Results 21 to 30 of about 381,080 (296)

Bis(4-carboxypyridine-2-carboxylato-κ2N,O2)copper(II) dimethyl sulfoxide disolvate

Acta Crystallographica Section E, 2011
In the title complex, [Cu(C7H4NO4)2]·2C2H6OS, the CuII atom is situated on an inversion centre and is N,O-chelated by two monoanionic 4-carboxypyridine-2-carboxylate ligands in a slightly distorted square-planar coordination geometry.
Hossein Aghabozorg, Saba Goodarzi, Masoud Mirzaei, Behrouz Notash   +3 more
doaj   +1 more source

Microbial degradation of dimethylsulphide and related C1-sulphur compounds: organisms and pathways controlling fluxes of sulphur in the biosphere [PDF]

, 2010
Dimethylsulphide (DMS) plays a major role in the global sulphur cycle. It has important implications for atmospheric chemistry, climate regulation, and sulphur transport from the marine to the atmospheric and terrestrial environments.
Boden, Rich, Myronova, Natalia, Schäfer, Hendrik   +2 more
core   +1 more source

9-(5-Bromo-1H-indol-3-yl)-1,2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione dimethyl sulfoxide monosolvate

Acta Crystallographica Section E, 2012
In the title compound, C21H19BrN2O2·C2H6OS, the indole ring system is essentially planar, with a maximum deviation of 0.050 (3) Å for the non-bridgehead C atom adjacent to the N atom.
Ahmed El-Khouly, Sema Öztürk Yildirim, Ray J. Butcher, Rahime Şimsek, Cihat Şafak   +4 more
doaj   +1 more source

Synthesis and (spectro)electrochemistry of mixedvalent diferrocenyl–dihydrothiopyran derivatives [PDF]

, 2015
Three novel diferrocenyl complexes were prepared and characterised. 2,2-Diferrocenyl-4,5-dimethyl- 3,6-dihydro-2H-thiopyran (1, sulphide) was accessible by the hetero-Diels–Alder reaction of diferrocenyl thioketone with 2,3-dimethyl-1,3-butadiene ...
Aguirre-Etcheverry, Alexander Hildebrandt, Allen, Barlow, Barrière, Barrière, Becke, Bruno Therrien, Ceccon, Costuas, D'Alessandro, Delgado-Pena, Denifl, Diallo, Diallo, Dominique Miesel, Dong, Dong, Drabowicz, Duggan, Enders, Farrugia, Ferguson, Filipczyk, Fourie, Geiger, Geiger, Gericke, Glover, Gray, Gritzner, Grzegorz Mlostoń, Heinrich Lang, Hildebrandt, Hildebrandt, Hildebrandt, Hildebrandt, Hildebrandt, Hush, Inamoto, Jones, Kaleta, Kaleta, Kienz, Konrad Kowalski, Kotz, Kowalski, Kowalski, Krejcik, Lapinte, Larsen, Lee, Lehrich, Linseis, Lohan, Lohan, Miesel, Mücke, Nafady, Nemykin, Nemykin, O'Connor Salazar, Paul, Petrov, Petrov, Pfaff, Pfaff, Pfaff, Pfaff, Pichlmaier, Poppitz, Rafał Czerwieniec, Rafał Karpowicz, Ratner, Ribou, Robin, Rulkens, Sheldrick, Snyder, Speck, Speck, Swarts, Ward, Weeb, Winter, Xie, Xie, Yamaguchi   +87 more
core   +3 more sources

(2-{[4-(Chloridomercuryl)phenyl]iminomethyl}pyridine-κ2N,N′)diiodidomercury(II) dimethyl sulfoxide monosolvate

Acta Crystallographica Section E, 2013
The title dimethyl sulfoxide solvate, [Hg2(C12H9ClN2)I2]·C2H6OS, features tetrahedrally and linearly coordinated HgII atoms. The distorted tetrahedral coordination sphere is defined by chelating N atoms that define an acute angle [69.6 (3 ...
Edward R. T. Tiekink, Seik Weng Ng, Imliwati Longkumer, Tushar S. Basu Baul   +3 more
doaj   +1 more source

JNK inhibition sensitises hepatocellular carcinoma cells but not normal hepatocytes to the TNF-related apoptosis-inducing ligand. [PDF]

, 2009
Background: cJun terminal kinase (JNK) is constitutively activated in most hepatocellular carcinomas (HCCs), yet its exact role in carcinogenesis remains controversial.
Bruns, Christiane, Camaj, Peter, De Toni, Enrico, Eichhorst, Sören T., Gallmeier, Eike, Gerbes, Alexander L., Göke, Burkhard, Kolligs, Frank T., Mucha, Simon R., Rizzani, Antonia, Thasler, Wolfgang E.   +10 more
core   +1 more source

2-(5-Bromo-1H-indol-3-yl)-4-(4-bromophenyl)-5-(4-chlorobenzoyl)-1H-pyrrole-3-carbonitrile dimethyl sulfoxide monosolvate

IUCrData, 2016
In the title solvated compound, C26H14Br2ClN3O·C2H6OS, the indole ring is inclined to the central pyrrole ring by 25.7 (2)°. The chlorobenzene ring and the bromobenzene rings subtend dihedral angles of 56.5 (2) and 53.4 (2)°, respectively, with the ...
Y. AaminaNaaz, Jayabal Kamalraja, G. Vimala, Paramasivam T. Perumal, A. SubbiahPandi   +4 more
doaj   +1 more source

3-[1-(3-Hydroxybenzyl)-1H-benzimidazol-2-yl]phenol dimethyl sulfoxide monosolvate

Acta Crystallographica Section E, 2012
Crystals of the title compound were obtained as a 1:1 dimethyl sulfoxide solvate, C20H16N2O2·C2H6O. The molecular conformation of the organic molecule is similar to that in the previously reported unsolvated structure [Eltayeb et al.
Magdalena Quezada-Miriel, Alcives Avila-Sorrosa, Juan Manuel German-Acacio, Reyna Reyes-Martínez, David Morales-Morales   +4 more
doaj   +1 more source

Spectroscopic Properties of Polycyclic Aromatic Compounds. Examination of Nitromethane as a Selective Fluorescence Quenching Agent for Alternant Polycyclic Aromatic Nitrogen Hetero-Atom Derivatives [PDF]

, 1992
Article on the spectroscopic properties of polycyclic aromatic compounds and an examination of nitromethane as a selective fluorescence quenching agent for alternant polycyclic aromatic nitrogen hetero-atom ...
Acree, William, Kimihiro, Hiruta, Langhals, Heinz, Tanga, Mary, Tokita, Sumio, Tucker, Sheryl A.   +5 more
core   +1 more source

Lithium solvation in dimethyl sulfoxide-acetonitrile mixtures [PDF]

, 2014
We present molecular dynamics simulation results pertaining to the solvation of Li+ in dimethyl sulfoxide-acetonitrile binary mixtures. The results are potentially relevant in the design of Li-air batteries that rely on aprotic mixtures as solvent media.
Calvo, Ernesto Julio, Laria, Daniel Hector, Semino, Rocio, Zaldivar, Gervasio   +3 more
core   +1 more source