Results 131 to 140 of about 1,578,947 (161)
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ChemInform Abstract: Model for the Initial Stage in the Oxidative Addition of I2 to Organoplatinum (II) Compounds.

Chemischer Informationsdienst, 1986
AbstractThe 1:1 molar reaction of the iodo‐Pt(II) complex (I) with I2 leads to the stable title complex (II) which is characterized by X‐ray structural analysis (space group P2,2,2" Z=4), UV, and 1H NMR spectral data.
J. A. M. VAN BEEK   +3 more
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ChemInform Abstract: ORGANOPLATINUM(IV) COMPOUNDS PART 1, TRIMETHYLPLATINUM(IV) AZIDE, ME3PTN3

Chemischer Informationsdienst, 1974
AbstractDas aus Kaliumhexachloroplatinat (I) mit Methyllithium (II) hergestellte Trimethyl platinchlorid (III) wird mit Silbersulfat in Aceton in das Sulfat (IV) umgewandelt.
K.‐H. VON DAHLEN, J. LORBERTH
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[Organoplatinum compounds. 1987 update].

Nouvelle revue francaise d'hematologie, 1988
Cisplatin is one of the best available cytotoxic agents particularly in testicular, ovarian and head and neck cancer. However gastrointestinal and renal toxicities preclude greater utilisation. High dose cisplatin (200 mg/m2) has serious neurological side effects.
J M, Extra, M, Espie, F, Calvo, M, Marty
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Photophysical Properties of Organoplatinum(II) Compounds and Derived Self-Assembled Metallacycles and Metallacages: Fluorescence and its Applications

Accounts of Chemical Research, 2016
Over the past couple of decades, coordination-driven self-assembly has evolved as a broad multidisciplinary domain that not only covers the syntheses of aesthetically pleasing supramolecular architectures but also emerges as a method to form new optical materials, chemical sensors, theranostic agents, and compounds with light-harvesting and emissive ...
Manik Lal, Saha   +2 more
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ChemInform Abstract: REACTIONS OF (PI‐1,5‐CYCLOOCTADIENE)ORGANOPLATINUM(II) COMPOUNDS AND THE SYNTHESIS OF PERFLUOROALKYLPLATINUM COMPLEXES

Chemischer Informationsdienst, 1974
AbstractEine Lösung von Kaliumtetrachloroplatinat (I) in Wasser/n‐Propanol setzt sich mit 1,5‐Cyclooctadien (II) zum Platin‐Komplex (III) um, der mit Natriumjodid (IV) ins entsprechende Jodderivat (V) übergeführt werden kann.
H. C. CLARK, L. E. MANZER
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Noncovalent complexes of water‐soluble polymers and organoplatinum compounds as potential time‐release antitumor agents

Makromolekulare Chemie. Macromolecular Symposia, 1988
AbstractThe complexation of appropriate organoplatinum compounds by water‐soluble polymers has the potential to provide a time‐release formulation which might afford a substantial reduction in the severity of side effects associated with use of organoplatinum antitumor agents. Both poly‐(N‐vinylpyrrolidone)(PVP) and poly(N‐vinyl‐5‐methyl‐2‐oxazolidone)(
B. A. Howell   +2 more
openaire   +1 more source

Organoplatinum‐Mediated Synthesis of Cyclic π‐Conjugated Molecules: Towards a New Era of Three‐Dimensional Aromatic Compounds

The Chemical Record, 2014
AbstractThis article describes the most recent developments in the synthesis of three‐dimensional π‐conjugated molecules and the elucidation of their properties made by our research group. Various cycloparaphenylenes (CPPs) of different sizes and a cage‐like 3D molecule were synthesized based on the platinum‐mediated assembly of π‐units and subsequent ...
Shigeru, Yamago   +2 more
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Complexes of Water Soluble Polymers and Organoplatinum Compounds as Potential Time-Release Antitumor Formulations

1988
The serendipitous discovery of the biological activity of cis-dichlorodi-ammineplatinum(II) [“Cisplatin”] by Rosenberg in 1965 spawned an intensive investigation of the chemical and biological properties of this compound and its derivatives (1–6). Cisplatin and derivatives represent a class of very effective, broad spectrum antitumor agents (6).
B. A. Howell   +5 more
openaire   +1 more source

Comparison of metal-hydrogen, -oxygen, -nitrogen and -carbon bond strengths and evaluation of functional group additivity principles for organoruthenium and organoplatinum compounds

Polyhedron, 1988
Abstract The equilibria: LnMX + HY ⇁ LnMY + HX (LnM = (DPPE)MePt or Cp(PMe3)2Ru; X, Y = hydride, alkoxide, hydroxide, amide, alkyl, alkynyl, hydrosulphide, cyanide) have been examined. The equilibrium constants allow for the determination of relative MX, MY bond dissociation energies (BDEs) for each series of compounds.
Henry E. Bryndza   +5 more
openaire   +1 more source

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