Добірка наукової літератури з теми "Ether linkage"
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Статті в журналах з теми "Ether linkage"
Andersen, F. Alan. "Special Report: Reproductive and Developmental Toxicity of Ethylene Glycol and Its Ethers." International Journal of Toxicology 18, no. 2_suppl (March 1999): 53–67. http://dx.doi.org/10.1177/109158189901800208.
Повний текст джерелаZhou, Jinghui, Xinjin Sui, and Haiqiang Shi. "Study on the structural change of lignin during auto-catalyzed ethanol-water pulping of aspen by 1H-NMR." BioResources 4, no. 3 (June 1, 2009): 979–85. http://dx.doi.org/10.15376/biores.4.3.979-985.
Повний текст джерелаDuvva, Naresh, A. R. Ramya, Govind Reddy, and L. Giribabu. "Intramolecular electron transfer in porphyrin-anthraquinone donor–acceptor systems with varying molecular bridges." Journal of Porphyrins and Phthalocyanines 23, no. 06 (May 28, 2019): 628–38. http://dx.doi.org/10.1142/s1088424619500287.
Повний текст джерелаBang, Moon-Soo. "Synthesis and Properties of Liquid Crystalline Copolymers with Ether-ether-ester Linkage in Main Chain." Journal of the Korea Academia-Industrial cooperation Society 11, no. 4 (April 30, 2010): 1367–72. http://dx.doi.org/10.5762/kais.2010.11.4.1367.
Повний текст джерелаZhao, Rui, Pan Shi, Junyou Chen, Shuaishuai Sun, Jingnan Chen, Jibin Cui, Fangming Wu, et al. "Chemical synthesis and biological activity of peptides incorporating an ether bridge as a surrogate for a disulfide bond." Chemical Science 11, no. 30 (2020): 7927–32. http://dx.doi.org/10.1039/d0sc02374d.
Повний текст джерелаNi, Zhi-Yu, Yi-Bing Wu, Mei Dong, Man-Li Zhang, Yu-Fang Wang, Françoise Sauriol, Chang-Hong Huo, et al. "Diabietane Ether, a New Dimeric Abietane with an Ether Linkage from Taxus cuspidata Needles." Zeitschrift für Naturforschung B 66, no. 10 (October 1, 2011): 1083–86. http://dx.doi.org/10.1515/znb-2011-1015.
Повний текст джерелаKikuchi, Shuhei, Yugo Iwasaki, Mina Yoshioka, Kodai Hino, Shin-ya Morita, Ryu Tada, Yasuhiro Uchimura, et al. "Solitary and Synergistic Effects of Different Hydrophilic and Hydrophobic Phospholipid Moieties on Rat Behaviors." Pharmaceutics 16, no. 6 (June 4, 2024): 762. http://dx.doi.org/10.3390/pharmaceutics16060762.
Повний текст джерелаLundquist, Knut, Vratislav Langer, and Jim Parkås. "The structure and conformation of lignin as judged by X-ray crystallographic investigations of lignin model compounds: Arylglycerol beta-syringyl ethers." BioResources 4, no. 2 (March 5, 2009): 529–36. http://dx.doi.org/10.15376/biores.4.2.529-536.
Повний текст джерелаXie, Yimin, Xudong Chen, Kai Zhang, Sheng Cui, and Gongxia Zhang. "Elucidation of lignin and polysaccharide linkages in wheat straw by 2H/13C isotopic tracer." BioResources 18, no. 1 (November 17, 2022): 550–69. http://dx.doi.org/10.15376/biores.18.1.550-569.
Повний текст джерелаGrainger, James, V. Vikram Reddy, and Donald G. Patterson. "Pentachlorodibenzo-p-dioxin Isomer Differentiation by Capillary Gas Chromatography Fourier Transform Infrared Spectroscopy." Applied Spectroscopy 42, no. 5 (July 1988): 800–806. http://dx.doi.org/10.1366/0003702884429166.
Повний текст джерелаДисертації з теми "Ether linkage"
Badami, Anand Shreyans. "Morphological and Structure-Property Analyses of Poly(arylene ether sulfone)-Based Random and Multiblock Copolymers for Fuel Cells." Diss., Virginia Tech, 2007. http://hdl.handle.net/10919/29469.
Повний текст джерелаPh. D.
