Alkyllithium-Initiated Polymerization of Trans-1,3,5-Hexatriene and Copolymerization with Styrene

1989 ◽  
Vol 62 (2) ◽  
pp. 332-342 ◽  
Author(s):  
Roderic P. Quirk ◽  
Rajeev Bhatia

Abstract The results reported herein established the complexity of the alkyllithium-initiated anionic homopolymerization, styrene copolymerization and styrene block copolymerization of 1,3,5-hexatriene in comparison to the controlled, predictable behavior observed with dienes. As a result of 1,6- and 1,2-enchainment, conjugated diene units are formed along the polymer backbone which can react with the living carbanionic centers to produce branched polymers as indicated in Equation (1). The general effect of solvent on microstructure, as indicated by infrared spectral analyses, is analogous to that of dienes in that 1,2-addition is increased in polar versus hydrocarbon solvents. The observation of branching reactions suggests that conjugated trienes may be useful as branching agents for copolymerizations or linking reactions analogous to the behavior of divinylbenzenes.

2019 ◽  
pp. 453-483
Author(s):  
Scott L. Murchie ◽  
Jean-Pierre Bibring ◽  
Raymond E. Arvidson ◽  
Janice L. Bishop ◽  
John Carter ◽  
...  

1956 ◽  
Vol 34 (9) ◽  
pp. 1163-1167 ◽  
Author(s):  
L. C. Vining ◽  
W. A. Taber

Candidin, the antifungal antibiotic produced by Streptomycesviridoflavus, has been isolated in crystalline form. Analyses and equivalent weight values best fit a molecular formula C46H75NO17. The substance is amphoteric and probably contains one carboxyl and one amino group. Infrared spectral evidence also indicates a polyhydroxylated structure, and the absorption in the visible region shows the presence of a conjugated heptaene chromophore. An additional conjugated diene elsewhere in the molecule is suggested by hydrogenation values and the absorption maximum at 228 mμ.


2019 ◽  
pp. 484-498
Author(s):  
Victoria E. Hamilton ◽  
Philip R. Christensen ◽  
Joshua L. Bandfield ◽  
A. Deanne Rogers ◽  
Christopher S. Edwards ◽  
...  

1967 ◽  
Vol 45 (21) ◽  
pp. 2501-2512 ◽  
Author(s):  
A. Zwierzak

A general synthetic procedure leading to cyclic hydrogen phosphites has been devised. The effect of solvent on the P==O and P—H infrared stretching modes of cyclic hydrogen phosphites and thiophosphites has been studied. It is concluded that association of cyclic hydrogen phosphites is attributable to dipole–dipole interactions rather than to hydrogen bonding.


2019 ◽  
pp. 413-427
Author(s):  
M. Cristina De Sanctis ◽  
Fabrizio Capaccioni ◽  
Eleonora Ammannito ◽  
Gianrico Filacchione

Icarus ◽  
2018 ◽  
Vol 301 ◽  
pp. 76-96 ◽  
Author(s):  
M.R. Salvatore ◽  
T.A. Goudge ◽  
M.S. Bramble ◽  
C.S. Edwards ◽  
J.L. Bandfield ◽  
...  

2019 ◽  
Vol 32 (3) ◽  
pp. 231-241
Author(s):  
Asma Iqbal ◽  
Humaira Masood Siddiqi ◽  
Maria Zubair ◽  
Toheed Akhter ◽  
O Ok Park ◽  
...  

A series of novel fluorescent co-polyimides are obtained by combining N 1-(4-aminophenyl)- N 1-(4-(benzo[ d]oxazol-2-yl) phenyl) benzene-1,4-diamine and 4,4′-oxydianiline with four aromatic anhydride, 3,3′,4,4′-benzophenonetetracarboxylic dianhydride, pyromellitic dianhydride, 4,4′-oxydiphthalic anhydride, and 4,4 ′-(hexafluoroisopropylidene)diphthalic anhydride following conventional polycondensation method. The resultant co-polyimides are characterized by elemental, Fourier transform infrared spectral analysis and gel permeation chromatography. All newly prepared polyimides (PIs) exhibit shallow highest occupied molecular orbital energy levels in the range of −4.47 to −4.98 eV and have reasonable optical bandgaps. The photoluminescence spectral analysis shows blue to green emission in solution form. Thermal and solubility properties reveal that the PIs with pendant 4-(benzo[ d]oxazol-2-yl group linked to triphenylamine unit in polymer backbone impart not only good thermal stability but also appreciable solubility making these new co-polyimides versatile for multipurpose usage.


1988 ◽  
Vol 33 (2) ◽  
pp. 395-399 ◽  
Author(s):  
J. Čejka ◽  
Z. Urbanec ◽  
J. Čejka ◽  
J. Ederová ◽  
A. Muck

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