[(Ph3P)3Ru(L)(H)2] (where L = H2 (1) in the presence of styrene, Ph3P (3), and N2 (4)) cleave the Ph-X bond (X = Cl, Br, I) at RT to give [(Ph3P)3RuH(X)] (2) and PhH. A combined experimental and DFT study points to [(Ph3P)3Ru(H)2] as the reactive species generated upon spontaneous loss of L from 3 and 4. The reaction of 3 with excess PhI displays striking kinetics which initially appears zeroth...

a new hybrid nanomaterial was developed by immobilization of phosphomolybdate anions on the surface of modified magnetite nanoparticles with quaternary phosphonium cations. silica coated magnetic nanoparticles supported phosphonium cations, ph3p+-scmnps, were prepared by covalent attachment of chloropropylsilyl groups on the surface of silica coated magnetite nanoparticles and next reaction wit...

Di(4-nitrobenzoyloxy)iodo]benzene (1), a hypervalent iodine compound, is easy to prepare and stable as solid, was shown be useful functional group transforming agent in this report. Oxidative synthesis of symmetrical disulfides from thiols the presence compound 1 alone performed 58–100% yields. Furthermore, ESI-MS demonstrated that premixing Ph3P yields corresponding acyloxyphosphonium, which c...

Research on the one-electron reduced analogue of NO, namely nitroxyl (HNO/NO(-)), has revealed distinguishing properties regarding its utility as a therapeutic. However, the fleeting nature of HNO requires the design of donor molecules. Metal nitrosyl (MNO) complexes could serve as potential HNO donors. The synthesis, spectroscopic/structural characterization, and HNO donor properties of a {CoN...

Z. Naturforsch. 51 b, 801-805 (1996); received December 4, 1995 Carbodiimide, Gold Complexes, (Phosphine)gold Carbodiimides The reaction of N,N'-bis(trimethylsilyl)carbodiimide with equimolar quantities of tris[(triphenylphosphine)gold]oxonium tetrafluoroborate in dichloromethane at -40°C gives high yields of a trinuclear complex {[(Ph3P)Au]2NCN[Au(PPh3)]}+ BF4~(1). According to variable temper...

This so-called Wittig reaction has a number of advantages over other olefination methods; in particular, it occurs with total positional selectivity (that is, an alkene always directly replaces a carbonyl group). By comparison, a number of other carbonyl olefination reactions often occur with double-bond rearrangement. In addition, the factors that influence Eand Z-stereoselectivity are well un...

The reactivity of phosphenium dication [(Ph3P)2C-P-NiPr2](2+), 1(2+), towards pyridine N-oxide (O-py) has been investigated. The resulting oxophosphonium dication [(Ph3P)2C(NiPr2)P(O)(O-py)](2+), 2(2+), was surprisingly stabilized by a less nucleophilic O-py ligand instead of pyridine (py). This compound was then identified as an analogue of the elusive Criegee intermediate as it underwent oxyg...

Tris(triphenylphosphine)gold(I) chloride was found to form a crystalline phase with two molecules of dichloromethane. In the crystal the chlorine atom is almost fully dissociated from the [(Ph3P)3Au] cation. The gold atom shows only a minor displacement from the plane of the phosphorus atoms (sum of the angles P-Au-P 355.35!; d(Au-Cl) 2.7962(6) Å), very similar to the geometry of the solvent-fr...

Reactions of (1) [Q]2[Fe4S4(SC(CH3)3)4] and the fluorous thiols HS(CH2)nRf8 (n = 2, 3; Rf8 = (CF2)7CF3)), or (2) [Na]2[Fe4S4(S(CH2)nRf8)4] (n = 2, 3) and [PhCH2P((CH2)3Rf6)3][Br] or [PPN][Cl] (PPN = Ph3P[horiz bar, triple dot above]N[horiz bar, triple dot above]PPh3), give the title compounds [Q]2[Fe4S4(S(CH2)nRf8)4], comprised of a fluorous dianion and in some cases fluorous cations, with (1) ...

Good quality colloidal nanocrystals of metastable orthorhombic phase of AgInS2 obtained by decomposing the single-precursor [(Ph3P)2AgIn(SCOPh)4] in a mixture of dodecanethiol and oleic acid at 125-200 degrees C, exhibit significant third order non-linear optical properties.