Platinum Metals Rev., 1979, 23, (4), 157
ABSTRACTS: October 1979
Abstracts: of current literature on the platinum metals and their alloys
Magnetic Properties of Supported Platinum-Iron Alloys
c. h. bartholomew, j. h. anderson and m. boudart, J. Chem. Soc., Faraday Trans. I, 1979, 75, (2), 257–261
The magnetic susceptibility χ of small particles of Pt–Fe alloys was measured on 9.4 wt.% Pt−Fe (90/10)/C (where 9.4 wt.% is a mixture of 9.4% metal alloy and 90.6 wt.% C and (90/10) refers to the respective molar % of Pt and Fe in the alloy) and 12.1 wt.% Pt−Fe (50/50)/C, at 77−700K in H2 and O2. High temperature values of χ correspond to the paramagnetic behaviour of bulk alloys, whereas low temperature values indicate superparamagnetism. At room temperature, H2 removes only part of O2 preadsorbed at the surface of these alloys.
Clusters and Surfaces
e. l. muetterties, t. n. rhodin, e. band, c. f. bruckzer and w. r. pretzer, Chem. Rev., 1979, 79, (2), 91–137
A review of cluster and surface chemistry is presented. The metal cluster family, including all platinum group metal clusters and their crystallographic structures, and molecular clusters with their structural details for halide, carbonyl, binary isocyanide, sulphur and other molecules are examined. Structural comparisons between the chemisorbed state and metal clusters by various adsorption studies are stated, and thermochemical quantities are discussed. (295 Refs.)
Low-Temperature Specific Heat of Glassy and Crystallised Pd0·775Cu0·06Si0·165 Alloys
j. c. lasjaunias, a. ravex and d. thoulouze, J. Phys. F: Metal Phys., 1979, 9, (5), 803–814
The specific heats of Pd0.775Cu0.06Si0.165 alloys were measured between 30 mK and 1-2K successively in glassy and polycrystalline phases obtained by annealing at 400−550°C. Specific heat was dominated by a hyperfine T−2 term at below 80 mK, almost independent of the structure. The short-range order remained almost unchanged from the crystalline to the glassy states.
The Wear Resistance of a Liquid Quenched Metallic Glass
p. g. boswell, J. Mater. Sci., 1979, 14, (6), 1505–1507
The relative wear resistances of amorphous and partially crystalline specimens of a liquid-quenched Pd781Cu55Si164 alloy were measured. Plots were drawn of the average wear rates for the two alloys, and also of the Vickers hardness ratios as a function of the maximum temperature of the amorphous alloy. Wear rate and hardness decreased slightly between 640−690K, then increased dramatically at ∼700K, then dropped away as rapidly. This behaviour implies that the wear resistance of the partially crystalline alloy is mostly controlled by crack nucleation and growth and not by specimen hardness.
Photoemission (XPS, UPS) Studies of Pd-Si Metallic Glasses
p. oelhafen, m. liard, h.-j. guntherodt, k. berresheim and h. d. polaschegg, Solid State Commun., 1979, 30, (10), 641–644
The valence bands of glassy Pd100−xSix (15 ≤ x ≤21) and pure Pd were studied by XPS and UPS. The band spectra of the alloys show a strongly reduced density of states at the Fermi energy, EF, compared to Pd. The electron states near EF for the glassy alloys have mainly d-character. This agrees with recent measurements of low temperature specific heat, the magnetic susceptibility and the optical reflectivity.
On the Extremely High Thermodynamic Stability of Pd-Th Alloys
h.–j. schaller, Z. Naturf. A, 1979, 34, (4), 465–468
The thermodynamic properties of Pd-Th solid solutions containing 0−16 at.% Th were determined at 700−800°C with CaF2 solid electrolyte cells. The mixing behaviour of the alloys is characterised by extreme negative deviations from ideality, up to −410kJ/mol for the partial molar excess free energy of Th. The great stability is attributed to electronic interactions brought about by the transfer of the Th valence electrons to the electron gas of the alloy.