Azevedo, Rafael Raphaela. "Development of catalysts for the valorization of lignin : hydrodeoxygenation of dimeric aryl ethers." Electronic Thesis or Diss., Université de Lille (2022-....), 2022. http://www.theses.fr/2022ULILR041.
Повний текст джерелаThe present thesis aims at studying the role of the support and metal particle size on the hydrodeoxygenation reactions (HDO) of benzyl phenyl ether (BPE), phenethoxybenzene (PEB), and diphenyl ether (DPE) chosen as model molecules representative of the main ether linkages present in the lignocellulosic biomass. The reactions were carried out in liquid phase at 230 °C and 18 bar of H2. Pd supported on different oxides (SiO2, TiO2, Nb2O5, Al2O3, ZrO2, and HZSM5) were synthesized by incipient wetness impregnation and deposition of metal particles prepared by colloidal method. The acidic sites of the support promote the cracking of the C-O ether bond of BPE, but for PEB and DPE, this effect is less pronounced due to the higher energy required to break these linkages. The hydrogenolysis of the C-O ether bond takes place on the metallic Pd particles, producing the respective arenes. However, the Pd particle size can directly affect the product distribution after C-O cleavage. Due to the larger Pd particle size, impregnated catalysts favor the hydrogenolysis and exhibit a higher selectivity to alkylated products, whereas a smaller Pd particle size, obtained for catalysts prepared by the colloidal route, increases the selectivity to deoxygenated products. Over these catalysts, the formation of alkylated products is suppressed, but the hydrogenation of BPE, PEB, and DPE aromatic rings occurs in parallel to hydrogenolysis also promoted by Pd particles. The performance of Ru-based catalysts was also evaluated in the same reaction conditions. In the presence of Ru, alkylated products are produced even in the absence of acidic sites
Kaurich, Kevin Joseph. "Segmented Aromatic Polymers Containing Thermally Reversible Linkages." Diss., Virginia Tech, 2019. http://hdl.handle.net/10919/87533.
Повний текст джерелаPHD
This dissertation describes a new synthetic approach to polymeric materials that can heal themselves (for example, repair small cracks that may have formed due to stress or aging) simply by heating the damaged area. Our approach uses a thermally reversible chemical reaction (called the Diels-Alder reaction) to connect several shorter polymer segments into longer chains. Upon heating, the segments can come apart, diffuse into and through the damaged area, and then rejoin. The first chapter is a review of background in the published literature as well as previous not-yet-published work in our laboratory. The second chapter describes the creation of new building-block molecules (monomers) that will help control the temperature range necessary to induce self-healing after incorporation into the polymer segments. The third chapter details the process of forming the segments, the incorporation of self-healing functionalities on the ends of the segments, the joining of the segments into longer polymeric chains, and the testing of all of the physical properties of these new materials, including their self-healing capabilities. The fourth chapter represents a preliminary study of a new method of preparing ion-containing polymers. The latter materials have potential use in various membrane technologies including fuel cell devices for the harnessing of renewable energy.
Idage, S. B. "Synthesis and characterization of polymers containing i) arylene sulfone ether and ii) aromatic azomethine linkages." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 1991. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/3042.
Повний текст джерелаLuo, Shih-Ci, and 羅仕頎. "Synthesis and Characterization of Triazole Metal Complexes Containing Ether Linkage." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/hgk35e.
Повний текст джерелаCHIU, PEI-FANG, and 邱沛芳. "Design and Synthesis a Water-soluble Group for Ether-linkage of 10-Hydroxycamptothecin Prodrug." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/686w4t.
Повний текст джерела嘉南藥理大學
藥學系
105
Camptothecin has good anti-cancer activity, and current clinical use of two derivatives are Topotecan and Irinotecan which improve poor water solubility of Camptothecin by chemical modification. However, the lack of drugs specificity of tumor will cause severe side effects. Therefore, our laboratory designed and synthesized two glucuronide prodrugs of Camptothecin (9-ACG and 10-HCG) which will mainly be activated at tumor site expressing large number of β-glucuronidase. According to previous studies, 9-ACG and 10-HCG was 1800 and 20 times soluble than 10-HCG, respectively; 9-ACG and 10-HCG was 30-fold and 10-fold less toxic than the parent drug to cells, respectively; Enzyme kinetic studies showed that β-glucuronidase exhibited 520 times higher catalytic efficiency for 10-HCG than for 9-ACG, and molecular modeling studies predicted that 10-HCG would have a higher binding affinity to enzyme than 9-ACG. In this study, we design and synthesize the target compound 10-HCPG by creating N-methyl piperazine on the benzyl group of 10-HCG, expect for good water solubility, stable in blood, low cytotoxicity, good affinity with β-glucuronidase and specific to tumor cells.
