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71Michael H. Abraham, Javier Gil-Lostes, William E. Acree, Jr, J. Enrique Cometto-Muñiz and William S. Cain.
Solvation parameters for mercury and mercury(ii) compounds: calculation of properties of environmental interest, J. Environ. Monit., 2008, 10, 435. Glen B. Deacon, Peter C. Junk, Graeme J. Moxey, Marites Guino-o and Karin Ruhlandt-Senge.
Metal based synthetic routes to heavy alkaline earth aryloxo complexes involving ligands of moderate steric bulk, Dalton Trans., 2009, 4878. 1.4.15 Organometallic compounds, Nonaqueous Systems and Ternary Aqueous Systems Effect of electron-donor compounds on the reactions of organomercury compounds with polychloromethanes, Bulletin of the Academy of Sciences of the USSR, Division of chemical science Dimerization, Organomercury Compounds in Organic Synthesis Character of reaction of te tranitromethane and halotrinitromethanes with phenylmagnesium chloride, Bulletin of the Academy of Sciences of the USSR, Division of chemical science Structures of Organic Solid Solutions, Mixed Crystals C12H10Hg, Diphenylmercury, Molecules Containing Five or More Carbon Atoms C12H10Hg, NMR Data for Carbon-13 Photochemical formation and reactions of organometallic compounds, Preparative Organic Photochemistry