An Investigation of Some Palladium-Titanium and Some Palladium-Titanium-Hydrogen Alloys
j. evans, i. r. harris and l. s. guzei, J. Less-Common Metals, 1979, 64, (2), P39–P57
Powdered and solid Pd-Ti alloys containing 0−30at.% Ti were investigated. The lattice spacings in the solid samples indicate a small progressive contraction of the Pd lattice on adding Ti, except for the range 7−14.5% Ti where the spacing remains constant. This region may be due to the compensatory effects of ordering and of adding Ti. Magnetic susceptibility measurements up to ∼9% Ti indicate Ti atoms have a valency of 4 in solutions of Pd. On hydrogenation Pd-Ti alloys containing 0−8.7% Ti were harder than the equivalent Pd-Ce solid solution alloys.
Superconducting and Normal State Properties of ErRh4B4 and LuRh4B4
l. d. woolf, d. c. johnston, h. b. mackay, r. w. mccallum and m. b. maple, J. Low Temp. Phys., 1979, 35, (5/6), 651–669
Heat capacity measurements of ternary compounds ErRh4B4 and LuRh4B4 were performed between 0.5 and 36K in magnetic fields up to 4kG, yielding new information on crystal field effects in these materials and on the influence of externally applied magnetic fields on the coupled superconducting-ferromagnetic reentrant transition in ErRh4B4. Static magnetic susceptibility data on LuRh4B4 are presented, and the electrical resistivity of ErRh4B4 was determined between 4K and room temperature.
The Effect of Trace Element Additions on the Grain Boundary Composition of Ir+0.3 Pct W Alloys
c. l. white, r. e. clausing and l. heatherly, Metall. Trans., 1979, 10A, (6), 683–691
The grain boundary fracture surfaces of several Ir+0.3%W alloys were examined by AES. Dopant additions (10−80 wt.ppm) of Th result in a Th enriched grain boundary of only a few atom layers thickness. The Th segregation inhibits grain boundary fracture during high temperature impact of the alloy, which is utilised for cladding radioactive fuel in radioisotope thermo-electric generators. (48 Refs.)
Experimental and Theoretical Study of Short Range Order in Ni-Os and Co-Os Alloys
a. a. katsnel’son, a. o. mekhrabov and v. m. silonov, Fiz. Metal. Metalloved., 1979, 47, (5), 993–997
X-ray analysis and a pseudopotential method were used to study the short range order in Ni-Os and Co-Os systems. It is shown that local short range order exists in Ni-1.5 at.% Os and Co-1.5, 1.3, 0.5 at.% Os alloys. The energy of ordering and the short range parameters were calculated.
Synthesis of Platinum(II) Tetraamine Complexes and Investigation of Molecular Electroconductivity of Their Aqueous Solutions
n. n. zheligovskaya, e. p. krasovskaya and l. v. popov, Vestnik Moskov. Univ., Ser. II Khim., 1979, 20, (3), 261–264
Mixed trans -tetraamine complexes of the following types were prepared and studied: [Pt(NH3)2Am2]Cl2 where Am is methylamine, ethyl amine, diethyl amine, etc., and also cis -[Pt(NH3Py4)2]Cl2 and [PtPy4]Cl2 where Py is pyridine. New trans -Pt(NH3)2(t-C4H9NH2)2Cl2 was obtained. The results showed that mobility of the complex cations decreased with the increase of the size of the amino ligands.
A Versatile Starting Material: Substitution Reactions of Bis(acetato)bis(diethyl sulfide)-platinum with Phosphines, Thiols, o-Hydroquinones and Dihydroxybenzoquinones
j. kuyper, Inorg. Chem., 1979, 18, (6), 1484–1489
A new compound cis -Pt(OAc)2(Et2S)2 has been prepared and used as a starting material in the synthesis of many new Pt complexes. Substitution reactions produced both cis -Pt(O-O)(Et2S)2 and cis -Pt(O2-O2)(Et2S)2 compounds. Other compounds synthesised by various stages were trans -Pt2(μ−(O2−O2))2(Et2S)4, Pt(SAr)2(EtS)2, [Pt(SAr)2]n, mono- and bis-substituted phosphine compounds and PtI2(Et2S)2, etc. Both the acetato or sulphide groups were readily substituted simultaneously or separately in high yield.