Huang, Yi-Hsiung, and 黃益雄. "Design,synthesis and investigation on the blue phase liquid crystal materials with ether linkage." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/93150914622866018677.
Повний текст джерела大同大學
化學工程學系(所)
98
ABSTRACT The primary research work of this study is an attempt to correlate the structure-property relationship of the formation of blue phases in chiral liquid crystals in terms of variation of the structure of the rigid cord, achiral alkyl chain length (m) and chiral alkyl chain length (n) possessing ether linkage attached to the chiral tail in the chiral liquid crystal materials. Thus, the optically active alcohols, 2-octanol, 1-butyloxy-2-propanol, 1-pentyloxy-2-propanol, 1-hexyloxy-2-propanol, were designed and synthesized by reacting (S)-propylene oxide with alkyl alcohols under basic condition. In consequence, five novel homologous series of chiral materials, (R)-6-(1-methylheptyloxy)naphth-2-yl 4’-octyloxybenzoate, I(m), (R)-6-(1-butyloxy-2-propyl)naphth-2-yl 4-octyloxybenzoate, II(m), (R)-6-(1-pentyloxy-2-propyl)naphth-2-yl 4-octyloxybenzoate, III(m), (R)-6-(1-hexyloxy-2-propyl)naphth-2-yl 4-octyloxybenzoate, IV(m), (R)-4-(1-butyloxy-2-propyl)biphenyl 4-octyloxybenzoate, V(m), derived from these alcohols were synthesized for the investigation of the effect of the aliphatic alkyl chain length (m), ether linking group, chiral tail alkyl chain length (n) and rigid core structures on the mesomorphic and electro-optical properties. The mesomorphic phases and their corresponding transition temperatures were primarily characterized by the microscopic textures and DSC thermograms, and the ferroelectric phases were further identified by the measurements of electric switching behavior and dielectric constant ε'. The results of compounds I(m) composed of the rigid core structure of PhCOONa and chiral group of optical activity 2-octanol, showed that compound I(m=6) exhibits the mesophases sequence of BPIII-BPII-N*, compound I(m=7) exhibits the mesophases sequence of BPII-BPI-N* and compounds I(m=8,9) exhibits the mesophases sequence of BPII-BPI-N*-TGBA*-SmA*. With the exception of I(m=8) that exists the widest temperature range of enantiotropic BPII and BPI phases, the rest of compounds in series of I(m) possess BPII and BPI phases are monotropic. Compounds I(m) display frustrated phases demonstrated that these compounds possess high chirality. The results of compound II(m=6, n=4), composed of the same rigid core structure as compound I(m) but differed in the chiral group where an additional ether linkage is introduced, shows the mesophases sequence of BPII-BPI-N*, compounds II(m=7, 8, 9, n=4) exhibit the mesophases sequence of BPII-BPI-N*-TGBA* and compound II(m=8, n=4) displayed an additional SmA* phase. All compounds posses enantiotropic BPII and BPI phases and the thermal stability of BPI and TGBA* phases increase from compounds at m=7 to m=8 and m=9. When extending the alkyl length (n) of chiral tail, the thermal stability of TGBA* phase decreases and when n=5 and 6, the BPI is suppressed. The widest temperature range of frustrated (BP and TGBA*) phases for these compounds appeared at n=4. The results of compounds V(m=7-9, n=4), composed of the same chiral group but differed in the rigid core structure (PhCOOPhPh) as compounds II(m), show the mesophases sequence of BPII-BPI-N*-SmC*, compound V(m=9, n=4) exhibit an additional BPIII phase. The thermal stability of BPII and BPI phases obtained from compounds V(m) are decreased and the TGBA* phase is suppressed as compared to that of compounds II(m). The physical properties of the chiral materials in ferroelectric SmC* phases were measured. The maximum magnitudes of spontaneous polarization measured for the materials in the SmC* phase are in the range of 21.7 to 28.5 (nC/cm2). These results also show that the maximum Ps values have no significant correlation to the change of achiral alkyl chain length (m). In conclusion, the chiral materials composed of the rigid core structure of PhCOONa and the chiral group of an additional ether linkage at terminal tail of the molecules, have higher thermal stability of frustrated (BP and TGBA*) phases. All series of compounds display that achiral alkyl chain length (m) of the molecules have no correlation to the thermal stability of the frustrated phases, nevertheless, chiral alkyl chain length (n) of molecules show an increasing in thermal stability of frustrated phases in decreasing n. Among all compounds, compound II(m=7, n=4) has the widest temperature range of enantiotropic blue phases (cal. 12.5℃). Keywords: Chiral material, Blue phase, frustrated phases, electro-optical property, switching behavior, dielectric constant ε’
Chen, Pei-Min, and 陳佩敏. "Tandem Cyclization of Enynes Containing an Ether Linkage and a Cyclopropyl Group via Ruthenium Metal Complex." Thesis, 2014. http://ndltd.ncl.edu.tw/handle/72759808192027849035.
