scholarly journals Interaction of cyanlne dyes with nucleic acids. 9. The study of spectral properties of cyanine dyes-DNA complexes in the presence of organic solvents

2000 ◽  
Vol 16 (1) ◽  
pp. 75-81 ◽  
Author(s):  
M. Yu. Losytskyy ◽  
V. B. Kovalska ◽  
S. M. Yarmoluk
2011 ◽  
Vol 222 ◽  
pp. 271-274 ◽  
Author(s):  
Elmars Zarins ◽  
Janis Jubels ◽  
Valdis Kokars

New organic glassy non symmetric styryl- derivatives of 2(2,6-substituted-4H-pyran-4-ylidene)-malononitrile, 2(2,6-substituted-4H-pyran-4-ylidene)-1H-indene-1,3(2H)-dione and 2(2,6-substituted-4H-pyran-4-ylidene)-pyrimidine-2,4,6(1H,3H,5H)-trione were synthesized. They form thin solid amorphous films from volatile organic solvents (DCM and chloroform). Their spectral properties have been studied.


In a previous investigation of the absorption spectra and sensitising properties of some iso cyanine dyes,* the influence of the solvent was examined and it was found that the absorption maximum was shifted toward the red as the refractive index of the solvent increased. This is in accordance with Kundt’s law. The absorption in water, however, differs markedly from that in organic solvents. In the latter the spectrum consists of a prominent band in the orange and a half-shade nearer the blue. In water this half-shade has become a separate band comparable in intensity with the orange. Absorption curves in alcohol and water are shown. It is convenient to term the band near the red the β-(organic) band, the one nearer the blue the α -(water) band. It appeared desirable to investigate this difference further.


2009 ◽  
Vol 82 (3) ◽  
pp. 409-415 ◽  
Author(s):  
Yi-Le Fu ◽  
Wei Huang ◽  
Chun-Lan Li ◽  
Lan-Ying Wang ◽  
Yong-Sheng Wei ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document