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Organic substitutes

Sulfates. Indium metal and its oxides dissolve in warm sulfuric acid to give a solution of the trisulfate [13464-82-9], In2(S0 2- It is a white, crystalline, deUquescent soHd, readily soluble in water that forms double salts with alkaLi sulfates and some organic substituted ammonium bases. Concentration of the acidified trisulfate solution produces indium acid sulfate crystal [57344-73-7], In(HS0 2> other reaction conditions give basic sulfates. [Pg.81]

Hexachlorocyclotriphosphazene (cycHc trimer) is a respiratory irritant. Nausea has also been noted on exposure (10). Intravenous and intraperitoneal toxicity measurements were made on mice. The highest nonlethal dose (LDq) was measured as 20 mg/kg (11). Linear chloropolymer is also beUeved to be toxic (10). Upon organic substitution, the high molecular weight linear polymers have been shown to be inert. Rat implants of eight different polyphosphazene homopolymers indicated low levels of tissue toxicity (12). EZ has been found to be reasonably compatible with blood (13), and has lower hpid absorption than fiuorosihcone. [Pg.526]

Silicones are probably best known for their application as sealants and as release materials for pressure sensitive adhesives [107]. The silicone polymer combines an inorganic backbone made from silicon-oxygen bonds with organic substitution on the silicon atom. This repeating unit, shown below is called a siloxane. [Pg.505]

The cationic agents used for their antimicrobial activity all fall within the group known as the quaternary ammonium compounds which are variously described as QACs, quats or onium ions. These are organically substituted ammonium compounds as shown in... [Pg.224]

Quaternary ammonium salts are organically substituted nitrogen compounds in which the nitrogen atom is pentavalent. Four of the substituents are alkyl, aryl or heterocyclic radicals and the fifth is an anion (a cationic charge). This anion is mostly chloride. Therefore we call them benzalkonium chlorides. [Pg.133]

Wise, S., Sasse, R.A., and Holmes, H.E. (1984) Organic substitutes for charcoal in black powder type pyrotechnic formulations. US Army Technical Report No. ARBRL-TR-02569. [Pg.412]

The equilibrium as well as the kinetics of hydrolysis and condensation of trialkoxysilanes is influenced by the organic substitution. A special case exists for many aminosilanes such as aminopropyltriethoxysilane, where a stable zwitterionic silanolate forms that is stable in solution [17-19]. It has been reported that at concentrations lower than 0.2% the aminosilane exists as a monomeric silanetriol [19]. [Pg.96]

Linear poly(organophosphazenes) are now synthesized by six different methods. These are (a) The ring-opening polymerization of (NPC12)3 mentioned above, followed by macromolecular substitution (b) Ring-opening polymerization of organic substituted phosphazene cyclic trimers, usually followed by macromolecular substitution ... [Pg.70]

The most important class of silicon-containing polymers that have not yet been covered are the polysilazanes, shown in 7.1. These polymers, or precursors to them, are generally prepared by the reaction of organic-substituted chlorosilanes with ammonia or amines as is shown in reaction (l).32... [Pg.273]

Diene-Iron Carbonyl Complexes and Related Species R. Pettit and G. F. Emerson Reactions of Organotin Hydrides with Organic Compounds Henry C. Kuivila Organic Substituted Cyclosilanes... [Pg.379]

Synthetic Application of Element Organic Substituted Phosphorus Ylides... [Pg.25]

The most important results that throw light on the Si-Si bond are summarized in this review. It deals first with the hydrogen and halogen compounds having Si—Si bonds, describes the preparation and properties of organic substituted disilanes and oligosilanes, and discusses the physicochemical properties of the Si—Si bond. [Pg.3]


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See also in sourсe #XX -- [ Pg.412 ]




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A-hetero-substituted organic electrophiles

A-hetero-substituted organic electrophiles mercury compounds

A-hetero-substituted organic electrophiles research background

A-hetero-substituted organic electrophiles tin compounds

A-hetero-substituted organic electrophiles zinc compounds

Acids, organic halogen-atom substituted

Alkyl-, aryl- and silyl-substituted lithium organics

Chloro-substituted aromatic organic

Heteroaryl-substituted lithium organics

Heteroatom-substituted lithium organics

Natural products synthesis 3-hetero-substituted organic electrophiles

Nucleophilic aromatic substitution organic reaction mechanisms

Nucleophilic substitution reactions organic synthesis

Organic Halogen Compounds Substitution and Elimination Reactions

Organic Halogen Substitution and Elimination Reactions

Organic Substituted Cyclosilanes

Organic Substituted Disilanes

Organic chemistry bimolecular substitution

Organic chemistry electrophilic substitution reaction

Organic chemistry nucleophilic substitution reaction

Organic chemistry substituted carbocations

Organic chemistry substitution reaction

Organic chemistry unimolecular substitution

Organic compounds substitution reactions

Organic compounds substitutive-type nomenclature

Organic reaction mechanisms nucleophilic substitution reactions

Organic reaction mechanisms substitution/elimination

Organic reaction mechanisms unimolecular substitution reactions

Organic reaction mechanisms unimolecular/bimolecular substitutions

Organic reactions electrophilic aromatic substitution

Organic substitution

Organic-solvent-substituted single crystals

Photochemical Substitution Reactions in Synthetic Organic Chemistry

Silyl-substituted lithium organics

Study 6.7 Organic synthesis substituted cyclopropanes

Substitution Organic chemistry

Substitution, organic reactions

Takumichi Sugihara 2 Palladium-Catalyzed Cross-Coupling with Other a-Hetero-Substituted Organic Electrophiles

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