Повний текст джерела國立臺灣大學
化學研究所
102
We study chemical reactions of [Ru]Cl ([Ru] = Cp(PPh3)2Ru) with three 1,8-enyne compounds containing cyclopropyl group (1, 7 and 11) in which the triple bond is associated with propargylic alcohol and the ole&;#64257;nic group has various substituted methyl groups. The reaction of [Ru]Cl and 1, containing one methyl group added to the internal carbon of the allyl group, affords the vinylidene complex 2 with a newly formed seven-membered ring. Furthermore, tandem cyclization reaction of 1 in MeOH/CHCl3 catalyzed by [Ru]NCCH3+PF6- at 60 oC leads to the product 6 with spiro-cyclopropyl ring, formed possibly via sequential allenylidene vinylidene cyclization followed by a nucleophilic addition of alkoxide. In CHCl3, the catalytic reaction by [Ru]NCCH3+ PF6- gives the isolable organic cyclization intermediate enyne 5. Treatment of the propargylic alcohol 7 containing two terminal methyl groups at the O-allylic group, with [Ru]Cl yields a mixture of two diastereomers of the vinylidene complex 8 containing a newly formed six-membered ring in a ratio of ca. 10:1. Among diastereoisomers only the anti-isomer is isolated for complex 8. The cyclization reaction is proposed to proceed via the formation of a six-membered ring boat-like transition state with bulkiest group in the pseudo-equatorial position to reduce the 1,3-diaxial interactions. The catalytic reaction by [Ru]NCCH3+PF6- in CHCl3 at 60 oC affords anti-9 and syn-9 in a ratio of 3:1. The thermal energy increases amount of product syn-9. The subsequent cyclization carried out in a cosolvent of ROH/CHCl3 at 60 oC affords bicyclic product 10. In the reaction of [Ru]Cl with 11, containing no methyl group, no C&;#8722;C bond formation is observed. The reaction of 11with [Ru]Cl in the presence of NH4PF6 in CH2Cl2 affords a mixture of the allenylidene complex 12 and phosphonium acetylide 13. Interestingly, thermal treatment of 11 leads to a ring expansion of the cyclopropyl group, giving the vinylidene complex 16 with a five-membered ring. This ring expansion proceeds by C-C bond formation between Cβ of the cumulative double bond and a methylene group of the cyclopropyl ring. Reaction of 1,3-diol 18 with [Ru]Cl in CH2Cl2 yields a mixture of the alkoxy carbene 17 and 19 in a ratio of 1:2. The spontaneous dehydration of 19 to 17 by elevating temperature is failed. Fortunately, complex 17 could be the only product when the reaction is carried out in MeOH. Overall, tandem cyclizations of two 1,8-enynes with methyl-substituents have been achieved. Ring-expansion of a cyclopropyl group in a 1,8-enyne with no methyl-substituent is also accomplished.
Leu, Tsu-Shang, and 呂祖尚. "Novel High Performance Polymers Containing Naphthalene Pendant Group and Flexible Ether Linkages." Thesis, 1999. http://ndltd.ncl.edu.tw/handle/97042813376615081494.
