Search results for "phosphine"
showing 10 items of 618 documents
Anti-tumor activity of two binuclear gold(I) complexes with bridging dithiolate ligands
1986
Abstract Two new binuclear complexes of gold with bridging dithiolate ligands were synthesized and characterized: (o3PAu)2(μ-DTE) and (Et3PAu)2(μ-DMTA); H2DTE=dithioerylthritol and H2DMTA=2,5-dimer- capto-1-thia-3,4-diazole. These compounds and three gold compounds with antiarthritic activity (gold sodium thiomalate, gold thioglucose and Et3PAuCl) were tested for antitumor activity using the Ehrlich- Ascites tumor cell in mice. Only (o3PAu)e(μ-DTE) showed significant activity.
In situ generation of Ph3PO in cyanido-bridged heterometallic {FeIIILnIII}2 molecular squares (Ln = Eu, Sm)
2019
Two new examples of cyanido-bridged {FeIIILnIII}2 molecular squares, with pyim and PPh3O as capping ligands at the LnIII sites, exhibit weak antiferromagnetic interactions [Ln = Eu (1), Sm (2), pyim = 2-(1H-imidazol-2-yl)pyridine, PPh3PO = triphenylphosphine oxide].
Phosphororganische Verbindungen, 64: Allyl‐Propenyl‐Umlagerungen Das elektrochemische Verhalten einiger Propenylverbindungen
1970
Allyl-aryl-sulfone, Allyl-diphenyl-phosphinoxid, Allylphosphonsaure-diathylester, Allyl-triphenyl-phosphoniumbromid und Allyl-triphenyl-arsoniumbromid lagern sich an basischem Al2O3 in die entsprechenden 1-Propenyl-Verbindungen um. Allyl-diphenyl-phosphin und Diallyl-phenyl-phosphin isomerisieren sich unter Mitwirkung von Natriumathylat zu den entsprechenden 1-Propenyl-Verbindungen. Die Allyl- und 1-Propenyl-Verbindungen werden IR- und NMR-spektroskopisch sowie polarographisch charakterisiert. — Bei der kathodischen Spaltung von 1-Propenyltriphenyl-phosphoniumbromid entstehen 92% Triphenylphosphin und Propen. 1-Propenyl-phenyl-sulfon wird elektrochemisch in Propen und Benzol-sulfinsaure auf…
Stereospezifische Überführung chiraler acyclischer tertiärer Phosphinsulfide in die entsprechenden tertiären Phosphinoxide mit Dimethylsulfoxid (DMSO)
1975
Die Uberfuhrung chiraler acyclischer tertiarer Phosphinsulfide in die entsprechenden tertiaren Phosphinoxide mit DMSO in saurer Losung erfolgt unter vollstandiger Inversion der Konfiguration am zentralen Phosphoratom. Aufgrund dieses stereochemischen Verlaufs wird ein Mechanismus fur die Reaktion zur Diskussion gestellt. Stereospecific Conversion of Chiral Acyclic Tertiary Phosphine Sulfides into the Corresponding Tertiary Phosphine Oxides by Means of Dimethyl Sulfoxide (DMSO) The conversion of chiral acyclic tertiary phosphine sulfides into the corresponding tertiary phosphine oxides by means of DMSO in acidic solution proceeds with complete inversion of configuration at the central phosph…
The dimerization of substituted 3-TMSO-1-alkynes with (φ3P)3RhCl
1987
Abstract 3-Trimethylsilyloxy-1-alkynes were prepared from 3-hyroxy-1-alkynes and dimerized with (φ3P)3RhCl as a catalyst. The influence of a steric effect on the rates of dimerization is demonstrated.
Acid-Promoted Rearrangement of the Metalated Thienyl Rings in Dirhodium(II) Complexes with Thienyl Phosphines as Ligands
2006
Several mono- and bis-cyclometalated compounds have been prepared and characterized from the thermal reaction of dirhodium(II) tetraacetate and tris(2-thienyl)phosphine, P(2-C4H3S)3 (1), in toluene/acetic acid mixtures. In refluxing acetic acid, the mono-cyclometalated compound Rh2(O2CCH3)3[(2-C4H2S)P(2-C4H3S)2] (CH3CO2H)2 (2A) isomerizes to Rh2(O2CCH3)3[(3-C4H2S)P(2-C4H3S)2](CH3CO2H)2 (2B), which results from the selective rearrangement of the metalated ring from a 2-thienyl to a 3-thienyl structure. In the same conditions, the bis-cyclometalated compounds of formula Rh2(O2CCH3)2[(2-C4H2S)P(2-C4H3S)2]2(CH3CO2H)2 and with head-to-tail (3AA) or head-to-head (4AA) configuration of the phosphi…
Phosphororganische Verbindungen, 65. Die selektive Abspaltung von Allylgruppen aus Allylphosphonium‐, ‐arsonium‐ und ‐sulfoniumsalzen und aus Allylsu…
1970
KCN spaltet Allylphosphonium-, -arsonium- und -sulfoniumsalze in Methacrylnitril und tertiare Phosphine, tertiare Arsine und Thioather auf. Durch alternierende Cyanolyse und Quartarisierung konnen Phosphonium- und Arsoniumsalze mit vier verschiedenen Liganden aufgebaut werden. Allylammoniumsalze, Allylphosphinoxide und -phosphonsaureester konnen nicht gespalten werden. Dagegen liefern Allylsulfone mit KCN in guten Ausbeuten Methacrylnitril und Sulfinsauren. Organic Phosphorus Compounds, 65. The Selective Elimination of Allyl Groups from Allylphosphonium, -arsonium and -sulfonium Salts and from Allyl sulfones by Cyanolysis KCN cleaves allylphosphonium, -arsonium, and -sulfonium salts to give…
Orthometallation reaction in dirhodium(II) compounds. Selective formation of doubly-metallated compounds with head-to-head structure
1993
Abstract The reaction of the mono-metallated compound Rh 2 (O 2 CCH 3 ) 3 [(C 6 H 4 )P(CH 3 ) (C 6 H 5 )]·2(HO 2 CCH 3 ) with PPh 3 (1:1 molar ratio) has been studied by 31 P NMR spectroscopy. The reaction yields the doubly-metallated compound Rh 2 (O 2 CCH 3 ) 2 [(C 6 H 4 ) P(CH 3 )(C 6 H 5 )]p(C 6 H 4 )P(C 6 H 5 ) 2 ]·2(HO 2 CCH 3 ) with a head-to-head (H-H) configuration. An intermediate reaction compound, not previously observed, has been spectroscopically detected in solution. Analogous intermediate compounds have been detected using P( p -CH 3 C 6 H 4 ) 3 and P( p -ClC 6 H 4 ) 3 instead of triphenylphosphine.
Dinuclear Rh(II) complexes in styrene hydroformylation. Enhancement of catalytic activity through orthometalation
1995
Three dirhodium(II) compounds including orthometalated PPh3 ligands have been tested as catalytic precursors for the hydroformylation of styrene. The activities obtained and the wide range of selectivities have been compared to the same reaction performed with RhH(CO)(PPh3)3, Rh2(O2CCH3)4 and various amounts of triphenylphosphine.
ortho-Metalated Dirhodium(II) Catalysts Immobilized on a Polymeric Cross-Linked Support by Copolymerization. Study of their Catalytic Activity in the…
2008
Chiral ortho-metalated dirhodium(II) compounds containing the phosphine P(p-CH2═CHC6H4)3 have been efficiently immobilized by radical copolymerization with styrene and 1,4-divinylbenzene. Their cat...