• Title/Summary/Keyword: ester linkage

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Synthesis and Photocharacteristics of Bismaleimide Containing Ester Linkage (Ester Linkage를 함유한 Bismaleimide의 합성과 감광특성)

  • Kim, Sang-Min;Kim, Tae-Ho
    • Applied Chemistry for Engineering
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    • v.8 no.2
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    • pp.147-153
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    • 1997
  • Bismaleimides(BISMI) containing ester linkages were prepared by the chlorinated N-(p-carboxyphenyl)maleimide and N-(p-hydroxyphenyl)maleimide. The photosensitive properties of BISMI were investigated via changes of the irradiation time. Benzil dimethyl ketal was used as a photoinitiator. The effect of photoinitiator onto BISMI increase in average as increasing photoinitiator concentration and irradiation time. The yield of residual film and image pattern and resolution also measured and discussed.

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Determination of Mono- and Oligosaccharides Derivatized with p-Aminobenzoic Ethyl Ester by Reverse Phase HPLC

  • Kwon, Hyokjoon;Kim, Joon
    • Analytical Science and Technology
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    • v.8 no.4
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    • pp.859-864
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    • 1995
  • Mono- and oligosaccharides are derivatized with p-aminobenzoic ethyl ester (ABEE), strongly absorbs UV light at 254 nm, in the presence of sodium cyanoborohydride. C18-bonded silica column is used for the separation of sugar-ABEE derivatives in an isocratic mode. RP-HPLC conditions are optimized by using ternary mixture as mobile phase and $45^{\circ}C$ as a column temperature. Sugar-ABEE derivatives are separated well within a short run time (ca. 25 min) by reverse-phase partition chromatographic mode. The ($1{\rightarrow}6$) linkage type of dihexose-ABEE derivatives has shorter retention time than ($1{\rightarrow}4$)-linkage type. After acid hydrolysis of glycoproteins with 2M trifluoroacetic acid, monosaccharide composition and contents are determined. This procedure is very useful for the simultaneous analysis of neutral and amino sugars in a single chromatographic step using RP-HPLC without reacetylation of deacetylated amino sugars, which are produced by acid hydrolysis.

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Hydrolysis of the Ester Crosslinking on Cotton Fabric Treated with Polycarboxylic Acid(I) (polycarboxylic acid 처리면포의 Ester 가교결합의 가수분해 (I))

  • 강인숙;배현숙
    • Textile Coloration and Finishing
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    • v.15 no.4
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    • pp.24-31
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    • 2003
  • In this research, we applied FT-IR spectroscopy to study the hydrolysis of the ester-crosslinking formed by various polycarboxylic acids on the cotton fabric. We observed the following; (1) the ester-crosslinking is less durable to hydrolysis than ether-crosslinking under all conditions; (2) the ester-crosslinking formed by polycarboxylic acids having more than three carboxyl groups, such as butanetetracarboxylic acid (BTCA), are substantially more durable to hydrolysis than the acids having two or three carboxyl groups, such as maleic and citric acid; (3) alkaline conditions drastically accelerate the hydrolysis of both urea- and ester-crosslinking; and (4) the ester-crosslinking formed by poly(maleic acid) is more resistant to hydrolysis at alkaline conditions than BTCA. (5) polycarboxylic acid molecules were removed from the fabric at same rate as the hydrolysis of the ester linkage. FT-IR spectroscopy has proved to be a useful analytical technique for evaluating the hydrolysis of the crosslinked cotton fabric.

Hydrolysis of the Ester Crosslink on Cotton Fabric Treated with Combination of Poly(maleic acid) and Citric Acid (Poly(maleic acid)/Citric Acid 혼합 처리면포의 Ester 가교결합의 가수분해)

