1957
DOI: 10.1021/jo01353a032
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Infrared Spectra of Allenic Compounds

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1967
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Cited by 73 publications
(22 citation statements)
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“…The major spectroscopic change is the appearance of a new peak at 1921 cm -1 , ascribed to the characteristic vibration of a CdCdC skeleton (asymmetric stretching mode). [18][19][20] This assignment is further supported by the concurrent observation of its torsion (846 cm -1 ) and bending (361 cm -1 ) modes. Furthermore, the two new peaks at 626 and 714 cm -1 are ascribed to the Si-C and Si-O stretching modes, 11,21 respectively.…”
Section: Iiia High-resolution Electron Energy Loss Spectroscopymentioning
confidence: 66%
“…The major spectroscopic change is the appearance of a new peak at 1921 cm -1 , ascribed to the characteristic vibration of a CdCdC skeleton (asymmetric stretching mode). [18][19][20] This assignment is further supported by the concurrent observation of its torsion (846 cm -1 ) and bending (361 cm -1 ) modes. Furthermore, the two new peaks at 626 and 714 cm -1 are ascribed to the Si-C and Si-O stretching modes, 11,21 respectively.…”
Section: Iiia High-resolution Electron Energy Loss Spectroscopymentioning
confidence: 66%
“…Im Infrarot besitzt 3 bei 5,06 ,u eine typische Allenbande (vgl. [7]). Auch das Phenylsemicarbazon von 3, Smp.…”
Section: Uber Eine Neuartige Synthese Von P-ketoallenen Durch Reaktiounclassified
“…[18] This characteristic signal is observed as a sharp band at 2150 cm À1 for allene 13. [18] This characteristic signal is observed as a sharp band at 2150 cm À1 for allene 13.…”
Section: Mathieu Leclre and Alex G Fallis*mentioning
confidence: 96%
“…Allenic compounds usually display a unique antisymmetrical C = C = C IR stretching band in the region of 1950-2150 cm À1 . [18] This characteristic signal is observed as a sharp band at 2150 cm À1 for allene 13. We were initially surprised to observe no distinct corresponding band for macrocycle 3.…”
Section: Mathieu Leclre and Alex G Fallis*mentioning
confidence: 96%