Organic molecules absorption spectrum

To verify effectiveness of NDCPA we carried out the calculations of absorption spectra for a system of excitons locally and linearly coupled to Einstein phonons at zero temperature in cubic crystal with one molecule per unit cell (probably the simplest model of exciton-phonon system of organic crystals). Absorption spectrum is defined as an imaginary part of one-exciton Green s function taken at zero value of exciton momentum vector... 

In Pedersen s early experiments, the relative binding of cations by crown ethers was assessed by extraction of alkali metal picrates into an organic phase. In these experiments, the crown ether served to draw into the organic phase a colored molecule which was ordinarily insoluble in this medium. An extension and elaboration of this notion has been developed by Dix and Vdgtle and Nakamura, Takagi, and Ueno In efforts by both of these groups, crown ether molecules were appended to chromophoric or colored residues. Ion-selective extraction and interaction with the crown and/or chromophore could produce changes in the absorption spectrum. Examples of molecules so constructed are illustrated below as 7 7 and 18 from refs. 32 and 131, respectively. 

Absorption spectrum (Section 12.5) A plot of wavelength of incident light versus amount of light absorbed. Organic molecules show absorption spectra in both the infrared and the ultraviolet regions of the electromagnetic spectrum. 

Absorption of ultraviolet and visible radiation in organic molecules is restricted to certain functional groups (chromophores) that contain valence electrons of low excitation energy (Figure 4). The spectrum of a molecule containing these chromophores is complex. This is because the superposition of rotational and vibrational transitions on the electronic transitions gives a combination of overlapping lines. This appears as a continuous absorption band. 

There are also a number of powerful NMR experiments that yield detailed information about the structure of pure organic molecules. However, as with other regions of the spectrum (see Figure 14.4), chemical mixtures produce spectra that are combinations of all of the absorption features of all of the components in the mixture. The H NMR spectrum of a mixture of toluene, hexanoic acid, and octanal is shown in Figure 14.6. This spectrum shows the unique absorptions of each of these functional groups and also illustrates that mixtures of compounds give spectra containing the absorption bands of all the components. If an impure sample had such a spectrum, it would not be known... 

Fig. 8 Kubelka-Munk optical absorption spectra of as-prepared mesostructured (black) and mesoporous NU-Ge-1 (red) semiconductors and NU-Ge-1 incorporating into the pores TCNE (blue) and TTF (green line) organic molecules. The recovered optical adsorption spectra of NU-Ge-1 by encapsulation of TCNE-TTF complexes are also given (dashed lines). Inset optical absorption spectrum of NU-Ge-1 encapsulating anthracene...

Infrared radiation of frequencies less than about 100 cm-1 is absorbed and converted by an organic molecule into energy of molecular rotation. This absorption is quantized thus a molecular rotation spectrum consists of discrete lines. 

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