  • Kang In-sook;Bae Hyun-sook
    • Textile Coloration and Finishing
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    • v.17 no.3 s.82
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    • pp.16-25
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    • 2005
  • In this research, we investigated hydrolysis of the ester crosslinking on cotton fabric treated with polymer of maleic acid(PMA), citric acid(CA) and combination of polymer of maleic acid and citric acid using Fourier transform infrared spectroscophy. The rate of hydrolysis of the ester crosslinkage increased with pH regardless of the type of polycarboxylic acid used and even after hydrolysis for 256 hour in pH 13_4 solution, the treated fabric retained $10-20\%$ ester crosslinkage. The durability to alkaline hydrolysis of the ester crosslinkage formed by CA was lower than that of by PMA and combination of poly(maleic acid) and citric acid indicating that the ester formed by CA on the cotton fabric is more susceptible to hydrolysis than that formed by PMA and combination of PMA and CA. The total amount of ester and polycarboxylic acid molecules removed from fabric increased with increasing hydrolysis time but the rate of hydrolysis of ester linkage were higher than that of removal of polycarboxylic acid molecule from the fabric. The characteristic of hydrolysis of fabric treated with combination of PMA and CA was related with the mixing ratio of PMA and CA in treating fabric.

Cell Opening of High Resilience Polyurethane foam II. Structure Effect of Polyether Type Cell Opener (고탄성 폴리우레탄 발포체의 기포개방 II. 폴리에테르형 기포개방제의 구조 영향)

  • 송기천;이상목;이동호
    • Polymer(Korea)
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    • v.26 no.2
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    • pp.218-226
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    • 2002
  • For the preparation of high resilience polyurethane (PU) foams with polyether type cell openers which have different ethylene oxide (EO) content, molecular weight and chain structure, the influences of tell opener structure on the kinetics, rheology, structural stability, open cell content and mechanical properties of the obtained foam were investigated. It was observed that urea formation reaction was delayed with the increase of EO content and incorporation of ester linkage in cell opener molecule and was relatively independent on the molecular weight. With the rheological studies, the decreases of viscosity and storage modulus were confirmed for the increase of EO content and molecular weight, so that the resulted foam had low structural stability and high open cell content. The cell opener having ester linkage in molecule exhibited the lowest values of viscosity and storage modulus and the obtained foam has high open cell content. However, the structural stability increased due to the larger intermolecular interaction of ester linkage. The hardness, tensile strength, tear strength and elongation of foam were deteriorated with increase of EO content and molecular weight of tell opener. On the other hand, the cell opener having ester linkage in molecule improved the values of tensile strength, tear strength and elongation.

Synthesis and Properties of Liquid Crystalline Copolymers with Ether-ether-ester Linkage in Main Chain (주사슬에 ether-ether-ester 결합을 갖는 액정공중합체의 합성 및 성질)

  • Bang, Moon-Soo
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.11 no.4
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    • pp.1367-1372
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    • 2010
  • Copoly(ether-ether-ester)s having flexible side chain were synthesized by polycondensation. Intrinsic viscosities of polymers were between 0.42 and 0.78dl/g in tetrachloroethane. The polymer structures were investigated by $^1H$-NMR and FT-IR, and thermal and liquid crystalline properties of polymers were measured by DSC, TGA, POM and XRD. As results of investigations, synthetic copolymers exhibited lower melting temperature than homopolymers. When the biphenylene units contents in copolymer were more than 60 mol %, nematic mesophase was observed, and the mesophase of synthetic polymers was dependent upon biphenylene content.

Characterization of Hyaluronic Acid Membrane Containing Lactic Acid (젖산이 결합된 히아루론산 막의 특성)

  • Cheong Seong Ihl;Kwon Ji Young
    • Membrane Journal
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    • v.15 no.1
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    • pp.8-14
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    • 2005
  • The hyaluronic acid (HA) with excellent biocompatibility can be combined with the monomer polylactide with good biodegradability to produce biocompatible materials which can control the period of degradation in a human body. By freeze drying method, HA and the lactic acid, monomer of polylactide, or lactide, the ester dimer of polylactide, were crosslinked with crosslinking agent, l-ethyl-3-(3-dimethyl aminopropyl) carbodiimide. The analysis of infrared spectroscopy showed that the ester linkage was formed and the analysis of nuclear magnetic resonance (NMR) spectroscopy showed that the ester linkage was due to the reaction of lactic acid and HA. The conversion (6∼32%) and degree of crosslinking (4∼19%) increased but the selectivity was almost constant at 62% as the mole ratio of LA to HA increased from 1 to 10 in the crosslinking reaction. The brittleness became more pronounced and the rate of degradation became faster with more addition of lactic acid resulting from the higher ratio of LA to HA, and the swelling ratio was in the range of 500 to 2000%.

