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Trimethylamine
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Trimethylamine (TMA) is an organic compound with the formula N(CH3)3. It is a trimethylated derivative of ammonia. TMA is widely used in industry. At higherArne Haaland (477 words) [view diff] case mismatch in snippet view article find links to article
phosphorus oxides P4O10 and P4O9, trimethylamuminium and its adducts with NMe3, and the first stable silylene. Haaland was the author of many contributionsTin(II) bromide (607 words) [view diff] case mismatch in snippet view article
trimethylamine where it forms NMe3·SnBr2 and 2NMe3·SnBr2 It can also act as both donor and acceptor in, for example, the complex F3B·SnBr2·NMe3 where it is a donorGallane (940 words) [view diff] case mismatch in snippet view article find links to article
ligand displacement from an existing adduct. Examples are: Ga2H6 + 2 NMe3 → (NMe3)2·GaH3 (-95°C) LiGaH4 + Me3NHCl → LiCl + H2+ Me3N·GaH3 Me2NH + Me3N·GaH3Vanadium(III) chloride (1,424 words) [view diff] case mismatch in snippet view article
ligands. This aspect is illustrated by the isolation of VCl3(NMe3)2, containing two bulky NMe3 ligands. Vanadium(III) chloride is able to form complexesNucleophilic abstraction (807 words) [view diff] case mismatch in snippet view article find links to article
pushes electrons on the metal. The reaction then proceeds to kick out CO2 and NMe3. An article from the Bulletin of Korean Chemical Society journal showed interestingTrimethylphosphine (548 words) [view diff] case mismatch in snippet view article find links to article
Flash point −19 °C (−2 °F; 254 K) Related compounds Related compounds PEt3 NMe3 PH3 PPh3 Except where otherwise noted, data are given for materials in theirMetal bis(trimethylsilyl)amides (3,034 words) [view diff] case mismatch in snippet view article
and V{N(SiMe3)2}3 are prepared using the soluble precursors TiCl3(NMe3)2 or VCl3(NMe3)2, respectively. The melting and boiling points of the complexesPhosphanide (1,895 words) [view diff] case mismatch in snippet view article find links to article
α=70.15° β=79.82° γ=68.78° NMe3•H2BPH2••W(CO)5 phosphanylalane NMe3•H2AlPH2•W(CO)5 cp(CO)2Fe(μ-PH2)W(CO)5 phosphanygallane NMe3•H2GaPH2••W(CO)5 Re2(μ-PH2)2(CO)8Tetramethylammonium hydroxide (1,345 words) [view diff] case mismatch in snippet view article find links to article
product rather than methanol. The idealized equation is: 2 NMe4+ OH− → 2 NMe3 + MeOMe + H2O TMAH is a very strong base. One of the industrial uses of TMAHVanadium compounds (1,842 words) [view diff] case mismatch in snippet view article find links to article
5-coordinate vanadyl complexes have a trigonal bipyramidal geometry, such as VOCl2(NMe3)2. The coordination chemistry of V5+ is dominated by the relatively stableVanadium (8,579 words) [view diff] case mismatch in snippet view article find links to article
5-coordinate vanadyl complexes have a trigonal bipyramidal geometry, such as VOCl2(NMe3)2. The coordination chemistry of V5+ is dominated by the relatively stablePhosphenium (1,948 words) [view diff] case mismatch in snippet view article find links to article
Valence orbital diagram of phosphenium (Left). Structure of model phosphenium (NMe3)P+ determined by X-ray crystallography (Right).Germanium(II) hydrides (2,198 words) [view diff] case mismatch in snippet view article
β-diketiminato germylene chloride was treated with the alane-amine adduct AlH3•NMe3 in toluene at -4 °C, the solution underwent a color change from yellow to