ESR and Optical Studies on the Interaction between cis -Dichlorodiammine Platinum(II) and Tryptophan
h. neubacher, p. zaplatynski, a. haase and w. lohmann, Z. Naturf. B, 1979, 34, (7), 1015–1018
cis -Dichlorodiammine Pt(II), which is known to be an active anti-tumour compound, and tryptophan form paramagnetic complexes in aqueous solution. These were detected by electron spin resonance spectroscopy (ESR) after a reaction time of several hours. The ESR spectra are due to Pt(III) in a low spin d7 configuration. The optical studies suggest columnar structures for the paramagnetic complexes.
Krypton and Xenon Inclusion Compounds of Complex Metal Cyanides
m. kämper, m. wagner and a. weiss, Angew. Chem. Internat. Ed. En., 1979, 18, (6), 486–487
The structure of CdPt(CN)6.1.046Kr and CdPt(CN)6.1.128Xe crystals were examined after synthesis. The host compound CdPt(CN)6 has space group Fm3m. These compounds have high stability and may provide a technically interesting alternative to the storage of gases in steel cylinders. In the Kr compound, Kr is present at a density corresponding to that of an ideal gas at 118 bar. If all the host lattice cavities, which are hydrophobic, are occupied by preparation at higher pressure this value rises to 216 bar.
The Effect of Iodide on the Electrochemical Reduction of Thick Oxide Films Formed on Platinum Electrodes in Sulfuric Acid Solution
s. shibata and m. p. sumino, J. Electroanal. Chem. Interfacial Electrochem., 1979, 99, (2), 187–195
The reduction of thick oxide films formed on Pt under severe anodic conditions was studied in the presence of adsorbed I−. A Pt electrode with a reduced superficial monolayer oxide on the thick oxide adsorbs I−. Iodide adsorbed on its surface blocks the adsorption of hydrogen and greatly slows down the cathodic reduction of the inner thick oxide remaining. The results showed that the reduction rate of the inner oxide depends only on the coverage by hydrogen, which coexists with adsorbed I−.
New Developments in Platinum Type Anodes
r. baboian, Mater. Performance, 1979, 18, (1), 9–15
Developments in Pt clad Nb anodes for cathodic protection in sea water, deep wells and underground are described. Low porosity of roll clad Pt-Nb and resistance of Nb to breakdown in chlorides at up to 120V improves sea water performance in drill rigs, heat exchanges and pipelines. Soil burial in carbonaceous backfill reduces Pt attrition because current is transferred from the Pt to the C where the anode reactions occur. Reinforced Pt clad Nb sheet or mesh anodes are used in sea water, deep wells and soils, while probe anodes are used in heat exchanges.
Electrochromism in Anodic Iridium Oxide Films. II. pH Effects on Corrosion Stability and the Mechanism of Coloration and Bleaching
s. gottesfeld and j. d. e. mcintyre, J. Electrochem. Soc., 1979, 126, (5), 742–750
The oxidation state of Ir ions in an oxide film, grown electrochemically and an Ir metal reflector electrode can be rapidly and reversibly modulated: Ir(OH)n(transparent)⇌IrOx(OH)n−x (blue-black). By suitable choice of electrolyte the colour-bleach process can occur without causing film growth on dissolution; in weakly acidic solutions the bleach rate is quick since H2O molecules in the film pores and/or H2O or OH groups provide protons at the oxide/electrolyte interface. This system has a broad spectral absorption, good contrast, fast response, good corrosion stability, useful for display devices.
