Surface-Enhanced Hyper-Raman Spectra of Adenine, Guanine, Cytosine, Thymine, and Uracil

被引:160
|
作者
Madzharova, Fani [1 ]
Heiner, Zsuzsanna [1 ,2 ]
Guehlke, Marina [1 ]
Kneipp, Janina [1 ,2 ]
机构
[1] Humboldt Univ, Dept Chem, Brook Taylor Str 2, D-12489 Berlin, Germany
[2] Humboldt Univ, Sch Analyt Sci Adlershof SALSA, Albert Einstein Str 5-11, D-12489 Berlin, Germany
来源
Journal of Physical Chemistry C | 2016年 / 120卷 / 28期
关键词
DENSITY-FUNCTIONAL THEORY; SILVER NANOPARTICLE SURFACES; RESONANCE RAMAN; THEORETICAL DFT; GOLD SOLS; SCATTERING; SPECTROSCOPY; DERIVATIVES; PYRIDINE; SERS;
D O I
10.1021/acs.jpcc.6b02753
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Using picosecond excitation at 1064 nm, surface enhanced hyper-Raman scattering (SEHRS) spectra of the nucleobases adenine, guanine, cytosine, thymine, and uracil with two different types of silver nanoparticles were obtained. Comparing the SEHRS spectra with SERS data from the identical samples excited at 532 nm and with known infrared spectra, the major bands in the spectra are assigned. Due to the different selection rules for the one- and two-photon excited Raman scattering, we observe strong variation in relative signal strengths of many molecular vibrations obtained in SEHRS and SERS spectra. The two-photon excited spectra of the nucleobases are found to be very sensitive with respect to molecule nanoparticle interactions. Using both the SEHRS and SERS data, a comprehensive vibrational characterization of the interaction of nucleobases with silver nanostructures can be achieved.
引用
收藏
页码:15415 / 15423
页数:9
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