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排序方式: 共有245条查询结果,搜索用时 15 毫秒
1.
Phelps T. J. Siegrist R. L. Korte N. E. Pickering D. A. Strong-Gunderson J. M. Palumbo A. V. Walker J. F. Morrissey C. M. Mackowski R. 《Applied biochemistry and biotechnology》1994,45(1):835-845
Applied Biochemistry and Biotechnology - Soil column studies were used to evaluate petroleum hydrocarbon (PHC) remediation in soils from Kwajalein Atoll. Treatments included controls, and... 相似文献
2.
Palumbo A. V. Scarborough S. P. Pfiffner S. M. Phelps T. J. 《Applied biochemistry and biotechnology》1995,51(1):635-647
Applied Biochemistry and Biotechnology - The US Department of Energy, Office of Technology Development, has supported a field-scalein situ demonstration of trichloroethylene (TCE) bioremediation at... 相似文献
3.
Mild treatment of sepiomelanin and biosynthetic eumelanins with NaBH4 in 0.1 N NaOH leads to the isolation of 5,6-dihydroxyindole-2-carboxylic acid (), a component of structural interest which may account for most of the degradation products of melanins so far obtained. 相似文献
4.
5.
Palumbo Anthony V. Lee S. Y. Boerman Patrice 《Applied biochemistry and biotechnology》1994,45(1):811-822
Applied Biochemistry and Biotechnology - EDTA degradation by anAgrobacterium sp. has been examined by quantifying14C-labeled CO2 produced from iron-[2-14C] EDTA and by measured loss of nonlabeled... 相似文献
6.
Burlage Robert S. Palumbo Anthony V. Heitzer Armin Sayler Gary 《Applied biochemistry and biotechnology》1994,45(1):731-740
Applied Biochemistry and Biotechnology - Reporter strains of bacteria were tested using soil samples from several sites near a leaking fuel oil storage facility. The reporter bacteria utilized the... 相似文献
7.
Ohne Zusammenfassung 相似文献
8.
M. Palumbo F. Baccichetti C. Antonello O. Gia A. Capozzi S. Marciani Magno 《Photochemistry and photobiology》1990,52(3):533-540
The furocoumarin derivative 3,4'-dimethyl-8-methoxypsoralen (DMe-8-MOP) exhibits remarkable antiproliferative activity, but is devoid of skin phototoxicity. To gain insight into this peculiar behaviour we investigated non-covalent and covalent binding of DMe-8-MOP to calf thymus DNA, along with DNA-synthesis inhibition and mutagenic activity. The non-covalent interaction of DMe-8-MOP with the nucleic acid is quite poor as shown by equilibrium dialysis, spectroscopic, chiroptical and hydrodynamic techniques. However, it exhibits relevant photobinding ability to DNA using both isolated nucleic acid samples and cellular systems. Unlike the large majority of congeners, DMe-8-MOP undergoes predominantly photochemical monoaddition to the double helical polynucleotide. Upon examination of the products obtained by enzymatic hydrolysis of DMe-8-MOP photomodified DNA, the formation of an unusual furan side adduct is proposed, which could account for the peculiar photochemical and photobiological properties of the 3,4'-dimethyl furocoumarin derivative. 相似文献
9.
Dieuwertje K. Modder Chad T. Palumbo Iskander Douair Rosario Scopelliti Laurent Maron Marinella Mazzanti 《Chemical science》2021,12(17):6153
The redox chemistry of uranium is dominated by single electron transfer reactions while single metal four-electron transfers remain unknown in f-element chemistry. Here we show that the oxo bridged diuranium(iii) complex [K(2.2.2-cryptand)]2[{((Me3Si)2N)3U}2(μ-O)], 1, effects the two-electron reduction of diphenylacetylene and the four-electron reduction of azobenzene through a masked U(ii) intermediate affording a stable metallacyclopropene complex of uranium(iv), [K(2.2.2-cryptand)][U(η2-C2Ph2){N(SiMe3)2}3], 3, and a bis(imido)uranium(vi) complex [K(2.2.2-cryptand)][U(NPh)2{N(SiMe3)2}3], 4, respectively. The same reactivity is observed for the previously reported U(ii) complex [K(2.2.2-cryptand)][U{N(SiMe3)2}3], 2. Computational studies indicate that the four-electron reduction of azobenzene occurs at a single U(ii) centre via two consecutive two-electron transfers and involves the formation of a U(iv) hydrazide intermediate. The isolation of the cis-hydrazide intermediate [K(2.2.2-cryptand)][U(N2Ph2){N(SiMe3)2}3], 5, corroborated the mechanism proposed for the formation of the U(vi) bis(imido) complex. The reduction of azobenzene by U(ii) provided the first example of a “clear-cut” single metal four-electron transfer in f-element chemistry.Both a masked and the actual complex [U(ii){N(SiMe3)2}3]+ effect the reduction of azobenzene to yield a U(vi) bis-imido species providing the first example of a “clear-cut” metal centred four-electron reduction in f-element chemistry. 相似文献
10.
Buscemi S Pace A Palumbo Piccionello A Macaluso G Vivona N Spinelli D Giorgi G 《The Journal of organic chemistry》2005,70(8):3288-3291
The reaction of 3-benzoyl-5-perfluoroalkyl-1,2,4-oxadiazoles with hydrazine has been investigated, evidencing the possibility of competitive reaction paths. Nucleophilic addition of the hydrazine to the electrophilic C(5) of the 1,2,4-oxadiazole ring, followed by ring opening and ring closure with enlargement, leads with high yield and in very mild experimental conditions to the formation of Z-oximes of 3-perfluoroalkyl-6-phenyl-2H-1,2,4-triazin-5-ones (11a-c) as major products of the reaction. In turn, the hydrazine can attack the electrophilic carbonyl carbon giving 4-perfluoroacylamino-5-phenyl-2H-1,2,3-triazoles (13a-c) through the well-known Boulton-Katritzky rearrangement of the intermediate hydrazones. 相似文献