Circular electrodichroism of light in isotropic optically active media

JETP Letters ◽  
1997 ◽  
Vol 66 (8) ◽  
pp. 549-554 ◽  
Author(s):  
N. I. Koroteev
Keyword(s):  
Optically Active ◽  
Active Media

Surface Plasmon-Polariton Terahertz Waves in Optically Active Media

2010 ◽  
Vol 5 (4) ◽  
pp. 154-157
Author(s):  
Anatoliy P. Sukhorukov ◽  
Darya O. Saparina ◽  
Andrey N. Kalish
Keyword(s):  
Active Medium ◽  
Surface Plasmon ◽  
Surface Plasmon Polariton ◽  
Optically Active ◽  
Wave Profile ◽  
Terahertz Waves ◽  
Localized Modes ◽  
Nonlinear Dielectric ◽  
Active Media ◽  
Plasmon Polariton

We examine the propagation of surface plasmon-polariton terahertz waves along the interface between two media: metal or metamaterial with a negative index and an optically active medium or a nonlinear dielectric. It is shown that in both cases wave profile is not exponential. On the interface of optically active media surface waves are combination of TE and TM localized modes. Diffraction and dispersion of terahertz beams and pulses is studied

Frequency conversion light waves in optically active media

1970 ◽  
Vol 12 (1) ◽  
pp. 55-60 ◽  
Author(s):  
B. V. Bokut' ◽  
A. N. Serdyukov
Keyword(s):  
Frequency Conversion ◽  
Optically Active ◽  
Active Media ◽  
Light Waves

THE REDUCTION, ENOLATE FORMATION, AND SOLVOLYSIS OF GRIGNARD REAGENTS IN OPTICALLY ACTIVE MEDIA

1957 ◽  
Vol 35 (8) ◽  
pp. 900-910 ◽  
Author(s):  
Norman Allentoff ◽  
George F Wright
Keyword(s):  
Grignard Reagent ◽  
Optically Active ◽  
Grignard Reagents ◽  
Inactive State ◽  
Active Media

The sec-butylbenzene produced by solvolysis of 2-phenyl-2-chlorobutane Grignard reagent in (+) 2,3-dimethoxybutane and benzene is optically inactive. The 2-↓-isopropyl-4-↑-methylcyclohexanols obtained by the reducing action of isopropyl Grignard reagent on racemic 2-↓-isopropyl-4-↑-methylcyclohexanone in (+) dimethoxybutane are optically active to the extent of 6 and 15%. The bromomagnesium enolates obtained by the action of isopropyl Grignard reagent on racemic 2-↓-isopropyl-4-↑-methylcyclohexanone in (+) dimethoxybutane regenerate the parent ketone in an optically inactive state but the diastereomeric 2-↑-isopropyl-4-↑-methylcyclohexanone also produced is optically active to the extent of about 6%.

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