Aromatic compound light absorption

Armstrong and Boalch [60] have examined the ultraviolet absorption of seawater, particularly in the wavelengths between 250 and 300 nm, where the absorption is considered to result from the presence of aromatic compounds. Light absorption is a particularly useful measure, if it can be made to work, since it is not too difficult to construct an in situ colorimeter which can produce continuous profiles of dissolved organic carbon with distance or depth [71]. 

In addition to these two primary processes, there are also possibilities of sensitization of the photooxidation by a variety of mechanisms. The first of these is the formation of an excited state of a ketone or a polynuclear aromatic compound by absorption of light followed by quenching with oxygen to form singlet oxygen (102) which later adds to a double bond in the polymer to form an allylic hydroperoxide by the scheme shown below. This reaction has been demonstrated to occur quantitatively in... 

We have limited our investigations to the action of gamma-rays and fast neutrons on aromatic, alicyclic, aliphatic, and ionic compounds. The absorption coefficients for these types of radiation have an order of magnitude of lO /cm which is particularly adequate. Shallow penetrating radiations would only alter the superficial layers and would obviously not be able to affect the intensity of the quadrupole line substantially. This is for instance the case for ultraviolet light which has been shown to be unable to produce any effect on the resonance line of iodoform (CHI3 3Sg)... 

In the laser photolysis experiments the aromatic compound (4-10" M) and the nucleophile (0 04 M ) in acetonitrile-water (1 1) were irradiated with the frequency doubled pulse (100 mj, 6 ns, 347 nm) of a ruby laser. Only time-dependent absorption changes were measured (double pulsed xenon flash lamp with 10 /is continuous output as light source) absorption spectra were constructed from these measurements at 12 or 25 nm intervals. 

It is well known that cyano derivatives of anthracene form charge transfer (CT) complexes with certain aromatic compounds. It was reported [67] that the radical cations formed upon irradiation of these complexes played an important role in initiation of cationic polymerization of cyclic ethers. Pyridinium salts were also found [68] to form CT complexes with hexamethyl benzene and trimethoxy benzene which result in the formation of a new absorption band at longer wavelengths where both donor and acceptor molecules have no absorption. This way the light sensitivity of the pyridinium salts may be extended towards the visible range. According to the results obtained from the... 

Figure 27. Application of flow cell and UV spectroscopy to study the reduction of aromatic compounds in iV,iV-dimethylformamide/0.1 M BU4NBF4 a) Plot of absorbance at = 556 nm and 732 nm, of the products obtained in the reduction of anthraquinone (T) and anthracene ( ), respectively, as the galvanostatic current to the flow cell is increased and a continuous flow of 5 mL min is maintained. The substrate concentrations are both 0.1 mM and the light path is 1 cm b) and c) The absorption spectra of the product obtained from reduction of anthraquinone and anthracene, respectively, when the galvanostatic current is increased above the maximum required for generating the radical anion. The current is increased from 2.0 to 2.8 mA in steps of 0.2 mA and the development in the spectra is indicated with arrows. Isosbestic points are also indicated. For anthraquinone, the spectra of the radical anion and the dianion could be resolved whereas for anthracene the dianion is protonated and spectra of the radical anion and 9,10-dihydroanthracen-9-ide could be resolved [65].

The formation of HRP-substrate compounds shifts the CD and light-absorption bands in the Soret region in a similar fashion. Differences observed in the CD near 280 nm between the enzyme and the enzyme-substrate complex could reflect changes in orientation of aromatic amino acid residues upon binding, provided the heme does not contribute to the CD in this region (258). 

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