Five-fold plasmonic Fano resonances with giant bisignate circular dichroism

Nanoscale ◽  
2018 ◽  
Vol 10 (35) ◽  
pp. 16630-16637 ◽  
Author(s):  
Ximin Tian ◽  
Zhiguang Liu ◽  
Han Lin ◽  
Baohua Jia ◽  
Zhi-Yuan Li ◽  
...  

Chiral metamaterials with versatile designs can exhibit orders of magnitude enhancement in chiroptical responses compared with that of the natural chiral media.

2020 ◽  
Vol 13 (4) ◽  
pp. 722-727
Author(s):  
ZHU Ye-xin ◽  
◽  
◽  
LI Ya-nan ◽  
SHI Wei-jie ◽  
...  

Author(s):  
Furkan Dincer ◽  
Muharrem Karaaslan ◽  
Emin Unal ◽  
Mehmet Bakir ◽  
Utku Erdiven ◽  
...  

2020 ◽  
Vol 59 (12) ◽  
pp. 3686 ◽  
Author(s):  
Xiaoxiang Dong ◽  
Changji Liu ◽  
Yuanyuan Huang ◽  
Fangrong Hu ◽  
Yiwen E ◽  
...  

1971 ◽  
Vol 49 (4) ◽  
pp. 624-631 ◽  
Author(s):  
L. D. Hayward ◽  
R. N. Totty

In the presence of chiral environment compounds, C, optical rotation is induced in symmetric substrates, S, and may be detected as circular dichroism in the electronic spectra of the solutions. Thus the n − π* transitions of symmetric and racemic carbonyl compounds, and of symmetric nitro and azo compounds, become optically active when these S are dissolved in chiral hydrocarbons, ketones, or carbinols, or in solutions of these C in achiral solvents. The rotational strengths of the induced circular dichroism bands of S are solvent, temperature, and concentration dependent. Only limited correlation of the sign and magnitude of the induced bands with the stereochemistry of C and S is evident on the data so far accumulated. Halogenated achiral solvents enhance the intensity, and, in some cases reverse the sign of the induced bands.A new mechanism of asymmetric induction is proposed in which specific bonding of C with S is not prerequisite.


2012 ◽  
Vol 285 (10-11) ◽  
pp. 2750-2754 ◽  
Author(s):  
C. Feng ◽  
Z.B. Wang ◽  
S. Lee ◽  
J. Jiao ◽  
L. Li

2020 ◽  
Vol 532 (7) ◽  
pp. 2000065 ◽  
Author(s):  
Fuyu Li ◽  
Tingting Tang ◽  
Yinghui Mao ◽  
Li Luo ◽  
Jie Li ◽  
...  

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