Morine

Gao W, Dickinson L, Grozinger C, Morin F G and Reven L 1996 Self-assembled monolayers of alkylphosphonic acids on metal oxides Langmuir M 6429-35... 

R. W. Ratchffe and G. Alber-Schonberg iu R. B. Morin and M. Gorman, eds.. Chemistry and Biology of fd-Tactam A.ntibiotics, Academic Press, New... 

Morin (hydrate) (2, 3,4, 5,7-pentahydroxyfiavone) [480-16-0] M 302.2, m 289-292", pKj 5.3, pKi 8.74. Stirred at room temperature with ten times its weight of absolute EtOH, then left overnight to settle. Filtered, and evaporated under a heat lamp to one-tenth its volume. An equal volume of water was added, and the ppted morin was filtered off, dissolved in the minimum amount of EtOH and again ppted with an equal volume of water. The ppte was filtered, washed with water and dried at 110° for Ih. (Yield ca 2.5%.) [Perkins and Kalkwarf Anal Ghent 28 1989 1956.] Complexes with W and Zr. 

As shown in Fig. 7.6, the Mossbauer data show a reduction in Morin transition temperature with increasing shock severity. At temperatures below the transition, increasing shock severity causes greater retention of the higher temperature, weak ferromagnetic contribution. The measure of weak ferromagnetic (WF) fraction (the high temperature form) is a sensitive indication of shock modification. 

Eosin Flavonoids Morin Flavonol, fisetin, robinetin Quercetin Rutin condensation products of urea, formaldehyde and methanol [126], pesticide derivatives [127] sweetening agents [128, 129] anion-active and nonionogenic surface-active agents [130] steroids, pesticides [29,132, 133] pesticides [134—137] vanadium in various oxidation states [138] uracil derivatives [139]... 

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