Raman spectrum detection method of phenylalanine enantiomer
A technology of Raman spectrum detection and phenylalanine, which is applied in the field of spectral analysis and chiral recognition, can solve the problems of inability to distinguish enantiomers and achieve good accuracy
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Embodiment 1
[0028] 1) Preparation of gold seed solution: HAuCl 4 The solution was mixed with a cetyltrimethylammonium bromide (CTAB) solution, and a freshly prepared sodium borohydride solution was added, stirred rapidly for 2 minutes, and left to stand at 30°C for 2 hours to obtain a gold seed solution;
[0029] 2) Preparation of gold growth solution: add HAuCl in CTAB solution sequentially 4 , AgNO 3 And freshly configured ascorbic acid solution, the solution turns from bright yellow to colorless and transparent;
[0030] 3) Preparation of gold nanorods: adding the above gold seed solution into the gold growth solution, reacting at room temperature for 24 hours, centrifuging, and then dispersing the obtained precipitate in water to obtain gold nanorods;
[0031] 4) Preparation of Au / Ag nanorods: Add CTAB to the above gold nanorod dispersion solution and mix evenly, then add 10 μL AgNO 3 solution (100mmol / L) and the corresponding fourfold volume of ascorbic acid solution (100mmol / L), ...
Embodiment 2
[0039] D-Phe or L-Phe solution (concentration is 6.7×10 -6 mol / L) was dropped on a flat aluminum foil, and then the Raman spectrum was measured on a Raman spectrometer equipped with a 785nm laser, and it was found that the characteristic Raman scattering signal of D-Phe or L-Phe could not be detected.
Embodiment 3
[0041] This embodiment is basically the same as embodiment 1, but in step 4) AgNO 3 The volume of the solution (100 mmol / L) was 0 μL (ie to prepare gold nanorods), and it was found that the Raman scattering signal of D-Phe or L-Phe could not be detected by using gold nanorods alone.
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