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The action of ultra violet rays of 260 nm on aqueous solutions of bases, nucleosides and nucleotides of DNA at 77°K is studied by electron spin resonance. It is shown that the free radicals observed are similar, with a few noteworthy exceptions to those induced by X-rays, under the same conditions of temperature, in the solid state. Contrary to what might be excepted on the basis of the results obtained by X-rays, the variation in the yield in paramagnetic centres in each sequence studied does not seem to be important. 相似文献
3.
ALBERT VAN DE VORST 《Photochemistry and photobiology》1971,13(4):321-336
Abstract— –The photosensitization of amino acids by proflavine is studied using the technique of electron spin resonance spectroscopy. The analysis of the line shape as a function of the incident microwave power (both in the presence and absence of oxygen) and the dependence of the numbers of free radicals on the intensity of the incident light allow one to suggest that two types of radicals are formed. One is formed by a biphotonic process, the nature of the radicals being the same as in the case of ionising radiation, while the other is probably the RO2 radical formed as a result of photodynamic action. 相似文献
4.
Jerry L. Atwood Hosny Elgamal Gregory H. Robinson Simon G. Bott James A. Weeks William E. Hunter 《Journal of inclusion phenomena and macrocyclic chemistry》1984,2(1-2):367-376
In contrast to aluminum alkyls, alkyl aluminum halides such as EtAlCl2 react with crown ethers to form cation-anion pairs which exhibit the liquid clathrate effect. Specifically, [12-C-4·AlCl2][AlCl3Et] and [18-C-6·AlCl2][AlCl3Et] have been isolated and characterized by X-ray diffraction techniques. The cations show aluminum in an octahedral environment made up of four of the oxygen atoms from the crown and two chlorine atoms. The 12-C-4 derivative crystallizes in the monoclinic space group P21/c with cell constants of a=7.497(4), b=22.121(8), c=12.339(5) Å, =94.99(3)o, and Z=4 for =1.43 g cm–3. Least-squares refinement based on 1413 observed reflections led to a final conventional R value of 0.093. The 18-C-6 complex belongs to the triclinic space group P1 with a=8.414(4), b=12.193(6), c=12.394(6) Å, =73.14(4), =86.07(4), =81.52(4)o, and Z=2 for =1.45 g cm–3. Refinement based on 2605 observed reflections led to R=0.063. The complex aluminum-containing species are related to a class of compounds called aluminoxanes. 相似文献
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BARB FLORIN DAN; IONESCU VLAD; KONING WILLEM DE 《IMA Journal of Mathematical Control and Information》1994,11(4):277-309
In this paper, we deal with the digital output-measurement-feedbackH control problem for Pritchard-Salamon infinite-dimensionalsystems with unbounded input and output operators. A discretePopov-theory-based solution is given in terms of the solvabilityof Kalman-Szegö-Popov-Yakubovitch systems associated withthe equivalent discrete-time time-invariant system obtainedby lifting the T-periodic continuous-time system. 相似文献
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Abstract— Ellipsometric angles and reflectivity of black lipid membranes containing either egg lecithin or chloroplast extracts were measured at a wavelength of 6328 Å. Evidence was found for positive uniaxial anisotropy in membranes of lecithin. If the thickness of those films is assumed to be 62 Å, the refractive index normal to the film surface is 1.471 ± 0.004, and the refractive index parallel to the film surface is 1.454 ± 0.003. The results for membranes of chloroplast extracts also indicate a positive anisotropy in the indices of absorption. 相似文献
10.
Buchmueller KL Hill BT Platz MS Weeks KM 《Journal of the American Chemical Society》2003,125(36):10850-10861
Arylazide mediated photocrosslinking has been widely used to obtain structural constraints in biological systems, even though the reactive species generated upon photolysis in aqueous solution have not been well characterized. We establish a mechanistic framework for formation of adducts between photoactivated 3-hydroxyphenyl azide and RNA. Tethered to an internal site in an RNA duplex via a 2'-amido linkage, photolysis of the aryl azide yields a cross-strand cross-link. Analysis of the ability of reagents with diagnostic reactivities to intercept formation of this cross-strand cross-link supports the assignment that the photoactivated intermediate is the ketenimine or a ketenimine-derived ring expansion product. Neither the initially produced singlet nitrene nor the subsequently formed triplet nitrene contribute to cross-link formation. Argon matrix and time-resolved solution experiments show that photolysis of free 3-hydroxyphenyl azide releases (in 相似文献