The title compound, C(18)H(15)OP·C(13)H(17)N(2)O(3), belongs to a series of mol-ecular systems based on triphenyl-phosphine oxide. The O atom of the oxide group acts as an acceptor for hydrogen bonds from -OH groups of the nitronyl nitroxide. The crystal structure is stabilized by O-H⋯O hydrogen bonds.

In the title compound, [Ni(NO(3))(2)(C(24)H(20)N(2))(2)], the Ni(II) atom has a distorted pseudo-octa-hedral coordination geometry defined by two chelating nitrate groups and two pyridine N atoms of the monodentate N-(triphenyl-meth-yl)pyridin-2-amine ligands. Intra-molecular N-H⋯O hydrogen bonds help to establish the configuration.

Dielectric relaxation measurements on supercooled triphenyl phosphite show that time-temperature superposition (TTS) is obeyed for the primary relaxation process at low temperatures. Measurements on other molecular liquids close to the calorimetric glass transition indicate that TTS is linked to an omega(-1/2) high-frequency decay of the loss, while the loss peak width is nonuniversal.

Soluble polymer-supported chemistry is a technology that allows the blending of the benefits of polymer-supported synthesis and solution-phase chemistry. Herein, we describe our recent efforts in this area targeted at exploring the scope of poly(ethylene glycol) (PEG) as the matrix. Specifically we describe the use of PEG as a support for triphenyl phosphine and for the Stille reaction.

Nimesulide, a COX-2 selective drug, possesses anti-inflammatory and analgesic properties. Moreover, it has low gastrointestinal and renal toxicity. This paper presents industrially viable, new and improved synthesis of nimesulide starting from o-chloro nitrobenzene. The reaction with triphenyl phosphate yields 2-phenoxy nitrobenzene (90%) followed by reduction and mesylation and finally selecti...

The crystal structure of the title compound, [Ru(C(12)H(12)O(6))(C(18)H(15)P)(2)(CO)], confirms its formulation as a ruthenabenzofuran, with a slightly distorted octa-hedral coordination environment at the Ru(II) ion, and mutually trans triphenyl-phosphine ligands. The metallabicyclic ring system is essentially planar (maximum deviation 0.059 Å).

Benzylic C-H lithiation of 3,4-benzothiophane and subsequent treatment with triphenyl- or trimethylchlorosilane under a variety of conditions leads to α,α- rather than α,α'-bis-silylation products as a consequence of anion stabilization by R3Si and very fast deprotonation of the intermediate monosilylated product, even with a sterically bulky base such as lithium diisopropylamide.

In previous work, Vibrio proteolyticus 5S rRNA was shown to stabilize 13-50 nucleotide "guest" RNA sequences for expression in Escherichia coli. The expressed chimeric RNAs accumulated to high levels in E. coli without being incorporated into ribosomes and without obvious effects on the host cells. In this work, we inserted sequences encoding known aptamers recognizing a protein and an organic ...

the wittig reaction rate can be dramatically enhanced by irradiation of the reaction mixture containing an aldehyde or ketone; methoxymethyl(triphenyl)phosphonium chloride, potassium t-butoxide, and t buoh with a commercial microwave oven. carbonyl compound are converted to witting products within three min. in good yields.