Excited-State Photochemistry in the Tris(2, 2′-bipyridine)Ruthenium(II)Sulfite System
c. creutz, n. sutin and b. s. brunschwig, J. Am. Chem. Soc., 1979, 101, (5), 1297–1298
Three efficient photochemical methods for generation of Ru(bpy)+3 in aqueous solution are described. Both excited Ru(bpy)2+3 and Ru(bpy)+3 are excellent reducing agents and may be useful as mediators in photoproduction of secondary species capable of bringing about the rapid reduction of water to H2. Ru(bpy)+3 could be of greater practical value than excited Ru(bpy)2+3, because of its great reducing power and also because the back reaction is less favourable and so slower. The photolysis of Ru(bpy)2+3/Q solutions (Q=Eu2+aq, SO2−3, HA−) in the presence of possible H2 precusors is being examined.
Photoelectrochemical Production of Hydrogen from the Tris(2,2′-bipyridine)ruthenium-NN′-Dimethyl-4,4′-bibyridylium(Paraquat) System
ELECTRODEPOSITION AND SURFACE COATINGS
Obtaining Diffusion Heat-Resistant Coatings on Niobium
v. f. shatinski, v. v. drobit, m. s. goikhman and m. f. zamora, Zashchita Metal., 1979, 15, (3), 373–375
Diffusion heat resistant coatings on Nb alloys, prepared by diffusion metallisation from liquid Ca solution with 5 wt.% Pt, Re, Ge, etc. were studied in air at 800−1100°C. A linear dependence of the rate of oxidation on the temperature of Pt coated surfaces was obtained. Activation energy of the oxidation process was 14.8 kcal/mol for Pt. Kinetic mechanisms and oxidation parameters of multicomponent coatings, consisting of solid base Pt, Si, Cr containing carbide systems, are given.
Effect of Pt Ion Plating on the Creep Behavior of Alpha Ti
s. fujishiro and d. eylon, Scripta Metall., 1979, 13, (3), 201–203
Samples of Ti and Ti-5Al-2.5Sn were Pt ion plated to find its effect on the creep behaviour of the samples. Creep tests in air were performed. Bare or coated α-Ti wire exposed to air showed no difference in creep behaviour. It is thought that O2 induces transformation of phase boundary β to α phase with concurrent generation of additional mobile dislocations. However, ion plating may be effective in increasing air creep strength for Ti alloys containing the β phase, at test temperatures.
A Study of the Products of Ultraviolet Irradiation of Palladium-Containing Catalysts for Electroless Metal Deposition
b. k. w. baylis, c.–c. huang and m. schlesinger, J. Electrochem. Soc., 1979, 126, (3), 394–397
The effect of u.v. light on the Sn−Pd species used in electroless metal deposition using Sn(II) and Sn(IV) solutions as the sensitisers was studied. With irradiated Sn(IV)−Pd, less Pd was rinsed off during the post activation rinse than from the non-irradiated species, indicating that the light does not simply break the bonding attaching the Pd, allowing it to be rinsed off. When Sn(II) is the sensitiser more Pd seems to be found.
Evaluation of an Improved Ruthenium Plating Process
t. a. palumbo, Plating Surface Finish., 1979, 66, (8), 42–44
An improved Ru plating process was evaluated using a buffered acid solution of K3[Ru2N(H2O)2Cl8] in a small scale plating cell to plate reed contacts with a 1 μm layer of Ru over 1 μm of soft Au. The Ru electrolyte remained stable during evaluation and had a constant cathode efficiency. The Ru deposits were pure and had lower stresses and remained crack free after thermal shock testing. Ru is an excellent contact material. It is not attacked by hot or cold acids or aqua regia.
Automotive Exhaust Emissions Control Using the Three-Way Catalyst System. 1. Computer Simulation of the NO-H2-O2 Reaction on Pt/Al2O3 Catalyst
a. miyamoto, b. inoue and y. murakami, Ind. Eng. Chem., Prod. Res. Dev., 1979, 18, (2), 104–109
The kinetics of the NO−H2−O2 reaction on a Pt/Al2O3 catalyst were studied by a method of computer simulation. The calculations showed the existence of a space where all the NO, NH3, H2 and O2 can be removed simultaneously. NH3 played an important part as an intermediate in the reaction. Directions for the improvement of Pt/Al2O3 as a catalyst are suggested. The computer simulation was useful for the analysis of a complex system, such as the three-way catalyst system.
