the addition of sodium sulfate at 85—105°C. This acid is also used as a coupling component in the production of a2o dyes such as Acid Black 26. 2,6-Naphthalenediol is used as a component in the manufacture of aromatic polyesters which, as is also tme of the corresponding amides, display Hquid crystal characteristics (52). [Pg.500]

E. L. Schaffer, Review of Information Relating to the Charring Rate of Wood, Research Note PPL-0145, U.S. Department of Agriculture, Eorest Service, Eorest Products Laboratory, Madison, Wise., 1966. [Pg.335]

Johnson, L. Schaffer, U. and Schaffer, D. (1994). Oak Ridge National Laboratory The First Fifty Years. Knoxville, TN University of Tennessee Press. [Pg.820]

Two symmetry parameterizations of the angular overlap model of the ligand field. Relation to the crystal field model. C. E. Schaffer, Struct. Bonding (Berlin), 1973,14, 69-110 (33). [Pg.43]

Quantitative comparison of the symmetry components of a ligand field illustrations of the orthonormal operators formalism. M. Brorson, T. Damhus and C. E. Schaffer, Comments Inorg. Chem., 1983,3,1-34 (29). [Pg.47]

Eberson, L., and Schaffer, H. (1971). Organic Electrochemistry , Springer-Verlag Press. [Pg.221]

Raunak KV, Mukherjee S, Poonam PAK, Olsen CE, Schaffer SJC, Sharma SK, Watter-... [Pg.264]

Campbell R, Schaffer CB, TupinJ Catatonia associated with glutethimide withdrawal. J Clin Psychiatry 44 32—33, 1983... [Pg.150]

Harnung SE, Schaffer CE (1972) Phase-fixed 3-G Symbols and Coupling Coefficients for the Point Groups. 12 201-255... [Pg.247]

Schaffer CE (1968) A Perturbation Representation of Weak Covalent Bonding. 5 68-95 Schaffer CE (1973) Two Symmetry Parameterizations of the Angular-Overlap Model of the Ligand-Field. Relation to the Crystal-Field Model. 14 69-110 Scheldt WR, Lee YJ (1987) Recent Advances in the Stereochemistry of Metallotetrapyrroles. 64 1-70... [Pg.254]

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