Повний текст джерела國立成功大學
化學工程學系
87
Abstract High performance resins are very useful in highly demanding environments to provide special properties, such as thermal stability, good chemical resistance, high dimensional stability, low water absorption and high mechanical strength. Unfortunately, most high performance polymers suffer from their poor solubility in organic solvent, extremely high melting points, and high melt viscosity for fabrication. The processability of high performance polymers can be improved by the reduction of their molecular weight. However, this approach results in a significant decrease of their final thermal and physical properties. Therefore, one successful approach to increase solubility and processability of polymers without sacrificing their thermal and physical properties is by the modification of polymer structure. In this thesis, we plan to combine the special features of naphthalene structure (rigid, low moisture absorption and low coefficient of thermal expansion) with bismaleimides and polyimides (high crosslink density, good thermal and electrical properties) in order to produce a new high performance material. The goal of this study is to synthesize a new epoxy, bismaleimide and diamine monomers. A series of novel high performance polymers containing naphthalene pendant group and flexible ether linkages have been prepared which include epoxy resins, polyaspartimides, polyaminobismaleimides and polyimides. The primary aim of this work was to illustrate the effect of function groups on the properties of polymers, such as solubility, bulk density, thermal properties, moisture absorption, dynamic mechanical properties, dielectric constant, coefficient of thermal expansion and mechanical properties. Novel bismaleimide (BMI) and epoxy resin with naphthalene side group were synthesized from the intermediates, bis(4-amino-3,5-dimethylphenyl)naphthylmethane (BADN) and bis(4-hydroxy-3,5-dimethylphenyl)naphthylmethane (BHDN), which were obtained from the reactions between 1-naphthaldehyde and 2,6-dimethylaniline or 2,6-dimethylphenol, respectively. The monomers were characterized by fourier transform infrared spectroscopy, elemental analysis, mass spectrometry, nuclear magnetic resonance spectrometry and potentiometery. Their corresponding bismaleimide bis(4-maleimido-3,5-dimethylphenyl)naphthylmethane (BMDN) and the diglycidyl ether of BHDN (DGEBN) were cured with 4,4''-diaminodiphenyl methane (DDM) at various mole ratio and their curing behaviors investigated by differential scanning calorimetry (DSC) and FTIR. Thermogravimetric analyses (TGA) indicated that the cured systems of bismaleimide and epoxy resins were stable up to 416-424℃ and 377-395℃, respectively, in nitrogen atmosphere, and the former afforded a relatively higher char yield than the latter. In addition, the cured bismaleimide possessed better Tg, moisture resistance, lower coefficient of thermal expansion and dielectric constant than that of the epoxy system. A bismaleimide, bis(4-maleimidophenoxy-3,5-dimethylphenyl)naphth- ylmethane (BMPDN), containing a pendant naphthalene and aryl ether linkage was synthesized from bis(4-hydroxy-3,5-dimethylphenyl)-naphthylmethane (BHDN) through a diamine, [bis(4-aminophenoxy-3,5-dimethylphenyl)naphthylmethane (BAPDN)], and maleic anhydride by the usual two step procedure that included ring opening addition to give bismaleamic acid, followed by cyclodehydration to bismaleimide. A series of polyaspartimides, polyaminobismaleimides were prepared by the polyaddition of this bismaleimide with diamine (DDM) at various mole ratio via a Michael-type addition in the melt. The new BMI was found to possess the processability and solubility. In addition, it also exhibited increasing thermal stability and better physical properties with decreasing DDM concentration. A series of novel polyimides containing pendant naphthalene and flexible ether moieties were prepared from various diamines [including bis(4-amino-3,5-dimethylphenyl)naphthylmethane, bis(4-aminophenoxy-3,5-dimethylphenyl)naphthylmethane and bis(4-aminophenoxy-3,5-dimethylphenyl)methane] with various aromatic tetracarboxylic dianhydrides via a two-step and one-step methods. All polyimides, except those without naphthalene pendant group, were readily soluble in common organic solvent, such as chloroform. Differential scanning calorimetry (DSC) revealed that the naphthalene bearing diamine monomers had a low entropy, and formed amorphous polyimides. They retained high moduli even at high temperatures by dynamic mechanical analysis (DMA), and had their coefficients of thermal expansion (CTEs) in the range of 46.86-67.14ppm by thermomechanical analysis (TMA). The glass transition temperature of polyimides were found to be 268-294℃, 298-326℃ and 270-315℃ respectively by DSC, DMA, and TMA. Thermogravimetric analyses indicated that they were fairly stable up to 489-571℃ (10wt% loss in N2). In addition, they had a tensile strength in the range of 56-97Mpa, and an elongation to break of around 3%. These polyimide films have dielectric constants ranging from 2.71 to 3.28 with moisture absorptions of less than 0.98%.
