About: Diphosgene is a research topic. Over the lifetime, 159 publications have been published within this topic receiving 1203 citations. The topic is also known as: trichloromethyl chloroformate.
TL;DR: Methyl 1,1,1-trichloromethyl carbonate was synthesized and characterized also by the APCI-MS technique, and the experimental data suggest that the maximum concentration of phosgene during the methanolysis of triphos gene was lower than 1 x 10(-)(5) M.
Abstract: Triphosgene was decomposed quantitatively to phosgene by chloride ion. The reaction course was monitored by IR spectroscopy (React-IR), showing that diphosgene was an intermediate. The methanolysis of triphosgene in deuterated chloroform, monitored by proton NMR spectroscopy, gave methyl chloroformate and methyl 1,1, 1-trichloromethyl carbonate in about a 1:1 ratio, as primary products. The reaction carried out in the presence of large excess of methanol (0.3 M, 30 equiv) was a pseudo-first-order process with a k(obs) of 1.0 x 10(-)(4) s(-)(1). Under the same conditions, values of k(obs) of 0.9 x 10(-)(3) s(-)(1) and 1.7 x 10(-)(2) s(-)(1) for the methanolysis of diphosgene and phosgene, respectively, were determined. The experimental data suggest that, under these conditions, the maximum concentration of phosgene during the methanolysis of triphosgene and diphosgene was lower than 1 x 10(-)(5) M. Methyl 1,1,1-trichloromethyl carbonate was synthesized and characterized also by the APCI-MS technique.
TL;DR: Polymerisation en solution de diacides carboxylique en presence de phosgene a temperature ambiante as mentioned in this paper is a common technique for diacide synthesis.
Abstract: Polymerisation en solution de diacides carboxylique en presence de phosgene a temperature ambiante
TL;DR: A new 1,8-naphthalimide-based fluorescent chemosensor, Phos-2, which exhibits high sensitivity, high selectivity to phosgene and its substitutes over nitric oxide (NO), various acyl chlorides, and nerve agent mimics in solutions is developed.
Abstract: Phosgene and its substitutes, diphosgene and triphosgene, are highly toxic and widely used chemicals, so it is necessary to investigate their reactivity and develop facile, sensitive, and specific methods for detecting them. In this work, we have developed a new 1,8-naphthalimide-based fluorescent chemosensor, Phos-2, which exhibits high sensitivity (detection limits: 0.2-0.7 nm), high selectivity to phosgene and its substitutes over nitric oxide (NO), various acyl chlorides, and nerve agent mimics in solutions. Based on investigation of the reaction kinetics of Phos-2 with phosgene and its substitutes, a two-step sensing mechanism was clarified. The second-order rate constants (k2 ) of Phos-2 reveal that the relative rate constants of phosgene, diphosgene, and triphosgene are 40:4:1. Moreover, a Phos-2 test paper has been fabricated as a low-cost, sensitive (≈5 ppm from observation by the naked eye or 0.1 ppm from a measurement), and efficient method for visual detection of a low concentration of phosgene in the gas phase.
TL;DR: In this article, 11 enamides were prepared by adopting different procedures, including POCl3/DMF, diphosgene, triphosgenes, and triphoSgene/DMFs, leading to the formation of various multisubstituted chloronicotinaldehydes.