Synthesis and Characterization of Coumarin–Trioxane–Urea Copolymers

1996 ◽  
Vol 8 (2) ◽  
pp. 295-300 ◽  
Author(s):  
D I Brahmbhatt ◽  
B R Hirani
Keyword(s):  
Molecular Weight ◽  
Elemental Analysis ◽  
Average Molecular Weight ◽  
Synthesis And Characterization ◽  
Number Average Molecular Weight ◽  
Molar Ratios

4-methyl-7-hydroxycoumarin trioxane urea (MHCTU) copolymers were prepared by copolycondensation of 4-methyl-7 hydroxycoumarin (MHC), trioxane (T) and urea (U) in the presence of 2 M HCl/H2SO4 as a catalyst with different molar ratios of reacting monomers. The copolymers were characterized by elemental analysis, IR spectral and TGA studies. The number average molecular weight ( Mn) of all the produced copolymers was determined by non-aqueous titrimetry.

Synthesis and characterization of poly(coumarin-urethane)s

1994 ◽  
Vol 6 (3) ◽  
pp. 257-262
Author(s):  
D I Brahmbbatt ◽  
L Jayabalan ◽  
Harshad D Patel
Keyword(s):  
Molecular Weight ◽  
Elemental Analysis ◽  
Vapour Pressure ◽  
Condensation Reaction ◽  
Average Molecular Weight ◽  
Spectral Studies ◽  
Synthesis And Characterization ◽  
Molecular Weight Determination ◽  
Number Average Molecular Weight

Poly(coumarin-urethane)s (PCUs) were prepared by the condensation reaction of 3,3'-dihydroxy-6,6'-methylcnebiscoumarin (DHMBC) with various diisocyanates. All the poly(coumarin-urethane)s were characterized by elemental analysis, IR spectral studies, number average molecular weight determination (by vapour pressure osmometry), viscosity studies and thermogravimetry.

scholarly journals Synthesis and Characterization of Colored Polyureas

2004 ◽  
Vol 1 (1) ◽  
pp. 51-56 ◽  
Author(s):  
M. G. Patel ◽  
K. R. Desai ◽  
H. S. Patel
Keyword(s):  
Electrical Conductivity ◽  
Molecular Weight ◽  
Room Temperature ◽  
Average Molecular Weight ◽  
Conductometric Titration ◽  
Spectral Studies ◽  
Synthesis And Characterization ◽  
Disperse Dyes ◽  
Number Average Molecular Weight

Various disperse dyes based onm-phenylenediamine have been prepared. These dyes then polycondensation with 4,4'-Diphenyl methane diisocyanate. The resultant colored polyureas were characterized by N content, IR spectral studies, Number Average Molecular Weight (Mn) estimation by nonaqueous conductometric titration and thermogravimetry. All the polyureas were subjected to measure electrical conductivity at room temperature.

scholarly journals Direct Synthesis and Characterization of Photo-Crosslinkable Biodegradable PLA-PEG-PLA Ttiblock Copolymer with Methacrylates Functions by Green Montmorillonite Clay Catalyst

2020 ◽  
Vol 14 (4) ◽  
pp. 474-480
Author(s):  
Mohamed Benachour ◽  
◽  
Aslya El-Kebir ◽  
Amine Harrane ◽  
Rachid Meghabar ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Cationic Polymerization ◽  
Direct Synthesis ◽  
Average Molecular Weight ◽  
Montmorillonite Clay ◽  
Synthesis And Characterization ◽  
Molecular Weights ◽  
One Step ◽  
Clay Catalyst

Di-methacrylated PLA-PEG-PLA triblock copolymers of polylactide and polyethylene glycol were synthesized in one-step process by bulk cationic polymerization of lactide in the presence of PEG with different average molecular weights, using Maghnite-H+, an acidic montmorillonite clay, as a solid non-toxic catalyst. The obtained di-methacrylated copolymer was analyzed by 1H NMR and DSC. The effect of Maghnite-H+ proportions and PEG average molecular weight on the copolymerization and methacrylation yields and on average molecular weight of the resulting copolymers was studied.