Huang, Perng-Chih, and 黃鵬誌. "Synthesis and Properties of Aromatic Polyamides and Polyimides Bearing Ether and Sulfone Linkages in the Main Chain." Thesis, 1997. http://ndltd.ncl.edu.tw/handle/48753303488700673361.
Повний текст джерелаКниги з теми "Ether linkage"
Patai, Saul. Chemistry of the Ether Linkage. Wiley & Sons, Limited, John, 2010.
Знайти повний текст джерелаPatai, Saul. Chemistry of the Ether Linkage, Part 1. Wiley & Sons, Incorporated, John, 2018.
Знайти повний текст джерелаCook, Diana Lynn. Synthesis of polybenzimidazoles containing arylene sulfone and ether linkages. 1993.
Знайти повний текст джерелаЧастини книг з теми "Ether linkage"
Smith, Dennis W., Junmin Ji, Sridevi Narayan-Sarathy, Robert H. Neilson, and David A. Babb. "Fluorosilicones Containing the Perfluorocyclobutane Aromatic Ether Linkage." In ACS Symposium Series, 308–21. Washington, DC: American Chemical Society, 2000. http://dx.doi.org/10.1021/bk-2000-0729.ch020.
Повний текст джерелаHagen, A. P. "By Cleavage of Ether Linkages." In Inorganic Reactions and Methods, 209–10. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470145197.ch167.
Повний текст джерелаSkovby, Michael H. B., Claus A. Heilmann, and Jørgen Kops. "All-Aromatic Liquid-Crystalline Polyesters of Phenylhydroquinone with Ether and Ketone Linkages." In ACS Symposium Series, 46–61. Washington, DC: American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0435.ch004.
Повний текст джерелаSubramaniam, Ram, and D. Allen Butterfield. "Structure-Activity Correlation of Subtilisin Immobilized on Modified Poly (Ether) Sulfone Membrane by Covalent and Non-Covalent Linkages." In Biofunctional Membranes, 201–8. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4757-2521-6_14.
Повний текст джерелаCalvert, Jack, Abdelwahid Mellouki, John Orlando, Michael Pilling, and Timothy Wallington. "Rate Coefficients and Mechanisms for the Atmospheric Oxidation of the Ethers." In Mechanisms of Atmospheric Oxidation of the Oxygenates. Oxford University Press, 2011. http://dx.doi.org/10.1093/oso/9780199767076.003.0006.
Повний текст джерелаBronfman, Alejandra. "Receivers." In Isles of Noise. University of North Carolina Press, 2016. http://dx.doi.org/10.5149/northcarolina/9781469628691.003.0003.
Повний текст джерелаHan, Chang Dae. "Rheology of Thermoplastic Polyurethanes." In Rheology and Processing of Polymeric Materials: Volume 1: Polymer Rheology. Oxford University Press, 2007. http://dx.doi.org/10.1093/oso/9780195187823.003.0016.
Повний текст джерелаТези доповідей конференцій з теми "Ether linkage"
Gershenson, J. K., B. D. Solomon, D. R. Shonnard, D. W. Watkins, and J. W. Sutherland. "Production Decision Making in the Face of Uncertainty About Air Toxics Regulation and Global Climate Change Policy." In ASME 2001 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2001. http://dx.doi.org/10.1115/imece2001/ts-23414.
Повний текст джерелаQi, Yinghua, Jianfu Ding, Michael Day, Jia Jiang, and Claire L. Callender. "Design, synthesis, and properties of cross-linkable fluorinated poly(arylene ether ketone)s." In Photonics North, edited by John C. Armitage, Simon Fafard, Roger A. Lessard, and George A. Lampropoulos. SPIE, 2004. http://dx.doi.org/10.1117/12.567379.
Повний текст джерела