Development of New Soft Contact Lens Materials Using Ester-Monomers of Itaconic Acid from Aspergillus itaconicus (Aspergillus itaconicus 유래 itaconic acid의 ester-monomer를 이용한 새로운 soft contact lens 소재 개발)

  • You, Young-Hyun;Nam, Joo-Hyeung;Kim, Bieong-Kil;Kim, Soon-Bok;Moon, Ik-Jae;Kim, Jong-Pil;Seu, Young-Bae
    • Journal of Life Science
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    • v.19 no.4
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    • pp.538-542
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    • 2009
  • In this study, we confirmed water content and oxygen permeability of new polymeric materials synthesized from itaconic acid used for soft contact lenses. In this study, we polymerized materials for soft contact lenses using HEMA (2-hydroxyethyl methacrylate), the based-monomer of soft contact lenses, EGDMA (ethylene glycol dimethacrylate) as a cross linkage agent, and the new additives mono-ester or di-ester derived from itaconic acid commercially produced by the fermentation of A. itaconicus. New polymer materials for contact lenses were synthesized with the mixture of HEMA and mono- or di-ester at different ratios and water content and oxygen permeability (Dk) was analyzed. In polymerizing HEMA and mono-ester (15%), the water content and oxygen permeability of contact lenses were found to be of good value at 57.7% and 28.6 Dk respectively. The mixture of HEMA and mono-ester is more excellent than HEMA/di-ester in regards to water content and oxygen permeability. The water content and oxygen permeability of soft contact lenses made by new polymeric materials were highly represented.

Conformational Study of Liquid Crystalline Polymer: Theoretical Studies

  • Lee, Mi-Jung;Kim, Dong-Hee
    • Bulletin of the Korean Chemical Society
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    • v.27 no.1
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    • pp.39-43
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    • 2006
  • The relaxed torsional potential of a liquid crystalline polymer containing an ester functional group in a mesogenic unit (hereafter 12-4 oligomer) has been calculated with the ab initio self-consistent-field using 6-31G$^*$ basis set. GIAO^{13}C NMR chemical shifts also have been calculated at the B3LYP/6-31G$^*$ level of theory for each conformational structure obtained from torsional potential calculation. The results show that the phenyl ring-ester linkages are coplanar with the dihedral angle of about 0$^{\circ}$ and the ring-ring linkages in the biphenyl groups are tilted with the dihedral angle of around 43-44$^{\circ}$ in the lowest energy conformer. The biphenyl ring has a comparatively lower energy barrier of internal rotation potential in the ring-ring than that of phenyl ring-ester. The ^{13}C chemical shifts of carbonyl carbons were found to move to upfield due to $\pi$ -conjugation with phenyl ring and slightly affected about 0.5 ppm by dihedral angle of the ring-ring linkage.

Structural Characterization of Purified Fucoidan from Laminaria religiosa, Sporophylls of Undaria pinnatifida, Hizikia fusiforme and Sagassum fulvellum in Korea (국내산 다시마, 미역포자엽, 톳, 모자반 정제 fucoidan의 구성당 결합 특성)

  • Koo Jae-Geun
    • Korean Journal of Fisheries and Aquatic Sciences
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    • v.30 no.1
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    • pp.128-131
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    • 1997
  • Primary structure of purified fucoidans was analysed by methanolysis, methylation and HT-IR measurement. Basic linkage in the fucoidans of Laminaria religiosa, sporophylls of Undaria pinnatifida, Hizikia fusiforme and Sargassum fuivellum from Korea was $(1\rightarrow3)$ linkage of fucose, but a considerable amount of $(1\rightarrow3)$ linked galactose was also found in case of the purified fucoidan from sporophylls of U. pinnatifida. Ester sulfate was substituted mainly to C-4 position of fucose and galactose.

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