Synthesis and characterization of a polyferrocenyldistannane

2014 ◽  
Vol 92 (6) ◽  
pp. 525-532 ◽  
Author(s):  
Jon Ward ◽  
Saif Al-Alul ◽  
Shane Harrypersad ◽  
Daniel A. Foucher
Keyword(s):  
Molecular Weight ◽  
Elemental Analysis ◽  
Ring Opening ◽  
Electronic Communication ◽  
Ring Opening Polymerization ◽  
Synthesis And Characterization ◽  
Vis Spectroscopy ◽  
Metal Catalyzed

The distannyl-bridged poly bis(dimethylstannyl)ferrocene, 5, was synthesized through either the metal-catalyzed intermolecular dehydrogenative condensation of the bis(dimethylstannyl)ferrocene, 6, or the ring-opening polymerization of the distannane-bridged [2]ferrocenophane, 7. Both polymerization strategies yielded compounds displaying NMR (1H, 13C, 119Sn) evidence for a distannane bridged polymer. A modest moderate molecular weight (GPC; Mw = 9.5 × 104 Da, PDI = 1.76) was found for polymer 5 prepared by dehydrogenative condensation. Polymer 5 displayed electronic communication (≈ 0.2 V) between neighbouring iron centers, similar to those reported for monobridged ferrocenyl stannane polymers. Polymer 5 was further characterized by UV–vis spectroscopy, elemental analysis, and modeled with the related distannyl-8 and tristannyl-9 bisferrocenes using DFT at the SDD level of theory.

CHARACTERIZATION OF SOME IRAQI ASPHALTS I. NUMBER AVERAGE MOLECULAR WEIGHT INVESTIGATION OF DORA AND QAIYARAH ASPHALTS

1986 ◽  
Vol 4 (3) ◽  
pp. 249-260 ◽  
Author(s):  
Mustafa M. F. Al-Jarrah ◽  
Hussain H. Al-Soufi ◽  
Rita L. Apikian ◽  
H. I. Al-Saleem ◽  
S. S. Naoom
Keyword(s):  
Molecular Weight ◽  
Average Molecular Weight ◽  
Number Average Molecular Weight

Preparation and characterization of novel soluble polyarylates derived from 9,9-bis[4-(4-chloroformylphenoxy)phenyl]xanthene with various bisphenols

2017 ◽  
Vol 30 (10) ◽  
pp. 1203-1209
Author(s):  
Yu-Ting Zhou ◽  
Shou-Ri Sheng ◽  
Chuan-Chao Tang ◽  
Cheng Song ◽  
Zhen-Zhong Huang ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Weight Loss ◽  
Room Temperature ◽  
Phase Transfer ◽  
Average Molecular Weight ◽  
Interfacial Polycondensation ◽  
Number Average Molecular Weight ◽  
Glass Transition Temperatures ◽  
Flexible Films

A series of new polyarylates bearing cardo xanthene groups were synthesized by phase-transfer-catalyzed interfacial polycondensation of 9,9-bis[4-(4-chloroformylphenoxy)phenyl]xanthene with various bisphenols containing the isopropylidene, hexafluoroisopropylidene, 1-phenylethylidene, diphenylmethane, cyclohexane, and xanthene structures. High-molecular-weight polyarylates with number-average molecular weight and polydispersity index in the range of 30,100–35,300 and 1.82–2.17, respectively, exhibited high glass transition temperatures ranged from 226°C to 261°C, and their 10% weight loss temperatures were in the range of 421–452°C with char yields above 45% at 700°C in nitrogen. All the polyarylates were amorphous and readily soluble in organic solvents such as dichloromethane, chloroform, tetrahydrofuran, meta-cresol, pyridine, N,N-dimethylformamide, N,N-dimethylacetamide, and 1-methyl-2-pyrrolidinone at room temperature and could be cast into tough, transparent, and flexible films with tensile strengths of 85.6–108.3 MPa, elongations at break of 2–3%, and tensile moduli of 7–9 GPa.

scholarly journals Synthesis and Characterizations of Biobased Copolymer Poly(ethylene-co-butylene 2,5-Furandicarboxylate)

2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Nam Vu Trung ◽  
Mai Ngoc Nguyen ◽  
Anh Nguyen Thi Ngoc ◽  
Ni Pham Thi ◽  
Tung Tran Quang ◽  
...  
Keyword(s):  
Molecular Weight ◽  
Ethylene Glycol ◽  
Structural Characterization ◽  
Average Molecular Weight ◽  
Step Process ◽  
Molar Ratios ◽  
Furandicarboxylic Acid ◽  
Poly Ethylene ◽  
Copolymer Poly