Production of 1-Naphthol on Rhenium-Platinum Catalysts
v. v. sobolev, d. a. sibarov, a. b. uglovoi and v. a. proskuryakov, Zh. Priklad. Khim., 1979 52, (1), 450–452
Studies of dehydrogenation of 1-tetralone on Re-Pt/γ−Al2O3, Pt/γ−Al2O3 and Re/γ−Al2O3 catalysts promoted with K2O were carried out in a flow reactor at 300−450°C. Re-Pt/γ−Al2O3 catalysts showed similar activity to the monometallic catalysts. The most active were 0.5% Re-0.2%Pt/γ−Al2O3 catalysts yielding 96% 1-naphthol for an 84% conversion of 1-tetralone at 375°C.
Reaction of Sulfur Oxides with Alumina and Platinum/Alumina
j. c. summers, Environ. Sci. Technol., 1979, 13, (3), 321–325
At temperatures >500°C, very little SO2 is adsorbed on Al2O3 in the absence of O2 and noble metals. With O2 present, significant quantities of SO2, above those occurring independently in the gas phase, are oxidised to SO3 and stored on the Al2O3. Pt enhances the SO2 storage rate on Al2O3. In the absence of O2, Pt appears to catalyse the disproportionation of SO2. With O2 present in the feedstream, Pt catalyses the oxidation of SO2. SO2 and SO3 adsorb on different Al2O3 sites, but SO3 adsorption does not affect the SO2 adsorption rate.
Palladium-Catalyzed Hydrogenation of Soybean Oil
m. m. ahmad, t. m. priestley and j. m. winterbottom, J. Am. Oil Chem. Soc., 1979, 56, (5), 571–577
The hydrogenation of soybean oil was studied using various Pd/C catalysts at H2 pressures between ambient and 70 psig and at temperatures from 80−160°C, and compared with commercial Ni catalysts. Pd catalysts with the metal on the exterior of the support were the most active and selective at ambient pressures. However, Pd catalysts with metal in the charcoal pore system were the most active at higher H2 pressures. Pd catalysts produced more trans-acids than Ni and the selectivity of Pd was superior to that of Ni and 15–20 times greater.
Catalysis by Supported Transition Metal Complexes. X. Study of Ionic Exchange and Role of Hydroxyl Groups on Palladium Resins
h. dupin, j. sabadie, d. barthomeuf and j. e. germain, Bull. Soc. Chim. Fr. I, 1979, (3/4), 86–90
The selectivity of Pd/resin catalysts, active after reduction of the liquid phase hydrogenation of allyl alcohol to propanol, is directly related to the density of OH− groups on the support with a maximum value of 80%. HCl addition decreased the selectivity to ∼50% while NaOH addition to the catalysts increased their selectivity in the same reaction to ∼75%. The support effect is therefore ascribed to the OH− groups left on the resin due to incomplete exchange with Pd salts.
Active States of Rhodium Exchanged Y Zeolite Catalysts for Hydrogenation of Ethylene and Acetylene and Dimerization of Ethylene Studied with X-Ray Photoelectron Spectroscopy
y. okamoto, n. ishida, t. imanaka and s. teranishi, J. Catalysis, 1979, 58, (1), 82–94
Rh-Y zeolite catalysts were investigated by X-ray photoelectron spectroscopy. Rh(I) was formed in Rh-Y zeolites as a significantly stable intermediate during the reduction of Rh(III) to Rh by heat treatment. The Rh(I) in Rh-Y zeolites was active for the hydrogenation and dimerisation of ethylene, whereas Rh metal was active for the hydrogenation of both ethylene and acetylene. Strong correlations were established between homogeneous Rh complex catalysts and Rh-Y catalysts both in the active oxidation states of Rh and in the effect of additives on the reactions.
Decomposition of Ammonia on Ru/Al2O3 Catalysts with Various Dispersities
d. v. sokol’skii, t. v. kuzora and a. b. farman, Zh. Priklad.Khim., 1979, 52, (4), 737–740
Studies of the decomposition reaction of NH3 on 3 wt.% Ru/Al2O3 catalysts with the grain sizes ranging from 0.05 to 3 mm were performed in a flow apparatus at 300−500°C. Diffusion inhibition was observed on samples with grain sizes of >1 mm at >400°C. Thus, activity of the catalyst and the activation energy increased due to only a small part of the surface being available.
