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Journal articles on the topic 'Decene-1'

Author: Grafiati

Published: 5 June 2025

Last updated: 16 July 2025

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1

Jalili, Amir Hossein, and Mitra Sina. "Isobaric Vapor−Liquid Equilibria of Hexane + 1-Decene and Octane + 1-Decene Mixtures." Journal of Chemical & Engineering Data 53, no. 2 (2008): 398–402. http://dx.doi.org/10.1021/je700445y.

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2

Aimar, Mario L., and Rita H. de Rossi. "Kinetics of the Isomerization of 1-Decene to cis- and trans-2-Decene." Journal of Organic Chemistry 60, no. 13 (1995): 4255–57. http://dx.doi.org/10.1021/jo00118a048.

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3

Seidova, Kh., Zh. Akhmedli та T. Budagova. "IONIC LIQUIDS IN THE FIELD OF OLIGOMERIZATION OF α-OLEFINS". Sciences of Europe, № 143 (26 червня 2024): 18–19. https://doi.org/10.5281/zenodo.12540697.

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The article describes the results of a study of the properties of oils obtained by oligomerization of hexene-1 and decene-1 in the presence of ionic-liquid catalytic systems (ILCS). Various indicators of the synthesized oligoalkylnaphthenic oil fractions were determined (density, melting point, molecular weight, molecular weight distribution, ignition and freezing temperatures, viscosity index, etc.).

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4

Hanifpour, Ahad, Naeimeh Bahri‐Laleh, and Mehdi Nekoomanesh‐Haghighi. "Single‐phase photo‐cross‐linkable adhesive synthesized from methacrylic acid‐grafted 1‐decene/9‐decene‐1‐ol cooligomer." Journal of Applied Polymer Science 138, no. 2 (2020): 49654. http://dx.doi.org/10.1002/app.49654.

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5

Varyani, Manish, Indrajit K. Ghosh, and Suman L. Jain. "Copper ingrained poly(ethylene)glycols as cost effective and reusable media for selective 1-decene/n-decane separation." RSC Advances 5, no. 94 (2015): 77037–41. http://dx.doi.org/10.1039/c5ra11370a.

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6

Huxoll, Fabian, Stefan Schlüter, Robert Budde, et al. "Phase Equilibria for the Hydroaminomethylation of 1-Decene." Journal of Chemical & Engineering Data 66, no. 12 (2021): 4484–95. http://dx.doi.org/10.1021/acs.jced.1c00561.

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7

Zanini, Stefano, Elisa C. Dell'Orto, and Claudia Riccardi. "Characterization of plasma deposited poly(heptadecafluoro-1-decene)." Surface and Coatings Technology 307 (December 2016): 9–16. http://dx.doi.org/10.1016/j.surfcoat.2016.08.064.

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8

Xu, Jun-Ting, Liang Xue, and Zhi-Qiang Fan. "Nonisothermal crystallization of metallocene propylene-decene-1 copolymers." Journal of Applied Polymer Science 93, no. 4 (2004): 1724–30. http://dx.doi.org/10.1002/app.20643.

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9

Engel, Rebecca V., Raiedhah Alsaiari, Ewa Nowicka, et al. "Oxidative Carboxylation of 1-Decene to 1,2-Decylene Carbonate." Topics in Catalysis 61, no. 5-6 (2018): 509–18. http://dx.doi.org/10.1007/s11244-018-0900-y.

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10

Pe�a, B., J. A. Delgado, E. P�rez, and A. Bello. "Crystallinity and thermal properties of ethylene-1-decene copolymers." Polymer Bulletin 31, no. 1 (1993): 89–95. http://dx.doi.org/10.1007/bf00298769.

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11

Divekar, S. S., B. M. Bhanage, R. M. Deshpande, R. V. Gholap, and R. V. Chaudhari. "Selectivity in hydroformylation of 1-decene by homogeneous catalysis." Journal of Molecular Catalysis 91, no. 1 (1994): L1—L6. http://dx.doi.org/10.1016/0304-5102(94)00045-x.

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12

Ismayilova, Sabira Sabir, and Sabir Qarsh Amirov. "Dearomatization of the Kerosene Fraction: Kinetic Studies." Catalysis Research 2, no. 2 (2022): 1. http://dx.doi.org/10.21926/cr.2202017.

