THE INTERACTION OF HYDRAZINE WITH BORON AND ALUMINUM HALIDES

1963 ◽  
Vol 41 (8) ◽  
pp. 1872-1876 ◽  
Author(s):  
W. G. Paterson ◽  
M. Onyszchuk
Keyword(s):  
Polymeric Material ◽  
Empirical Formula ◽  
Reaction Scheme ◽  
Hydrogen Halide ◽  
Polymeric Product ◽  
Boron Halides ◽  
Aluminum Halides

The interaction of boron halides BX3 (where X is Cl or Br) or aluminum halides Al2X6 (where X is Cl, Br, or I) with hydrazine is characterized by the elimination of hydrogen halide and the formation of substances with boron– (or aluminium–) nitrogen linkages. The hydrogen halide appears in the products as hydrazine hydrohalide, which can be separated by a hydrazine washing technique, leaving a polymeric material with empirical formula MN4H5 (where M is Al or B). A reaction scheme is proposed and possible structures of this polymeric product are discussed.

Etude des dérivés sulfohydroxylés des halogénures de bore et des cycles dérivés du borsulfol I. Synthèses et mécanismes réactionnels

1973 ◽  
Vol 51 (2) ◽  
pp. 292-301 ◽  
Author(s):  
Jean Bouix ◽  
Roger Hillel
Keyword(s):  
Hydrogen Halide ◽  
Boron Halides

By the action of H2S on boron halides (other than fluoride) one obtains the new substitution products BX2SH, BX(SH)2, and B(SH)3 along with the corresponding hydrogen halide. These halogenosulfhydroboranes are unstable and cyclize to cyclic boron sulfides, either (BSSH)3 or (BSX)3.In the case of boron bromide it is possible, by controlling the ratio of the reactants and the temperature of the reaction, to promote the formation of one of the three possible substitution products. Then by encouraging cyclization one may obtain, rapidly and selectively, either (BSSH)3 or (BSBr)3.Synthesis of (BSCl)3 was accomplished by dissolution of (BSSH)3 in liquid BCl3 and that of (BSI)3 by the action of H2S on solid BI3. [Journal translation]

Organic Syntheses During the Impact of a Comet with a Gaseous Planet

1997 ◽  
Vol 161 ◽  
pp. 189-195
Author(s):  
Cesare Guaita ◽  
Roberto Crippa ◽  
Federico Manzini
Keyword(s):  
Polymeric Material ◽  
Molecular Form ◽  
Parent Compound ◽  
Blue Filter ◽  
Organic Syntheses ◽  
The Impact

AbstractA large amount of CO has been detected above many SL9/Jupiter impacts. This gas was never detected before the collision. So, in our opinion, CO was released from a parent compound during the collision. We identify this compound as POM (polyoxymethylene), a formaldehyde (HCHO) polymer that, when suddenly heated, reformes monomeric HCHO. At temperatures higher than 1200°K HCHO cannot exist in molecular form and the most probable result of its decomposition is the formation of CO. At lower temperatures, HCHO can react with NH3 and/or HCN to form high UV-absorbing polymeric material. In our opinion, this kind of material has also to be taken in to account to explain the complex evolution of some SL9 impacts that we observed in CCD images taken with a blue filter.

Time-Resolved Cryo-Electron Microscopy of Oscillating Microtubules

1990 ◽  
Vol 48 (1) ◽  
pp. 502-503
Author(s):  
Eva-Maria Mandelkow ◽  
Ron Milligan
Keyword(s):  
Electron Microscopy ◽  
Dynamic Instability ◽  
Entire Solution ◽  
Reaction Scheme ◽  
Time Resolved ◽  
X Ray ◽  
X Ray Scattering ◽  
A Chain ◽  
Ray Scattering

Microtubules form part of the cytoskeleton of eukaryotic cells. They are hollow libers of about 25 nm diameter made up of 13 protofilaments, each of which consists of a chain of heterodimers of α-and β-tubulin. Microtubules can be assembled in vitro at 37°C in the presence of GTP which is hydrolyzed during the reaction, and they are disassembled at 4°C. In contrast to most other polymers microtubules show the behavior of “dynamic instability”, i.e. they can switch between phases of growth and phases of shrinkage, even at an overall steady state [1]. In certain conditions an entire solution can be synchronized, leading to autonomous oscillations in the degree of assembly which can be observed by X-ray scattering (Fig. 1), light scattering, or electron microscopy [2-5]. In addition such solutions are capable of generating spontaneous spatial patterns [6].In an earlier study we have analyzed the structure of microtubules and their cold-induced disassembly by cryo-EM [7]. One result was that disassembly takes place by loss of protofilament fragments (tubulin oligomers) which fray apart at the microtubule ends. We also looked at microtubule oscillations by time-resolved X-ray scattering and proposed a reaction scheme [4] which involves a cyclic interconversion of tubulin, microtubules, and oligomers (Fig. 2). The present study was undertaken to answer two questions: (a) What is the nature of the oscillations as seen by time-resolved cryo-EM? (b) Do microtubules disassemble by fraying protofilament fragments during oscillations at 37°C?

