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Acetonitrile

About: Acetonitrile is a research topic. Over the lifetime, 11298 publications have been published within this topic receiving 175275 citations. The topic is also known as: cyanomethane & ethyl nitrile.


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Journal ArticleDOI
TL;DR: The addition of an organic acid (formic, acetic or trifluoroacetic acid) was found to strongly influence the retention of the basic amino drugs in these nonaqueous systems and had deep impact on enantioresolution.

64 citations

Journal ArticleDOI
TL;DR: In this article, an ionization reagent for the location of double bonds in monoenes was proposed for the identification of insect pheromones, which is highly sensitive to a range of functional groups by isolating [C3H4N]+ from the other acetonitrile ions before reaction with the alkene.
Abstract: Acetonitrile may be used as a chemical ionization reagent gas in ion-trap mass spectrometry for the location of double bonds in functionalized long-chain monoenes. [C3H4N]+, derived from acetonitrile, reacts with carbon–carbon double bonds, generating one or a pair of fragment ions characteristic of the position of the double bond in the chain. Tolerance of a range of functional groups is achieved by isolating [C3H4N]+ from the other acetonitrile ions before reaction with the alkene. Under these conditions, competing processes such as protonation are minimized, and a different mode of fragmentation from that previously observed with unfunctionalized alkenes11 is obtained. The technique is highly sensitive (<0.5 ng), allowing its use in the identification of insect pheromones. Copyright © 1999 John Wiley & Sons, Ltd.

64 citations

Journal ArticleDOI
TL;DR: In this paper, three packings with the following surface composition were synthesized on LiChrosorb Si 100, d p  10 μm: [Cu(II) 3-(L -prolyl)propyl] + (packing I), [cu(II] 3-( L -hydroxyprolylpyl) propyl]+ (packing II) and [cu[2] 3-propyl spacer of the bonded ligand, etc., with remaining excess 3-iodopropyl groups (packing III).

63 citations

Journal ArticleDOI
TL;DR: The photosubstitution (electron transfer) reaction between 1,4-dicyanobenzene (1) and 2,3-dimethyl-2-butene (2) as discussed by the authors gave 1-(4-cyanophenyl)-2,3 -dimethyl 2-butenes (3) and 3-(4]-cyan-phenyl 2-3-di...
Abstract: The photosubstitution (electron transfer) reaction between 1,4-dicyanobenzene (1) and 2,3-dimethyl-2-butene (2), which gives 1-(4-cyanophenyl)-2,3-dimethyl-2-butene (3) and 3-(4-cyanophenyl)-2,3-di...

63 citations

Journal ArticleDOI
TL;DR: Ruthenium(II) phthalocyanine complexes of the type RuPcL2 (Pc = the phhalocyaninato dianion, L = various pyridines, imidazole, dimethylformamide, and acetonitrile) may be prepar...
Abstract: Ruthenium(II) phthalocyanine complexes of the type RuPcL2 (Pc = the phthalocyaninato dianion, L = various pyridines, imidazole, dimethylformamide, dimethylsulfoxide, and acetonitrile) may be prepar...

63 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023533
20221,074
2021178
2020172
2019229
2018207