Platinum-Diphosphine-Tin Systems as Active and Selective Hydroformylation Catalysts
y. kawabata, t. hayashi and i. ogata, J. Chem. Soc., Chem. Commun., 1979, (10), 462–463
The activity of the PtCl2(PPh3)2−SnCl2 complex as a hydroformylation catalyst was dramatically enhanced by the use of diphosphine ligands which were capable of forming a strained seven-membered chelate ring. The best ligand was trans –1,2–bis(diphenylphosphinomethyl) cyclobutane which gives hexanals (n/iso=99/1) from pent-1-ene with a much higher reaction rate than by the use of HRh(CO)(PPh3)3.
Chemistry of Metal Hydrides. XXIII. Catalytic Hydrogenation of Olefins Using trans- PtH(NO3)(PEt3)2 as Catalyst
h. c. clark, c. billard and c. s. wong, J. Organometal. Chem., 1979, 173, (3), 341–347
The catalyst trans -PtH(NO3)(PEt3)2 was found to be active for the hydrogenation of olefins. While it is active towards both internal and terminal olefins, it is not effective towards olefins with electron-withdrawing substituents. The hydrogenation is most effective when conducted in methanol at 60°C and 600 psi. The markedly enhanced activity of the catalyst in methanol compared with acetone or methylene chloride is discussed.
Potassium-Dinitrogen-Ruthenium Complex as an Active Catalyst for Nitrogen Fixation
a. ohya, k. urabe, k. aika and a. ozaki, J. Catalysis, 1979, 58, (2), 313–319
K uptake by Rh is enhanced and stabilised by the presence of N2, with a significant N2 uptake. The K uptake is stable, even during evacuation at 350°C and is stoichiometrically related to N22, suggesting that ternary compound (KN2Ru)n is formed. Electrical resistance of Ru film is decreased slightly by (KN2Ru)n. The K adsorbed increases the activity for the isotopic equilibration of N2. Evidence for the dinitrogen nature of the compound is supported by hydrazine, NH3 and a dinitrogen complex of Ru formed upon hydrolysis as well as ethanolysis.
Photoactivation and Photosensitisation of Homogeneous Hydrogenation Catalyst IrCl(CO)[P(i−C3H7)3]2
Solvent Extraction in Platinum Group Metal Processing
m. j. cleare, p. charlesworth and d. j. bryson, J. Chem. Technol. Biotechnol., 1979, 29, (4), 210–224
The various ways in which the chemistry of the platinum group metals (PGM) is manipulated to achieve separations using solvent extraction techniques is indicated. Mechanisms of solvent extraction processes are discussed and related to PGM complex chemistry. Potential economic advantages for solvent extraction over conventional precipitation processes are considered.
ELECTRICAL AND ELECTRONIC ENGINEERING
Characterization of Thick Film Compositions on Porcelain Steel Substrates
t. r. allington and r. e. cote, Solid State Technol., 1979, 22, (1), 81–86
Pt−Ag+Pd−Ag compositions were printed and fired onto porcelain steel substrates and tested for adhesion, ageing, solder leach resistance and resistivity. Ageing tests were normal and resistivity results are comparable to those observed on 96% Al2O3 substrates; adhesion remained constant after 1000 hours at 150°C. These results are comparable with other substrates; however, porcelainised steel while needing more research, promises to be suitable as a low cost, large size substrate for use in thick film circuitry.
Interdiffusion and Degradation of Si/Cr/Pt/Ag IMPATT Diode Metallization
s. d. mukherjee, d. v. morgan and m. j. howes, J. Electrochem. Soc., 1979, 126, (6), 1047–1053
Interdiffusion and degradation of Cr/Pt/Ag multiple metallisation layers for Si IMPATT diodes were studied. Grain boundary diffusion showed rapid initial growth and eventual saturation of solute Pt in Ag grains; and the effect of this on device failure caused by the possible depletion of the Pt barrier layer is discussed. Samples annealed in air showed substantial degradation of the Ag layer due to Cl2 contamination. The Cr/Pt interface was stable up to 400°C but annealing at or above 500°C caused mixing.