Making Graphene-type Material via Polymerization of Porphyrin

2020 ◽  
Author(s):  
SANJIB KAR ◽  
Sruti Mondal ◽  
Kasturi Sahu ◽  
Dilruba Hasina ◽  
Tapobrata Som ◽  
...  
Keyword(s):  
Layer Thickness ◽  
Polymeric Material ◽  
Single Layer ◽  
Type Material ◽  
Synthetic Pathway ◽  
Simple Chemical ◽  
Doped Graphene ◽  
Ring Nitrogen ◽  
2D Structure ◽  
Porphyrin Macrocycles

<p>The synthesis of new graphene-type materials (<i>via</i> polymerization of porphyrin macrocycles) through a simple chemical synthetic pathway (at RT) has been demonstrated. This newly synthesized material can be dispersed in water with an average sheet size of few microns and with single layer thickness. As the porphyrin contains four inner ring nitrogen atoms thus the presented polymeric material will be close analogous of N-doped graphene. Porphyrin as the key component to synthesize layered graphene type continuous 2D structure has never been attempted before. </p> <p> </p>

Influence of free convection on the diffusion current to a sphere in a laminar forced flow regime

1985 ◽  
Vol 50 (12) ◽  
pp. 2697-2714
Author(s):  
Arnošt Kimla ◽  
Jiří Míčka
Keyword(s):  
Asymptotic Expansion ◽  
Free Convection ◽  
Boundary Value Problem ◽  
Concentration Gradient ◽  
Empirical Formula ◽  
Convective Diffusion ◽  
Forced Flow ◽  
Diffusion Current ◽  
Wide Range ◽  
Free And Forced Convection

The formulation and solution of a boundary value problem is presented, describing the influence of the free convective diffusion on the forced one to a sphere for a wide range of Rayleigh, Ra, and Peclet, Pe, numbers. It is assumed that both the free and forced convection are oriented in the same sense. Numerical results obtained by the method of finite differences were approximated by an empirical formula based on an analytically derived asymptotic expansion for Pe → ∞. The concentration gradient at the surface and the total diffusion current calculated from the empirical formula agree with those obtained from the numerical solution within the limits of the estimated errors.

The mechanism of the anionic coordination polymerization of isoprene

1980 ◽  
Vol 45 (9) ◽  
pp. 2391-2399 ◽  
Author(s):  
Miroslav Kašpar ◽  
Jiří Trekoval
Keyword(s):  
Chromatographic Method ◽  
Initial Period ◽  
Reaction Scheme ◽  
Polymerization Kinetics ◽  
Coordination Polymerization ◽  
Initial Concentration ◽  
The Cross ◽  
Gas Chromatographic Method ◽  
Kinetics Of

The polymerization kinetics of isoprene (2-methyl-1,3-butadiene) in benzene with butyllithium as the initiator was investigated by the gas chromatographic method. After completion of the initial period of the reaction, its order with respect to the initial concentration of initiator is negative at the concentrations of the latter between 0.01 and 0.25 mol/l, and positive at higher concentrations. A reaction scheme has been suggested with respect to the "cross" association of butyllithium and of the "living" oligoisoprene.

Oxidation scheme of symmetrically disulphonated naphthidines with cerium(IV) sulphate

1981 ◽  
Vol 46 (3) ◽  
pp. 561-572 ◽  
Author(s):  
Karel Komers
Keyword(s):  
Sulphuric Acid ◽  
Rate Constants ◽  
Oxidation Product ◽  
Side Reaction ◽  
Reaction Scheme ◽  
Second Order ◽  
Intermediate Products ◽  
Stable Intermediate ◽  
Starting Compound ◽  
Oxidation Agent

The author derived theoretical dependences of preasymptotic slopes of the currentless E-t curves (potential of an indicator redox electrode against time) on the number of equivalents, n, of added oxidation agent, assuming a reaction scheme of two consecutive concurrent second-order reactions involving the formation of intermediate products ( a side reaction of the starting compound with the final oxidation product leading to an adduct, which undergoes consecutive bimolecular oxidations leading again to the final product). The dependences enable to determine the type of the relatively stable intermediate products and the ratios of the rate constants. The theory was applied to the oxidation of four symmetrically disulphonated naphthidines with cerium(IV) sulphate in aqueous sulphuric acid and the results were substantiated spectrophotometrically

The effect of electrondonors on the polymerization kinetics of isoprene

1980 ◽  
Vol 45 (12) ◽  
pp. 3338-3346
Author(s):  
Miroslav Kašpar ◽  
Jiří Trekoval
Keyword(s):  
Induction Period ◽  
Ethyl Ether ◽  
Reaction Order ◽  
Propagation Rate ◽  
Reaction Scheme ◽  
Polymerization Kinetics ◽  
Polymerization Rate ◽  
Constant Concentration ◽  
Initial Concentration ◽  
Kinetics Of

The effect of small additions of 1-octene, butyl ethyl ether and triethylamine on the polymerization kinetics of isoprene (2-methyl-1,3-butadiene) in benzene initiated with butyllithium was investigated by employing the GLC analysis. The addition of 1-octane was reflected only in a shorter induction period of the reaction; the effect on the propagation rate was insignificant. With the increasing amount of butyl ethyl ether, the polymerization rate increases linearly, while the reaction order with respect to the concentration of triethylamine is variable and increases from 0.33 to 0.66 with the increasing concentration of the initiator. For a constant concentration of triethylamine, the reaction order with respect to the initial concentration of the initiator was found to vary considerably, reaching even negative values. A reaction scheme was suggested, taking into account the competition between two different solvates of alkyllithium.

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