and applications

We study an analogue of the classical theory of weights in without assuming that the underlying measure is doubling. Then, we obtain weighted norm inequalities for the (centered) Hardy-Littlewood maximal function and corresponding weighted estimates for nonclassical Calderón-Zygmund operators. We also consider commutators of those Calderón- Zygmund operators with bounded mean oscillation functions (), extending the main result from R. Coifman, R. Rochberg, and G. Weiss, Factorization theorems for Hardy spaces in several variables, Ann. of Math. 103 (1976), 611-635. Finally, we study self-improving properties of Poincaré-B.M.O. type inequalities within this context; more precisely, we show that if is a locally integrable function satisfying for all cubes , then it is possible to deduce a higher integrability result for , assuming a certain simple geometric condition on the functional .     

Synthesis and characterization of [Cu(Me2oxpn)Ni(NO2)(tmen)](ClO4): a single ferrimagnetic dinuclear CuII-NiII complex acting as weak molecule-based magnet

The new heterodinuclear complex [Cu(Me2oxpn)Ni(NO2)(tmen)](ClO4), that exhibits strong antiferromagnetic intramolecular coupling between CuII and NiII ions (ferrimagnetic behavior), shows ferromagnetic ordering at low temperature, due likely to a small canting phenomenon; it is one of the very few compounds made from isolated molecules that lead to cooperative magnetic behavior.     

Direct H atom abstraction from spore photoproduct C-6 initiates DNA repair in the reaction catalyzed by spore photoproduct lyase: evidence for a reversibly generated adenosyl radical intermediate

Spore photoproduct (SP) lyase, which catalyzes the direct reversal of SP (5-thyminyl-5,6-dihydrothymine) to thymine monomers, is the only identified nonphotoactivatable pyrimidine dimer lyase. Unlike DNA photolyase, SP lyase does not contain a flavin cofactor and does not require light for activation. Instead, preliminary studies point to the presence of an iron-sulfur cluster in SP lyase and the requirement for S-adenosylmethionine (AdoMet) for catalytic activity, suggesting that SP lyase belongs to the growing group of iron-sulfur cluster and AdoMet-dependent radical enzymes. Here we provide evidence for the role of AdoMet as a reversible deoxyadenosyl radical generator, which initiates repair by hydrogen atom abstraction from C-6 of SP. Reaction of 6-(3)H-SP, but not methyl-(3)H-SP, with SP lyase and AdoMet results in transfer of (3)H to AdoMet, while no tritiated 5'-deoxyadenosine is observed. When 5'-tritiated AdoMet is used in the reaction with unlabeled SP, transfer of (3)H into the repaired thymine monomers is observed. These results point to the reversible generation of a 5'-deoxyadenosyl radical intermediate, which reacts directly with the DNA lesion to initiate a radical-mediated beta-scission. We also demonstrate that AdoMet is a catalytic cofactor that is not consumed during turnover. Together, these results support a novel radical-based mechanism for the repair of UV-induced DNA damage.     

Automatic determination of inorganic carbon in surface waters

An automated colorimetric procedure was developed for the determination of inorganic carbon in the range 0.3–40.0 mg l^-1, and then modified to handle concentrations in the range 0.01–2.00 mg l^-1. The procedure entailed conversion of carbon dioxide equilibria products to carbon dioxide. By gas dialysis, a portion of this gas was dissolved in a weakly buffered alkaline phenolphthalein solution, and inorganic carbon was determined by measuring the loss in color of the indicator. Calibrations were linear within 1% full scale. When surface water samples were processed by the subject and by alternative methods, the colorimetric carbon results were lower by approximately 1% full scale.     

The mass spectra of some naphthoquinones. Lapachol,isolapachol and related compounds

Several alkylhydroxynaphthoquinones and chemically related cyclic compounds were subjected to mass spectrometric investigation. Fragmentation pathways were elucidated by use of metastable ions, relative intensities of normal ions and accurate mass measurement. In these series, differences in the spectra of 1,2- and 1,4-naphthoquinones are slight. Evidence for ring expansion in ions from furans is suggested.