Low-Temperature Sintering of Pd/Ge Films on GaAs
h. r. grinolds and g. y. robinson, Appl. Phys. Lett., 1979, 34, (9), 575–577
Rectifying metal-semiconductor contracts, produced by heat treatment of a thin evaporated layer of Pd/Ge on n-type GaAs, were studied by Auger spectroscopy, X-ray diffraction and current-voltage measurements. During sintering at temperatures <350°C, Pd and Ge interdiffused on the non-reacting GaAs substrate forming PdGe and Pd2Ge. The form of the germanide phases altered the Ge LMM Auger spectra and produced an increase in the Schottky barrier energy from 0.67 to 0.85 eV. In general, sintered contracts have greater planar contact surface than alloy contacts.
Comparative Study of Chemical and Polarization Characteristics of Pd/Si and Pd/SiOx/Si Schottky-Barrier-Type Devices
l. l. tongson, b. e. knox, t. e. sullivan and s. j. fonash, J. Appl. Phys., 1979, 50, (3), 1535–1537
AES and ISS studies of the chemical nature of semitransparent (∼125Å) Pd/Si Schottky-barrier type devices were performed. Pd silicide was formed in the metal-semiconductor structures, while the presence of an ultrathin (∼30Å) purposely grown semiconductor oxide film inhibited the chemical reaction between Pd and Si in the metal overlayer. Chemical bonding information was correlated with barrier height.
cis-Platinum: A New Anticancer Agent
c. j. williams and j. m. a. whitehouse, Br. Med. J., 1979, 1, 1689–1691
A review of the drug platinum diamminodichloride (cisplatin) is presented, aimed at providing clinicians with information on the optimal methods of use, the toxicity and the anti-tumour effects of the drug.
Co-ordinate Compounds with Potential Anti-Tumour Activity. 1. Platinum and Palladium Complexes with Aminic Ligands
s. kirchner, c. drĂgulescu, a. maurer, v. topciu and n. csaki, Rev. Chim., 1979, 30, (4), 321–326
A number of complexes of Pt(II) and Pd(II) of the cis -dichlorodiammine type with hydrazine and organic cyclic saturated amines have been prepared, characterised and tested in vitro and in vivo for their anti-tumour activity. Two of the complexes, one of Pt(II) and one of Pd(II), tested on E coli B rods, led to deformed cells like methotrexate and exhibited quite good anti-tumour activity against Ehrlich ascites in a preliminary stage, but were almost inactive against advanced Ehrlich ascites.
Synthesis and Antimitogenic Activity of Some Co-ordination Compounds of Platinum(II), Palladium(II) and Rhodium(III)
a. vassilian, a. b. bikhazi and h. a. tayim, J. Inorg. Nucl. Chem., 1979, 41, (5), 775–778
Complexes of Pt(II), Pd(II) and Rh(III) with 2,6-diminopyridine and its 4-methoxy and 4-ethoxy derivatives were prepared and their antimitogenic activity was measured. Pt(II) complexes showed high antimitogenic activity and low toxicity. Pt(II) complexes were moderately active, while Rh(III) complexes enhanced thymidine uptake. The behaviour of Rh(III) complexes was of particular interest because such complexes may exhibit anti-tumour activity by enhancing the immune response of the system.
Age Hardening of Ag-Pd-Cu Dental Alloy
m. ohta, k. hisatsune and m. yamane, J. Less-Common Metals, 1979, 65, (1), P11–P21
The age-hardening characteristics of Au containing Ag-Pd-Cu dental alloys were investigated. Compositions examined were Ag 49.3−52.5 at.%, Pd 24.5−29.3 at.%, Cu 15.3−21.0 and Au 2.6−6.5 at.%. Hardening was found to be due to the precipitation of a CuPd ordered phase, with a AuCu-I type face centred tetragonal structure.