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Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates.

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Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates. / Davies, J. Eric D.; Lie Ken Jie, Marcel S. F.; Bakare, Oladapo.
In: Chemistry and Physics of Lipids, Vol. 85, No. 2, 28.02.1997, p. 175-180.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Davies, JED, Lie Ken Jie, MSF & Bakare, O 1997, 'Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates.', Chemistry and Physics of Lipids, vol. 85, no. 2, pp. 175-180. https://doi.org/10.1016/S0009-3084(96)02647-3

APA

Davies, J. E. D., Lie Ken Jie, M. S. F., & Bakare, O. (1997). Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates. Chemistry and Physics of Lipids, 85(2), 175-180. https://doi.org/10.1016/S0009-3084(96)02647-3

Vancouver

Davies JED, Lie Ken Jie MSF, Bakare O. Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates. Chemistry and Physics of Lipids. 1997 Feb 28;85(2):175-180. doi: 10.1016/S0009-3084(96)02647-3

Author

Davies, J. Eric D. ; Lie Ken Jie, Marcel S. F. ; Bakare, Oladapo. / Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates. In: Chemistry and Physics of Lipids. 1997 ; Vol. 85, No. 2. pp. 175-180.

Bibtex

@article{de35c47e7340426f88deb02382734cdb,
title = "Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates.",
abstract = "Raman spectra (300–1200 cm−1) have been recorded for all the positional isomers of the selena (X=Se), sulphinyl (X=SO) and sulphonyl (X=SO2) methyl laurates CH3(CH2)nX(CH2)mCO2CH3, (n+m =9). The Raman spectra of two isomers of the tellura series (X=Te) were also obtained as were the IR spectra of the sulphonyl series. The SeC2 and TeC2 moieties each give two characteristic Raman bands at 564 and 651 cm−1 and 510 and 600 cm−1 respectively. The SO group gives a characteristic Raman band at 1016 cm−1. The symmetric stretching and bending modes of the SO2 group can be observed in both the IR and Raman spectra at 1109 and 517 cm−1 respectively. These quoted values do change when the functional group is near the carbonyl group or towards the end of the alkyl chain",
keywords = "Raman spectroscopy, IR spectroscopy, Selenalaurates, Telluralaurates, Sulphinyl laurates, Sulphonyl laurates",
author = "Davies, {J. Eric D.} and {Lie Ken Jie}, {Marcel S. F.} and Oladapo Bakare",
year = "1997",
month = feb,
day = "28",
doi = "10.1016/S0009-3084(96)02647-3",
language = "English",
volume = "85",
pages = "175--180",
journal = "Chemistry and Physics of Lipids",
issn = "0009-3084",
publisher = "Elsevier Ireland Ltd",
number = "2",

}

RIS

TY - JOUR

T1 - Raman and infrared spectral studies of selena, sulphinyl, sulphonyl and tellura methyl laurates.

AU - Davies, J. Eric D.

AU - Lie Ken Jie, Marcel S. F.

AU - Bakare, Oladapo

PY - 1997/2/28

Y1 - 1997/2/28

N2 - Raman spectra (300–1200 cm−1) have been recorded for all the positional isomers of the selena (X=Se), sulphinyl (X=SO) and sulphonyl (X=SO2) methyl laurates CH3(CH2)nX(CH2)mCO2CH3, (n+m =9). The Raman spectra of two isomers of the tellura series (X=Te) were also obtained as were the IR spectra of the sulphonyl series. The SeC2 and TeC2 moieties each give two characteristic Raman bands at 564 and 651 cm−1 and 510 and 600 cm−1 respectively. The SO group gives a characteristic Raman band at 1016 cm−1. The symmetric stretching and bending modes of the SO2 group can be observed in both the IR and Raman spectra at 1109 and 517 cm−1 respectively. These quoted values do change when the functional group is near the carbonyl group or towards the end of the alkyl chain

AB - Raman spectra (300–1200 cm−1) have been recorded for all the positional isomers of the selena (X=Se), sulphinyl (X=SO) and sulphonyl (X=SO2) methyl laurates CH3(CH2)nX(CH2)mCO2CH3, (n+m =9). The Raman spectra of two isomers of the tellura series (X=Te) were also obtained as were the IR spectra of the sulphonyl series. The SeC2 and TeC2 moieties each give two characteristic Raman bands at 564 and 651 cm−1 and 510 and 600 cm−1 respectively. The SO group gives a characteristic Raman band at 1016 cm−1. The symmetric stretching and bending modes of the SO2 group can be observed in both the IR and Raman spectra at 1109 and 517 cm−1 respectively. These quoted values do change when the functional group is near the carbonyl group or towards the end of the alkyl chain

KW - Raman spectroscopy

KW - IR spectroscopy

KW - Selenalaurates

KW - Telluralaurates

KW - Sulphinyl laurates

KW - Sulphonyl laurates

U2 - 10.1016/S0009-3084(96)02647-3

DO - 10.1016/S0009-3084(96)02647-3

M3 - Journal article

VL - 85

SP - 175

EP - 180

JO - Chemistry and Physics of Lipids

JF - Chemistry and Physics of Lipids

SN - 0009-3084

IS - 2

ER -