Show/Hide Menu
Hide/Show Apps
Logout
Türkçe
Türkçe
Search
Search
Login
Login
OpenMETU
OpenMETU
About
About
Open Science Policy
Open Science Policy
Open Access Guideline
Open Access Guideline
Postgraduate Thesis Guideline
Postgraduate Thesis Guideline
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
DIPOLE-MOMENTS OF COPOLYMERS IN RELATION TO THE DISTRIBUTION OF POLAR MONOMER UNIT SEQUENCES
Date
1991-01-01
Author
KUCUKYAVUZ, Z
BAYSAL, BM
Metadata
Show full item record
This work is licensed under a
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License
.
Item Usage Stats
197
views
0
downloads
Cite This
A method for evaluating the dipole moments of copolymers in relation to the distribution of polar unit sequences is proposed. Experimental data on the synthesis and dipole moments of styrene-p-chlorostyrene and styrene-p-methoxystyrene copolymers were used to calculate the effective dipole moment of a polar unit in a copolymer. For this purpose, we assumed the following effective moment values for the corresponding polar unit sequences along the copolymer chains: when both of the nearest neighbours are polar, mu(PP), when one of the nearest neighbours is polar and the other is non-polar, mu(PS), and when both of the nearest neighbours are non-polar, mu(SS). The relative magnitudes of mu(SS), mu(PS) and mu(PP) calculated for both copolymers reflect the influence of dipole-dipole interactions on the effective dipole moment of a polar unit in a copolymer molecule.
Subject Keywords
Organic Chemistry
,
Polymers and Plastics
URI
https://hdl.handle.net/11511/65036
Journal
POLYMER
DOI
https://doi.org/10.1016/0032-3861(91)90547-v
Collections
Department of Chemistry, Article
Suggestions
OpenMETU
Core
Understanding the influence of hydrogen bonding and diisocyanate symmetry on the morphology and properties of segmented polyurethanes and polyureas: Computational and experimental study
Sami, Selim; Yıldırım, Erol; Yurtsever, Mine; Yurtsever, Ersin; Yilgor, Emel; Yilgor, Iskender; Wilkes, Garth L. (Elsevier BV, 2014-09-02)
Quantum mechanical calculations (QMC) and dissipative particle dynamics (DPD) siniulations were utilized to understand the nature of the short and long-range hydrogen bonding and its influence on the microphase morphology in segmented polyurethanes and segmented polyureas prepared without chain extenders through the stoichiometric reactions of hydroxy or amine terminated poly(tetramethylene oxide) (PTMO-1000) with 1,4-phenylene diisocyanate (PPDI) and 1,3-phenylene diisocyanate (MPDI). The possibility of lo...
ELECTROINITIATED POLYMERIZATION OF HALOPHENOLS - ELECTROINITIATION POTENTIAL LUMO RELATIONS
TURKER, L; KISAKUREK, D; SEN, S; Toppare, Levent Kamil; Akbulut, Ural (Wiley, 1988-11-01)
Electroinitiated polymerizations can be carried out by direct electron transfer via constant potential electrolysis.1–3 In doing so, the anodic (Ep, a) and the cathodic (Ep, c) potentials of the monomers must be measured by cyclic voltammetry. The cathodic peak potentials of halophenols were measured on Pt0 electrode versus Ag0/Ag+ in acetonitrile. Electroinitiated polymerization of bis(pyridine), bis(4‐chloro‐2,6‐dibromophenoxide) copper (II) complex was studied in dimethylformamide‐tetrabutylammonium flu...
Electrochemical polymerisation of 2-aminofluorene in ethylalcohol/water medium
Imamoglu, T; Önal, Ahmet Muhtar (Elsevier BV, 2004-08-01)
Electrochemical polymerisation of 2-aminofluorene, 2AF, was investigated in ethylalcohol/water mixture (3:2, v:v) in the presence of HClO4 as the supporting electrolyte via constant potential electrolysis, CPE. Prior to CPE, electrochemical behaviour of the monomer was investigated in the same solvent electrolyte couple utilising cyclic voltammetry, CV. Electrochemical polymerisation of the monomer yielded insoluble, dark bluish-green, conducting polymer deposit on the electrode surface. Characterisation of...
Kinetic study of the reaction between hydroxyl-terminated polybutadiene and isophorone diisocyanate in bulk by quantitative FTIR spectroscopy
Kincal, D; Özkar, Saim (Wiley, 1997-12-05)
A kinetic study of the reaction between a hydroxyl-terminated polybutadiene (HTPB) and isophorone diisocyanate (IPDI) was carried out in the bulk state by using quantitative Fourier transform infrared(FTIR) spectroscopy. The reaction is shown to obey a second-order rate law, being first order in both the HTPB and IPDI concentrations. The activation parameters obtained from the evaluation of kinetic data are Delta H-double dagger = 41.1 +/- 0.4 kJ mol, Delta S-double dagger = -198 +/- 2 J K-1 mol(-1) and E-a...
A new soluble conducting polymer and its electrochromic devices
YİLDİZ, UMİT HAKAN; SAHİN, ELİF; Akhmedov, IM; Tanyeli, Cihangir; Toppare, Levent Kamil (Wiley, 2006-04-01)
A new polythiophene derivative was synthesized by both chemical and electrochemical oxidative polymerization of 1-(1-phenylethyl)-2,5-di(2-thienyl)-1H-pyrrole (PETPy). Of which the chemical method produces a polymer that is completely soluble in organic solvents. The structures of both the monomer and the soluble polymer were elucidated by nuclear magnetic resonance (H-1 and C-13 NMR) and Fourier transform infrared (FTIR) spectroscopy. The average molecular weight has been determined by gel permeation chrom...
Citation Formats
IEEE
ACM
APA
CHICAGO
MLA
BibTeX
Z. KUCUKYAVUZ and B. BAYSAL, “DIPOLE-MOMENTS OF COPOLYMERS IN RELATION TO THE DISTRIBUTION OF POLAR MONOMER UNIT SEQUENCES,”
POLYMER
, pp. 3418–3421, 1991, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/65036.