Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Communities & Collections
Communities & Collections
Help
Help
Frequently Asked Questions
Frequently Asked Questions
Guides
Guides
Thesis submission
Thesis submission
MS without thesis term project submission
MS without thesis term project submission
Publication submission with DOI
Publication submission with DOI
Publication submission
Publication submission
Supporting Information
Supporting Information
General Information
General Information
Copyright, Embargo and License
Copyright, Embargo and License
Contact us
Contact us
POLYMERIZATION OF MONOISOCYANATES BY THE PRUITT-BAGGETT ADDUCT
Date
1993-12-01
Author
YILMAZ, O
Usanmaz, Ali
ALYURUK, K
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
79
views
0
downloads
Cite This
n-Butyl isocyanate (nBIC) was polymerized in bulk by the Pruitt-Baggett adduct (PBA) at -23, 0.0, and 25.0-degrees-C. Polymerization was accompanied by trimerization to the cyclic isocyanurates at all temperatures. Spectroscopic evidences supported the nylon-1 structure for both trimer and polymer. The polymer /trimer ratio and the molecular weight of produced polymers were found to increase with decreasing temperature. The Pruitt-Baggett catalyst (PBC), which is the reaction product of (PBA + H2O) system, also polymerized nBIC, but with a relatively slower rate. In aromatic and etheric solutions, nBIC was only trimerized by PBA. Copolymerization of nBIC with propylene oxide by PBA and PBC failed. Some selected monoisocyanates were also polymerized by PBA. (C) 1993 John Wiley & Sons, Inc.
Subject Keywords
Organic Chemistry
,
Materials Chemistry
,
Polymers and Plastics
URI
https://hdl.handle.net/11511/51666
Journal
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
DOI
https://doi.org/10.1002/pola.1993.080311306
Collections
Graduate School of Natural and Applied Sciences, Article
Suggestions
OpenMETU
Core
Polymerization of propylene oxide by the Pruitt-Baggett catalyst
Çolak, Nureddin; Alyürük, Kemal (Elsevier BV, 1989-9)
The Pruitt-Baggett adduct (PBA) which formed from the reaction of FeCl3 with propylene oxide (PO) was hydrolysed in diethyl ether (ether) solutions at different mole ratios. Although the hydrolysates were insoluble in ether they could be converted into PO-soluble form (PBC) by a thermal treatment providing that the r value was kept smaller or equal to unity. PBC polymerized PO concurrently into a mixture of high molecular weight crystalline polymer with low molecular weight non-crystallizable oligomers. Th...
Monomer-bound ion pairs in the stereoregular polymerization of propylene oxide by the Pruitt-Baggett catalyst
Aksoy, S.; Altinok, H.; Tümtürk, H.; Alyürük, K. (Elsevier BV, 1990-6)
The Pruitt-Baggett adduct (PBA) (MW = 438 g mol−1) that formed from the reaction of FeCl3 with propylene oxide (PO) was hydrolysed in diethyl ether (ether) solutions at different molar ratios. The hydrolysates (), which were insoluble in ether, could be converted into catalytically active form () by a thermal treatment. was soluble in etheric solvents and in pyridine. These solutions, in contrast to PBA and , were electrical conductors. Profound differences in the electrical conductivity of was observed ...
POLYMERIZATION OF BIS(4-BROMO-2,6-DICHLOROPHENOXO) ETHYLENEDIAMINE COPPER(II) COMPLEX BY ELECTRO-INITIATION
KISAKUREK, D; YIGIT, S (Elsevier BV, 1991-01-01)
Bis(4-bromo-2,6-dichlorophenoxo) ethylenediamine copper(II) complex has been polymerized using electro-initiation by constant potential electrolysis, in dimethylformamide-tetrabutylammonium fluoroborate solvent-supporting electrolyte couple, at room temperature under air or N2. The process leads to low molecular weight (5.6 x 10(3)) linear poly(dichlorophenylene oxide). The structures of the polymers were determined by H-1-NMR and C-13-NMR. The kinetics of the polymerization were followed by in situ cycl...
Crosslinked polymer gels for boron extraction derived from N-glucidol-N-methyl-2-hydroxypropyl methacrylate
Bicak, N; Ozbelge, HO; Yılmaz, Levent; Senkal, BF (Wiley, 2000-03-24)
Glycidyl methacrylate was reacted in 2-methyl pyrrolidone solution with N-methyl-D-glucamine (NMG) to produce N-D-glucidol, N-methyl-2-hydroxy propyl methacrylate (GMHP). The reaction proceeded exclusively via ring opening of the oxirane. The resulting vinyl monomer was a waxy product and soluble in water, ethanol, methanol, DMF, and NMP. Copolymerization of GMHP with N,N'-tetraallyl piperazinium dichloride by the inverse suspension method (water in oil), using a toluene/chloroform (3:1) mixture as continuo...
Polymerization of propylene oxide and copolymerization of carbon disulphide and propylene oxide with xanthate salts
Aksoy, S.; Balkan, M.; Alyürük, K. (Elsevier BV, 1989-1)
Anionic polymerization of propylene oxide (PO) using several xanthate salts was studied. Low molecular weight oily polymers with variable sulphur content were obtained by using either potassium ethyl xanthate or potassium benzyl xanthate. The highest attainable conversion of PO was limited to ca 10%. The polymerization was accompanied by formation and precipitation of a by-product salt. In the presence of CS2, an oily copolymer with about 40% sulphur was obtained from the above mixtures. In reaction systems...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
O. YILMAZ, A. Usanmaz, and K. ALYURUK, “POLYMERIZATION OF MONOISOCYANATES BY THE PRUITT-BAGGETT ADDUCT,”
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
, pp. 3205–3211, 1993, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/51666.