Very Unusual (very + unusual)

Distribution by Scientific Domains


Selected Abstracts


Tungsten Oxide and Tungsten Oxide-Titania Thin Films Prepared by Aerosol-Assisted Deposition , Use of Preformed Solid Nanoparticles

EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 10 2007
Uzma Qureshi
Abstract Aerosol-assisted deposition (AAD) was used to deposit films of WO3 from a suspension of solid nanoparticulate WO3 in toluene. Titania films were deposited by the aerosol-assisted chemical vapour deposition of [Ti(OiPr)4] in the presence of WO3 nanoparticles. The WO3 and TiO2 films exhibited photoactivity and photoinduced superhydrophilicity, further the titania films showed very unusual highly crenulated microstructures. These microstructures could not be obtained by sol-gel, atmospheric pressure chemical vapour deposition or evaporation routes. Furthermore, the microstructures could not be obtained from [Ti(OiPr)4] in the absence of nanoparticulate WO3. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source]


ULTRASTRUCTURAL STUDIES ON BIGELOWIELLA NATANS, GEN.

JOURNAL OF PHYCOLOGY, Issue 4 2001
ET SP.
Three isolates from the Provasoli-Guillard National Center for Culture of Marine Phytoplankton at Bigelow Laboratory, previously labeled Pedinomonas sp. and Pedinomonas minutissima from the green algal class Pedinophyceae, have been examined by light microscopy and TEM and shown to belong to the Chlorarachniophyceae, a class of nucleomorph-containing amebae. The three isolates represent the first chlorarachniophycean flagellates to be discovered. The ultrastructure of the cells has been examined in detail, with particular emphasis on the flagellar apparatus, a feature not examined in detail in chlorarachniophytes before. Cells are basically biflagellate, but the second flagellum is represented by a very short basal body only. Flagellar replication has shown this flagellum to be the mature stage, that is, the no. 1 flagellum, whereas the long emergent flagellum is the no. 2 flagellum that shortens into a short basal body during cell division. Mitosis is open with a pair of centrioles at each pole. Emergent flagella are absent during mitosis. Cells may form cysts, and the flagellar basal bodies and part of the flagellar roots are maintained in the cysts. Four microtubular roots emanate from the basal bodies, and the path of one of them is very unusual and very unlike any other known flagellate. No striated roots were observed. Other fine-structural features of the cell include a very unusual type of pyrenoid and a special type of extrusome. Cells are mixotrophic. The three isolates are very similar and are described as Bigelowiella natans, gen. et sp. nov. Ultrastructurally, chlorarachniophytes do not show close relationship to any known group of algae or other protists. [source]


Acrodermatitis chronica atrophicans affecting all four limbs in an 11-year-old girl

BRITISH JOURNAL OF DERMATOLOGY, Issue 2 2002
I. Brzonova
SummaryBorrelia burgdorferi is a major cause of morbidity in wooded area in western Europe and the eastern seaboard of the U.S.A. Diagnosis of late stage infection and associated disorders may be difficult and often requires an array of different diagnostic procedures. Here we report an 11-year-old girl with acrodermatitis chronica atrophicans affecting all four limbs and parts of the trunk. The diagnosis was made on the basis of clinical appearance, serological and histopathological findings, and the lesional detection of B. burgdorferi -specific gene segments by polymerase chain reaction. This very unusual, severe case illustrates that despite being a late manifestation of tick-borne B.burgdorferi infection, usually occurring in adults, acrodermatitis chronica atrophicans may already appear at a young age and may be characterized by extensive skin involvement. [source]


Three-Component Entanglements Consisting of Three Crescent-Shaped Bidentate Ligands Coordinated to an Octahedral Metal Centre

CHEMISTRY - A EUROPEAN JOURNAL, Issue 31 2007
Fabien Durola
Abstract 3,3,-Biisoquinoline ligands (biiq) L, bearing aromatic substituents on their 8 and 8, positions, have been used to generate interwoven systems consisting of three crescent-shaped ligands disposed around an octahedral metal centre. Mono-ligand complexes of the type [ReL(CO)3py]+ (py: pyridine) have also been prepared, leading to sterically non-hindering complexes in spite of the endotopic nature of the chelate used. The three-component entanglements have been prepared by using either FeII or RuII as gathering metal centre. The synthetic procedure is simple and efficient, affording fully characterised complexes as their PF6 or SbCl6 salts. X-ray crystallography clearly shows that the crescent-shaped ligands do not repel each other in the tris-chelate complexes. In an analogous way, the ReI complexes show open structures with no steric repulsion between the L ligand and the ancillary CO or py groups. The FeL3 or RuL3 compounds are very unusual in the sense that, contrary to all the other tris-bidentate chelate complexes made till now, the three organic components are tangled up, in a situation which will be very favourable to the formation of new non trivial topologies of the catenane type. [source]


Head-to-Head Cross-Linked Adduct between the Antitumor Unit Bis(,- N,N,-di- p -tolylformamidinato)dirhodium(II,II) and the DNA Fragment d(GpG)

CHEMISTRY - A EUROPEAN JOURNAL, Issue 25 2006
Helen T. Chifotides Dr.
Abstract Reactions of the compound cis -[Rh2(DTolF)2(CH3CN)6](BF4)2, a formamidinate derivative of the class of antitumor compounds [Rh2(O2CR)4] (R=Me, Et, Pr), with 9-ethylguanine (9-EtGuaH) or the dinucleotide d(GpG) proceed by substitution of the acetonitrile groups, with the guanine bases spanning the RhRh bond, in a bridging fashion, through sites N7/O6. In the case of 9-EtGuaH, both head-to-head (HH) and head-to-tail (HT) isomers are formed, whereas with the tethered bases in d(GpG), only one right-handed conformer HH1R [Rh2(DTolF)2{d(GpG)}] is present in solution. For both cis -[Rh2(DTolF)2(9-EtGuaH)2](BF4)2 and [Rh2(DTolF)2{d(GpG)}], the absence of N7 protonation at low pH and the substantial decrease of the pKa values for N1-H deprotonation, support N7/O6 binding of the bases to the dirhodium core. The N7/O6 binding of the bases is further corroborated by the downfield shift by ,,,4.0 ppm of the 13C NMR resonances for the C6 nuclei as compared to the corresponding resonances of the free ligands. The HH arrangement of the guanine bases in [Rh2(DTolF)2{d(GpG)}] is indicated by the intense H8/H8 ROE cross-peaks in the 2D ROESY NMR spectrum. Complete characterization of the [Rh2(DTolF)2{d(GpG)}] conformer by 2D NMR spectroscopy supports anti- orientation and N (C3,- endo) conformation for both deoxyribose residues. The N-pucker for the 5,-G base is universal in such cross-links, but it is very unusual for platinum and unprecedented for dirhodium HH cross-linked adducts to have both deoxyribose residues in the N-type conformation. The bulk, the nonlabile character, and the electron-donating ability of the formamidinate bridging groups spanning the dirhodium core affect the nature of the preferred dirhodium DNA adducts. Molecular modeling studies performed on [Rh2(DTolF)2{d(GpG)}] corroborate the structural features obtained by NMR spectroscopy. [source]