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  2. Phosgene - Wikipedia

    en.wikipedia.org/wiki/Phosgene

    Phosgene is an organic chemical compound with the formula COCl 2. It is a toxic, colorless gas; in low concentrations, its musty odor resembles that of freshly cut ...

  3. Phosphine - Wikipedia

    en.wikipedia.org/wiki/Phosphine

    Phosphine (IUPAC name: phosphane) is a colorless, flammable, highly toxic compound with the chemical formula P H 3, classed as a pnictogen hydride. Pure phosphine is odorless, but technical grade samples have a highly unpleasant odor like rotting fish, due to the presence of substituted phosphine and diphosphane ( P 2 H 4 ).

  4. Chemical weapons in World War I - Wikipedia

    en.wikipedia.org/wiki/Chemical_weapons_in_World...

    German phosgene came in the form of diphosgene, codenamed Grün Kreuz (Green cross). This was less effective than its allied counterpart, being less toxic and slower to evaporate, but was easier to handle in shell manufacture early in the war. [35] Phosgene was a potent killing agent, deadlier than chlorine.

  5. Category:Phosphines - Wikipedia

    en.wikipedia.org/wiki/Category:Phosphines

    Phosphines or phosphanes are phosphorus compounds derived from phosphine and have the general structure R 3 P. For the nitrogen analogues, please see Category:Inorganic amines . Wikimedia Commons has media related to Phosphines .

  6. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    Compounds related to phosphine oxides include phosphine imides (R 3 PNR') and related chalcogenides (R 3 PE, where E = S, Se, Te). These compounds are some of the most thermally stable organophosphorus compounds. In general, they are less basic than the corresponding phosphine oxides, which can adduce to thiophosphoryl halides: [7]: 73

  7. Organophosphine - Wikipedia

    en.wikipedia.org/wiki/Organophosphine

    The reaction with oxygen is spin-forbidden but still proceeds at sufficient rate that samples of tertiary phosphines are characteristically contaminated with phosphine oxides. Qualitatively, the rates of oxidation are higher for trialkyl vs triarylphosphines. Faster still are oxidations using hydrogen peroxide. Primary and secondary phosphines ...

  8. Dying To Be Free - The Huffington Post

    projects.huffingtonpost.com/dying-to-be-free...

    That day, in August 2013, Patrick got in the car and put the duffel bag on a seat. Inside was a talisman he’d been given by the treatment facility: a hardcover fourth edition of the Alcoholics Anonymous bible known as “The Big Book.”

  9. Green Cross (chemical warfare) - Wikipedia

    en.wikipedia.org/wiki/Green_Cross_(chemical_warfare)

    Green Cross (Grünkreuz) is a World War I chemical warfare pulmonary agent consisting of chloropicrin (PS, Aquinite, Klop), phosgene (CG, Collongite) and/or trichloromethyl chloroformate (Surpalite, Perstoff). Green Cross is also a generic World War I German marking for artillery shells with pulmonary agents (chemical payload affecting the ...