- secondary phosphine
-
any compound of general formula RP-HSee Also: primary phosphine, tertiary phosphine
Wikipedia foundation.
Wikipedia foundation.
phosphine — /fos feen, fin/, n. Chem. 1. a colorless, poisonous, ill smelling, flammable gas, PH3. 2. any of certain organic derivatives of this compound. [1870 75; PHOSPH + INE1] * * * ▪ chemical compound (PH3),also called Hydrogen Phosphide, a… … Universalium
tertiary phosphine — noun any compound of general formula PR (where R is not H) See Also: primary phosphine, secondary phosphine … Wiktionary
primary phosphine — noun any compound of general formula R PH See Also: secondary phosphine, tertiary phosphine … Wiktionary
Organophosphorus — compounds are degradable organic compounds containing carbon–phosphorus bonds (thus excluding from phosphate and phosphite esters, which lack such kind of bonding), used primarily in pest control as an alternative to chlorinated hydrocarbons that … Wikipedia
Phosphorus — This article is about the chemical element. For other uses, see Phosphorus (disambiguation). silicon ← phosphorus → sulfur … Wikipedia
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Functional group — For other uses, see Functional group (disambiguation) and Moiety (disambiguation). Benzyl acetate has an ester functional group (in red), an acetyl moiety (circled with green) and a benzyloxy moiety (circled with orange). Other divisions can be… … Wikipedia
Disulfide bond — In chemistry, a disulfide bond (Br.E. disulphide bond) is a covalent bond, usually derived by the coupling of two thiol groups. The linkage is also called an SS bond or disulfide bridge. The overall connectivity is therefore R S S R. The… … Wikipedia
Hydroformylation — Hydroformylation, also known as oxo synthesis or oxo process, is an important industrial process for the production of aldehydes from alkenes.[1] This chemical reaction entails the addition of a formyl group (CHO) and a hydrogen atom to a carbon… … Wikipedia
Phenylphosphine — Other names … Wikipedia