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The bromination of triethylamine
Tetrahedron Letters, 1981Abstract The products of bromination of triethylamine have been reinvestigated and shown to be N.N-diethyl di- and tribromoacetamides. The rotational barrier for the dibromoamide was measured, Ea = 40 kJ mol−1 and found to be considerably lower than that of N,N-diethylacetamide.
Neil S. Isaacs +2 more
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Ultrasonic Relaxation in Triethylamine
Proceedings of the Physical Society, 1960The absorption of ultrasonic waves in triethylamine has been studied at temperatures between - 50°C and 25°C, at frequencies between 10 and 100 Mc/s. These measurements supplement those reported in 1956 by Heasell and Lamb and permit a more detailed analysis.
R A Padmanabhan, E L Heasell
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Triethylamine Trishydrofluoride in Synthesis
Journal f�r Praktische Chemie/Chemiker-Zeitung, 1996Triethylamine trishydrofluoride is a highly versatile fluorinating agent without the disadvantages of liquid hydrogen fluoride or other mixtures of HF with bases. The main types of fluorination using this reagent are reviewed: Nucleophilic substitutions, reactions using this reagent as nucleophilic partner in electrophilic additions ...
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Rotational isomerism in triethylamine
Chemical Physics Letters, 1971Abstract The vibrational spectrum of triethylamine was investigated which reveals the presence of at least two rotational isomers. These isomers are present in both the liquid and solid states. The TGG′ configuration is the more stable configuration in vapour phase.
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(Triethylamine)(pentacarbonyl)molybdenum
2002[33846-95-6] C11H15MoNO5 (MW 337.18) InChI = 1S/C6H15N.5CO.Mo/c1-4-7(5-2)6-3;5*1-2;/h4-6H2,1-3H3;;;;;; InChIKey = NEXLCCCSXFBZEZ-UHFFFAOYSA-N (catalyst for cycloisomerizations of terminal alkynyl alcohols, and other mechanistically related transformations of terminal alkynes1) Physical Data: for (Et3N)Mo(CO)5: λmax 393 ...
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