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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    European journal of pediatrics 124 (1977), S. 179-183 
    ISSN: 1432-1076
    Keywords: 13-trisomy ; Microphthalmia ; Coloboma ciliary body ; Cataracts ; Retinal detachment ; Retinal dysplasia ; Proliferation of pigment epithelium ; Calcified drusen ; Fibrocartilaginous dysplasia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The gross and microscopic eye findings in the first historic case of the 13-trisomy syndrome included: severe microphthalmia, coloboma of the ciliary body, cataracts, detached retina, and retinal dysplasia.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 901-908 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Improvements in the 13C NMR Grant and Paul parameters as applied to polymers have been obtained by noting that the “corrective terms” can be temperature-sensitive. A corresponding temperature sensitivity was not observed for the primary parameters, α through ∊. Results are given for a hydrogenated polybutadiene and six different ethylene-1-olefin copolymers where the standard deviation between calculated and observed chemical shifts has been improved from 1.04 to 0.30 ppm. Since the “corrective terms” in the Grant and Paul empirical analyses of chemical shifts reflect the conformational character of polymers, it is shown that values for these terms can best be obtained directly from the system under study.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 14 (1976), S. 1693-1700 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Spin-lattice relaxation times (T1) for methyl, methylene, and methine carbons in an amorphous polypropylene have been measured as a function of temperature from 46 to 138°C. The carbons from isotactic sequences characteristically exhibited the longest T1's of those observed. The T1 differences increased with temperature with the largest difference occuring for methine carbons where a 32% difference was observed. Activation energies were determined for the motional processes affecting T1's for isotactic and syndiotactic sequences with essentially no dependence upon configuration noted.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 1975-1990 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The 1,4-1,2 additions in three hydrogenated polybutadienes are described in terms of triads of monomer units, average sequence lengths, and branches per 1000 carbon atoms. A test for conformity with Markov statistical behavior shows that the measured triad distributions can be closely reproduced assuming a first-order model. Transition probabilities from the statistical analysis can be used to calculate the relative concentration of any desired sequence. Steric factors during polymerization may lead to the first-order bias in the monomer distribution.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 13 (1975), S. 889-899 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 13C NMR configurational assignments are made for an amorphous polystyrene sample examined at 25.2 MHz and 120°C. The assignments are based strictly on a one-parameter Bernoullian fit that was in satisfactory agreement with the nine observed methylene relative intensities. The methylene regions of the 13C NMR spectra of a polystyrene were examined before and after hydrogenation of the side-chain phenyl substituents. It was concluded that ring current effects have influenced the 13C methylene chemical shifts substantially and are limited largely to contributions from adjacent phenyl substituents. In addition, aromatic substituent parameters are reported that can be used in conjunction with the Grant and Paul parameters for calculating chemical shifts in aromatic hydrocarbons and polymers. Finally, it is concluded that free-radical and n-butyllithium-prepared polystyrenes have essentially atactic structures with meso additions favored over racemic additions by approximately 55/45.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 14 (1976), S. 2083-2094 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Sequence lengths of stereochemical additions in vinyl polymers are described in terms of the number average lengths of like configurational placements. Under these circumstances, a pure syndiotactic polymer has a number average sequence length of 1.0; a polymer with 50:50 meso, racemic additions has a number average sequence length of 2.0 and polymers with more meso than racemic additions have number average sequence lengths greater than 2. Amorphous and crystalline polypropylenes and an amorphous polystyrene are examined using 13C NMR as examples of the applicability of the average sequence length method. The results appear to be accurate for amorphous and semicrystalline polymers but limitations are present when this method is applied to highly stereoregular vinyl polymers containing predominantly isotactic sequences.