1991
DOI: 10.1021/j100162a014
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Infrared matrix isolation study of the reaction of diborane with the methylamines

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Cited by 33 publications
(25 citation statements)
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“…Based on the analogous chemistry for 1, 3 and 5 a plausible intermediate in the conversion of 2 to 8 is methylaminoborane, MeNHQBH 2 , 9. This species, the B-N analog of propylene, is highly reactive and has only previously been detected by IR spectroscopy in inert gas matrices at 14 K. 15 Trapping of this species is possible with cyclohexene, as shown in previous thermal and catalytic redistribution reactions of linear diborazanes. 10c To test for the presence of 9 as an intermediate, 2.5 equiv.…”
mentioning
confidence: 87%
“…Based on the analogous chemistry for 1, 3 and 5 a plausible intermediate in the conversion of 2 to 8 is methylaminoborane, MeNHQBH 2 , 9. This species, the B-N analog of propylene, is highly reactive and has only previously been detected by IR spectroscopy in inert gas matrices at 14 K. 15 Trapping of this species is possible with cyclohexene, as shown in previous thermal and catalytic redistribution reactions of linear diborazanes. 10c To test for the presence of 9 as an intermediate, 2.5 equiv.…”
mentioning
confidence: 87%
“…[16][17][18][19][20] Investigations of transient boron species using the matrixisolation technique have been reported. [21][22][23][24][25] For instance, reactions of H 2 with boron atoms evaporated with a pulsed laser and condensed in excess argon at 10 K yielded products such as BH, (H 2 )(BH) complex, BH 3 , (H 2 )(BH 3 ) complex, HBBH and B 2 H 6 , identied from infrared absorption spectra. 23 The irradiation of samples of B 2 H 6 diluted in neon or argon at 4 K with light at 16.8 eV followed by X-rays and electrons at 50 eV enabled the detection of BH 2 , BO, B 2 and HBBH through electron-paramagnetic-resonance spectra, 24 but no neutral boron hydride species with less than six H atoms and a bridging B-H-B bond has been experimentally identied before our work.…”
Section: Introductionmentioning
confidence: 99%
“…In both cases 3,4 , amino borane (BH 2 NH 2 ) and borazine (B 3 N 3 H 6 ) were observed as gas phase products with mass spectrometry. Miranda There have been previous relevant IR studies of ammonia borane 6,7 and of amino borane in the gas 8 and solid 9 phases, or trapped in inert matrices [10][11][12] . The loss of hydrogen to form amino borane-like structures with a B=N double bond should be apparent in the IR spectra.…”
Section: Introductionmentioning
confidence: 99%