Research output: Contribution to journal › Article › peer-review
Raman spectra of deuterated hydrocarbons for labeling applications. / Okotrub, Konstantin A.; Shamaeva, Daria V.; Surovtsev, Nikolay V.
In: Journal of Raman Spectroscopy, Vol. 53, No. 2, 02.2022, p. 297-309.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Raman spectra of deuterated hydrocarbons for labeling applications
AU - Okotrub, Konstantin A.
AU - Shamaeva, Daria V.
AU - Surovtsev, Nikolay V.
N1 - Funding Information: This work was supported by Russian Science Foundation (Grant No. 19‐74‐00050). Raman experiments were performed in the Multiple‐access center “High resolution spectroscopy of gases and condensed matters” in IA&E SB RAS (Novosibirsk, Russia). Publisher Copyright: © 2021 John Wiley & Sons, Ltd.
PY - 2022/2
Y1 - 2022/2
N2 - Raman spectroscopy is used for studying the composition of cell lipidome. However, the Raman approach suffers from limited distinguish power for different lipids. In recent years, isotopically labeled molecules are increasingly used to enhance the Raman resolution of similar compounds in biological samples. Here, we present Raman study of fully deuterated stearic acid (stearic-d35), semi-deuterated oleic acid (oleic d-9), arachidonic acid with deuterated methine groups (arachidonic-d8), and their hydrogenated analogs. Polarization properties and temperature dependences of CD stretching modes were investigated to reveal the capability of the isotopically shifted Raman peaks in molecular characterization. Sensitivity of Raman peaks to order–disorder transition corresponding was demonstrated for deuterated methine, methylene, and methyl groups. It was found that the isotopically shifted Raman peaks provide information about the orientation of deuterated Raman tags and their surroundings.
AB - Raman spectroscopy is used for studying the composition of cell lipidome. However, the Raman approach suffers from limited distinguish power for different lipids. In recent years, isotopically labeled molecules are increasingly used to enhance the Raman resolution of similar compounds in biological samples. Here, we present Raman study of fully deuterated stearic acid (stearic-d35), semi-deuterated oleic acid (oleic d-9), arachidonic acid with deuterated methine groups (arachidonic-d8), and their hydrogenated analogs. Polarization properties and temperature dependences of CD stretching modes were investigated to reveal the capability of the isotopically shifted Raman peaks in molecular characterization. Sensitivity of Raman peaks to order–disorder transition corresponding was demonstrated for deuterated methine, methylene, and methyl groups. It was found that the isotopically shifted Raman peaks provide information about the orientation of deuterated Raman tags and their surroundings.
KW - arachidonic acid
KW - deuteration
KW - oleic acid
KW - Raman spectroscopy
KW - stearic acid
UR - http://www.scopus.com/inward/record.url?scp=85119009984&partnerID=8YFLogxK
U2 - 10.1002/jrs.6279
DO - 10.1002/jrs.6279
M3 - Article
AN - SCOPUS:85119009984
VL - 53
SP - 297
EP - 309
JO - Journal of Raman Spectroscopy
JF - Journal of Raman Spectroscopy
SN - 0377-0486
IS - 2
ER -
ID: 34642716