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 15 (1977), S. 1451-1473 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Monomer distributions and number-average sequence lengths are determined from 13C nuclear magnetic resonance (NMR) data for 1,4- and 1,2-butadiene additions and styrene additions in a series of four hydrogenated butadiene-styrene copolymers. The monomer distribution is expressed in terms of the six unique days from which it is possible to calculate the number-average sequence length of each monomer type. Carbon-13 NMR spectral assignments are given and the techniques for making the assignments are discussed. The method presented could, in principle, be applied to any copolymer or terpolymer. Limitations that are encountered in the analysis of hydrogenated butadiene-styrene copolymers high in 1,2 additions are discussed.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 17 (1979), S. 2555-2565 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The following criteria are proposed to judge whether a coordination polymerization may be diffusion controlled or not: (1) If the number-average molecular weight and polydispersity of the polymer calculated from kinetic rate constants as a function of time agree with the experimental values, the polymerization is not diffusion controlled. (2) The polymerization may be diffusion controlled if the Thiele modulus, the ratio of the characteristic diffusion time to the characteristic reaction time, is much greater than unity; if it is much smaller than unity, the polymerization is reaction controlled. (3) If an initial linear dependence of rate of polymerization on catalyst concentration changes over to a square-root dependence, the polymerization may be diffusion limited. (4) The polymerization is likely to be diffusion limited if the instantaneous rate of polymerization is proportional to the rate of particle growth when the proportionality coefficient is the surface area of the particle. Criterion (1) is a necessary and sufficient condition as stated, as its converse is not true. All the other criteria are merely necessary but not sufficient conditions. The established Ziegler-Natta catalysts have activities too low to cause diffusion limitation; the Phillips catalyst system is likely to be diffusion limited. The polydispersity of polyolefins produced with Ziegler-Natta catalysts are not the consequence of diffusion control but are the characteristics of the catalysts in their kinetics of initiation, propagation, chain transfer, and termination.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 14 (1976), S. 1915-1932 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Tetrabenzyltitanium (B4Ti), tribenzyltitanium chloride (B3TiCl), tetra(p-methylbenzyl)titanium (R4Ti) and tri(p-methylbenzyl)titanium chloride (R3TiCl) have been used as catalysts for ethylene and propylene polymerization activated by AlEt2Cl. B4Ti-AIEt2Cl in solution polymerizes ethylene readily but its activity decays rapidly. B4Ti was also supported on Cab-O-Sil, Alon C, and Mg(OH)Cl. The last support was found to give catalyst with longest lifetime with a rate of polymerization, Rp = 7.0 g/hr-mmole Ti-atm ethylene. 14CO counting techniques gave 1.13 × 10-3 mole of propagating center per mole of B4Ti; the rate constant of propagation, kp = 540 l./mole-sec. None of the tetravalent titanium compounds polymerize propylene in solution. However, when supported on Mg(OH)Cl, Cab-O-Sil, Alon C, Cab-O-Ti, and charcoal, they all polymerize propylene. In this work the supports were characterized by various techniques, including the paramagnetic probe method, to determine the concentration and nature of surface hydroxyls. Those factors controlling the rate and stereospecificity of propylene polymerization were investigated. The system B3TiCl-Mg(OH)Cl-AlEt2Cl is the most active with Rp = 2.89 g/hr-mmole Ti-atm propylene. The concentration of propagation center is 0.9 × 10-3 mole per mole of B3TiCl; kp = 32 l./mole-sec. This catalyst gave only about 70% stereoregular polymer. Diethyl ether is found to raise stereospecificity to 100%, but there is a concommittent tenfold decrease of activity. Other interesting catalyst systems are: (π-C5H5)TiMe3-Mg(OH)Cl-AlEt2Cl (1.56, 89.5); (π-C5H5)TiMe2-Mg(OH)Cl-AlEt2Cl (0.075, 94.5); and (π-C5H5)TiMe3-Alon C-Al-Et2Cl (0.08,97.2), where the first number in the parenthesis is Rp in g/mmole Ti-hr-atm and the second entry corresponds to percentage yield of stereoregular polypropylene. Hafnocene and titanocene supported on Mg(OH)Cl produce only oligomers of propylene.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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