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Advances in Organometallic Chemistry | 1979

Homogeneous Catalysis of Hydrosilation by Transition Metals

John Leopold Speier

Publisher Summary This chapter describes numerous ways in which soluble complexes of transition metals act as catalysts for the hydrosilation of organic compounds, especially substituted and unsubstituted unsaturated hydrocarbons. The term “hydrosilation” can be used to describe an addition reaction in which compounds with one or more Si–H bonds add to any reagent. The chapter focuses on the effects of structure on reactivity during hydrosilation in homogeneous solutions of platinum catalysts, and point out similarities and differences that are observed with other catalysts. Commonly, when chloroplatinic acid is the source of the catalyst for hydrosilation and sometimes when salts of other metals are used, no effect is observed for some time after it has been added to a mixture of reagents. Then, rather suddenly a rapid reaction can ensue. This “induction period” can in some cases last for a relatively long time, even for hours. An induction period, followed by a very fast exothermic reaction leads to difficult situations when large amounts of reagents are employed. Homogeneous catalysis with metals other than platinum and hydrosilation of acetylenes is also discussed in this chapter.


Journal of Colloid and Interface Science | 1982

Destruction of microorganisms by contact with solid surfaces

John Leopold Speier; James Richard Malek

Abstract Solids upon which organic or inorganic cations had been chemisorbed killed microorganisms at a rate described by a second order rate expression −dS dt = K [surface area/milliliter][S] in which S = concentration of viable organisms/milliliter in an aqueous medium. Cations that have no antimicrobial activity in solution were capable of forming antimicrobial surfaces.


Journal of Organometallic Chemistry | 1984

Equilibria between MexSiCl4−x, x=3, 2, 1, 0 and alkyl carboxylate esters

Godfrey C. Mbah; John Leopold Speier

Abstract At 150°C equilibria are established between chlorosilanes and alkyl esters according to the equation: Me x SiCl 4- x + RCOOR′ → Me x Si(O 1 2 ) y (OOCR) z-y Cl 4- x-y-z + y RCOCl + z R′Cl When x = 3, y = 0, z = 0.56, when x = 1, y = 0.26, z = 098 When x = 1, y = z = 0.56; when x = 0, y = z = 0.53 Lewis acid salts such as ZnCl 2 or FeCl 3 are effective catalysts for the reactions leading to mixtures of these compounds.


Archive | 1961

Nitrogen-containing cyclic silanes, their preparation and hydrolysis

John Leopold Speier


Archive | 1979

Method of reducing the number of microorganisms in a media and a method of preservation

James Richard Malek; John Leopold Speier


Archive | 1961

Aminated mono-organosilanes and method of dyeing glass therewith

John Leopold Speier


Archive | 1978

Preparation of alkyl polysulfides

John Leopold Speier


Archive | 1993

Process for forming siloxane bonds

Debora Frances Bergstrom; Binh Thanh Nguyen; John Leopold Speier; Ming-Shin Tzuo


Archive | 1975

Method of preparing mercaptans

John Leopold Speier


Archive | 1983

Apparatus for rapidly freezing molten metals and metalloids in particulate form

John Leopold Speier; Donald Taylor Liles

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