Photophysical properties of novel fluorescent poly(oxyethylene phosphate) tris(β-diketonate) europium (III) complexes

In the present study, photophysical properties of fluorescent poly(oxyethylene phosphate) tris(β-diketonate) europium (III) complexes have been studied by means of stationary and time-resolved fluorescence spectroscopy (in ethanol at room temperature). The luminescent quantum yields and efficiency for the energy transfer from β-diketonate ligands to Eu(III) ion have been determined for the studied complexes by using diffusion-enhanced fluorescence resonance energy transfer. Obtained results show effect of the polymer ligands upon photophysical properties of the complexes and a relation has been established with length of the oxyethylene spacer between two phosphonate groups. The Förster radiuses of the synthesized compounds with SulfoRhodamine 101 as acceptor have been calculated. Measured distances between molecules of the donors and acceptor at identical acceptor/donor molar ratios have been illustrated the difference in structure of the ternary and polymer complexes in solution even at low concentration.     

Thermal analysis of cobalt,nickel and copper complexes of 2-aminothiazole

The thermal decomposition of 2-aminothiazole (2-amt) complexes of general formula M(2-amt)₂X₂ [M = Co(II) and Cu(II)] and Ni(2-amt)₄X₂ [X = Cl and Br] have been studied in air and argon by TG and DTG as well as by DTA in nitrogen; end products from the decompositions in air have been characterised by X-ray powder diffraction. Decomposition stoichiometries have been proposed and factors governing the thermal decomposition have been discussed.     

Palladium‐Catalyzed Direct CH Functionalization of Benzoquinone

A direct Pd‐catalyzed C? H functionalization of benzoquinone (BQ) can be controlled to give either mono‐ or disubstituted BQ, including the installation of two different groups in a one‐pot procedure. BQ can now be directly functionalized with aryl, heteroaryl, cycloalkyl, and cycloalkene groups and, moreover, the reaction is conducted in environmentally benign water or acetone as solvents.     

Oxidative Conversion of a Europium(II)‐Based T1 Agent into a Europium(III)‐Based paraCEST Agent that can be Detected In Vivo by Magnetic Resonance Imaging

The Eu^II complex of 1,4,7,10‐tetraazacyclododecane‐1,4,7,10‐tetraacetic acid (DOTA) tetra(glycinate) has a higher reduction potential than most Eu^II chelates reported to date. The reduced Eu^II form acts as an efficient water proton T₁ relaxation reagent, while the Eu^III form acts as a water‐based chemical exchange saturation transfer (CEST) agent. The complex has extremely fast water exchange rate. Oxidation to the corresponding Eu^III complex yields a well‐defined signal from the paraCEST agent. The time course of oxidation was studied in vitro and in vivo by T₁‐weighted and CEST imaging.     

Constructing orthogonal pandiagonal Latin squares and panmagic squares from modular n‐queens solutions

In this article, we show how to construct pairs of orthogonal pandiagonal Latin squares and panmagic squares from certain types of modular n‐queens solutions. We prove that when these modular n‐queens solutions are symmetric, the panmagic squares thus constructed will be associative, where for an n × n associative magic square A = (a_ij), for all i and j it holds that a_ij + an?i?1,n?j?1 = c for a fixed c. We further show how to construct orthogonal Latin squares whose modular difference diagonals are Latin from any modular n‐queens solution. As well, we analyze constructing orthogonal pandiagonal Latin squares from particular classes of non‐linear modular n‐queens solutions. These pandiagonal Latin squares are not row cyclic, giving a partial solution to a problem of Hedayat. © 2007 Wiley Periodicals, Inc. J Combin Designs 15: 221–234, 2007     

Chiral and water‐soluble poly(2‐oxazoline)s

We describe the synthesis and characterization of the first water‐soluble and chiral poly(2,4‐disubstituted‐2‐oxazoline)s. While poly(2,4‐dimethyl‐2‐oxazoline)s are water soluble up to 100 °C, aqueous solutions of poly(2‐ethyl‐4‐methly‐2‐oxazoline) exhibit a lower critical solution temperature. This is discussed in context with its constitutional isomers poly(2‐oxazoline)s and poly(2‐oxazine)s. Circular dichroism spectroscopy revealed strong Cotton effects, which are also responsive to temperature in aqueous solution. It is therefore hypothesized that structures, comparable to polyproline helices, are formed in aqueous solution. In contrast to polyproline, poly(2,4‐disubstituted‐2‐oxazoline)s are highly water soluble and therefore represent very interesting pseudo‐polypeptides that may be useful to develop responsive biomimetic biomaterials. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

Gas collection efficiency of annular denuders: A spreadsheet-based calculator

Denuders are widely used for atmospheric analysis. Annular denuders are especially well-suited for preconcentration of trace gases compared to simpler single tube designs. While traditionally coated annular denuders have both bounding surfaces that behave as sinks, annular denuders/membrane-based scrubbers with the same basic geometric design and with only one of the annular surfaces functioning as sink (e.g., a membrane tube whose outer surface behaves as a sink disposed within an inert jacket tube) have become common. However, the gas collection efficiency of such devices cannot be expressed as a simple equation with fixed constants and there is no presently available tool to a priori determine the denuder performance or to design denuders with specific removal efficiencies at specific sampling rates. This paper presents a simple to use “spreadsheet calculator” for concentric annular denuders of any dimension based on known solutions to analogous heat transfer problems. The results from the present spreadsheet calculator are compared with results from a commercial computational fluid dynamics package (Fluent™; this takes significant expertise and development effort to run)—the two approaches produce essentially the same results. The present spreadsheet calculator can be used easily and simply without training and will be a useful tool for denuder users and designers.     

On the tautomerism of 1-phenyl-3-substituted-pyrazol-5-ones and their photoinduced products — experimental and theoretical UV spectral analysis

A detailed experimental and theoretical UV-spectral analysis of the tautomeric forms of 3-methyl-1-phenyl pyrazol-5-one and 1,3-diphenyl pyrazol-5-one as well as of the UV-irradiated photoinduced products of the latter compound were carried out. The experimental UV-spectra were compared with the theoretical ones obtained by CIS/6-31G**. Selected geometrical parameters of the different tautomers were estimated by ab initio calculations using the RHF/6-31G** level of theory and basis set, which have also been discussed with a view to the corresponding UV-results.