Homopolymers and copolymers derived from 2,5-furandicarboxylic acid have been extensively studied for their potential in the development of sustainable plastics. This research definitely spotlighted the synthesis of poly(ethylene-co-butylene 2,5-furandicarboxylate) copolymer via the two-step melting polycondensation with various ethylene glycol/1,4-butanediol molar ratios. The structural characterization of the obtained biobased copolymer was carried out by ATR-FTIR and 1H NMR. The average molecular weight of the obtained copolymer was determined by the intrinsic viscosity measurements. It was found that ethylene glycol was preferentially incorporated into the copolymer structures when the molecular weight of the products was not high enough (>18000). The decomposition of two types of monomer units of the obtained copolymer was proven through the degradation two-step process by TGA measurements.

scholarly journals Synthesis of co-poly(eugenol sulfonate)-DVB from eugenol as a major component of Syzygium aromaticum oils

2004 ◽  
Vol 2 (2) ◽  
pp. 53-57 ◽  
Author(s):  
DESI SUCI HANDAYANI ◽  
TRIANA KUSUMANINGSIH ◽  
MARIA YULI
Keyword(s):  
Molecular Weight ◽  
Melting Point ◽  
Average Molecular Weight ◽  
Nitrogen Atmosphere ◽  
Capillary Viscometer ◽  
Syzygium Aromaticum ◽  
Number Average Molecular Weight ◽  
Solid Matter ◽  
Concentrated Sulfuric Acid

Cationic co-polymerization between eugenol and divinylbenzene (DVB) (2%, 4%, 6%, 8%, 10% and 12%) with BF3O(C2H5)2 as a catalyst at room temperature without media under nitrogen atmosphere has been investigated. Co-poly (eugenol sulfonate)-DVB has been synthesized by sulfonation of co-poly(eugenol-DVB). In the sulfonation, concentrated sulfuric acid was used as the reagent and Ag2SO4 as a catalyst. Structure and characterization of co-poly (eugenol-DVB) and Co-poly(eugenol sulfonate)-DVB were analyzed by Infra Red (IR), Differential Thermal Analysis) DTA and UV-Vis. Measurement of the number-average molecular weight (Mn) of copolymer was used Ostwald capillary viscometer. The yields of co-polymerization of eugenol-DVB were solid matter and the highest result was found on a copolymer of 10% of DVB. Its melting point was 69.33oC. The increasing of mole of DVB increase the number-average molecular weight (Mn) of co-poly (eugenol sulfonate)-DVB. A copolymer of 12% of DVB gave the highest molecular weight, Mn = 2984 g/mole. Synthesized of co-poly (eugenol sulfonate)- DVB were solid matter too and the highest result was found on a copolymer of 12% of DVB. Its melting point was 95.5oC.

scholarly journals Synthesis and characterization of different soybean oil-based polyols with fatty alcohol and aromatic alcohol

e-Polymers ◽  
2021 ◽  
Vol 21 (1) ◽  
pp. 491-499
Author(s):  
Fukai Yang ◽  
Hao Yu ◽  
Yuyuan Deng ◽  
Xinyu Xu
Keyword(s):  
Molecular Weight ◽  
Soybean Oil ◽  
Retention Time ◽  
Ring Opening ◽  
Isoamyl Alcohol ◽  
Synthesis And Characterization ◽  
Intermolecular Force ◽  
H Nmr ◽  
Epoxy Groups

Abstract In this article, five kinds of soybean oil-based polyols (polyol-E, polyol-P, polyol-I, polyol-B, and polyol-M) were prepared by ring-opening the epoxy groups in epoxidized soybean oil (ESO) with ethyl alcohol, 1-pentanol, isoamyl alcohol, p-tert-butylphenol, and 4-methoxyphenol in the presence of tetrafluoroboric acid as the catalyst. The SOPs were characterized by FTIR, 1H NMR, GPC, viscosity, and hydroxyl numbers. Compared with ESO, the retention time of SOPs is shortened, indicating that the molecular weight of SOPs is increased. The structure of different monomers can significantly affect the hydroxyl numbers of SOPs. Due to the large steric hindrance of isoamyl alcohol, p-hydroxyanisole, and p-tert-butylphenol, SOPs prepared by these three monomers often undergo further dehydration to ether reactions, which consumes the hydroxyl of polyols, thus forming dimers and multimers; therefore, the hydroxyl numbers are much lower than polyol-E and polyol-P. The viscosity of polyol-E and polyol-P is much lower than that of polyol-I, polyol-B, and polyol-M. A longer distance between the molecules and the smaller intermolecular force makes the SOPs dehydrate to ether again. This generates dimer or polymers and makes the viscosity of these SOPs larger, and the molecular weight greatly increases.

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