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The kinetics of dearomatization of a kerosene fraction processed using a zeolite catalyst (0.9 HZSM-5) at different temperatures (160-200°C), the molar ratio between the aromatic hydrocarbons present in the kerosene fraction and n-decene (1:(0.5-4)), and the reaction time (1-3 h) were studied. Based on the obtained data, a kinetic model for kerosene dearomatization is proposed. It is assumed that the single-center Riedel mechanism is followed. The stage associated with the interaction between n-decene adsorbed on the surface of the catalyst containing aromatic compounds and n-decene present in the volume is identified as the limiting sage of the dearomatization process.

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13

Pierro, Ivana, Giuseppe Leone, Giorgia Zanchin, Maurizio Canetti, Giovanni Ricci, and Fabio Bertini. "Polyolefin thermoplastic elastomers from 1-octene copolymerization with 1-decene and cyclopentene." European Polymer Journal 93 (August 2017): 200–211. http://dx.doi.org/10.1016/j.eurpolymj.2017.05.044.

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14

Alsaiari, Raiedhah A. "Supported Ruthenium and Tetrapropylammonium Bromide Catalysts for Oxidative Carboxylation of 1-Decene." Asian Journal of Chemistry 32, no. 4 (2020): 771–75. http://dx.doi.org/10.14233/ajchem.2020.22350.

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Cyclic carbonate compounds are valuable for a range of applications and can be synthesized by a one-pot reaction involving epoxidation of olefin followed by reaction of the epoxide with CO2. This study used supported ruthenium catalysts for the epoxidation step (first step), where a combination of tetrapropylammonium bromide and zinc bromide was used for the cycloaddition of carbon dioxide. The supported ruthenium catalyst, prepared by a sol-immobilization method, allowed the effective epoxidation of 1-decene in air (using oxygen as the main oxidant) at 90 ºC in the presence of a catalytic quantity of radical initiator. This approach was applied to the one-pot multi-step oxidative carboxylation of 1-decene in the presence of 1 % Ru/support-Pr4NBr/ZnBr2 catalyst

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15

Hanifpour, Ahad, Naeimeh Bahri-Laleh, Mehdi Nekoomanesh-Haghighi, and Albert Poater. "Group IV diamine bis(phenolate) catalysts for 1-decene oligomerization." Molecular Catalysis 493 (September 2020): 111047. http://dx.doi.org/10.1016/j.mcat.2020.111047.

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16

GOLUBCHENKO, I., P. GALICH, V. KHRANOVSKAYA, and V. MOTORNYI. "Alkylation of phenol by n-decene-1 on deprotonized aluminosilicates." Petroleum Chemistry U.S.S.R. 28, no. 3 (1988): 192–96. http://dx.doi.org/10.1016/0031-6458(88)90044-5.

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17

Xu, J. T., F. Wu, Z. Q. Fan, and A. J. Ryan. "PHASE SEPARATION IN THE MELT OF POLYPROPYLENE–1-DECENE COPOLYMERS." Journal of Macromolecular Science, Part B 41, no. 4-6 (2002): 1331–48. http://dx.doi.org/10.1081/mb-120013103.

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18

Khatuntsev, I. I., E. V. Pastushenko, D. �. Kruglov, and A. B. Terent'ev. "Homolytic addition of 2-ethoxy-1,3-dioxolane to 1-decene." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 9 (1985): 1892–94. http://dx.doi.org/10.1007/bf00953931.

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19

Anachkov, M. P., S. K. Rakovsky, R. K. Fotty, and A. K. Stoyanov. "DSC study of the thermal decomposition of 1-decene ozonide." Thermochimica Acta 237, no. 1 (1994): 213–17. http://dx.doi.org/10.1016/0040-6031(94)85202-2.

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20

Escher, Fernanda F. Nunes, Griselda Barrera Galland, and M�rcio Ferreira. "13Carbon nuclear magnetic resonance of ethylene-propylene-1-decene terpolymers." Journal of Polymer Science Part A: Polymer Chemistry 41, no. 16 (2003): 2531–41. http://dx.doi.org/10.1002/pola.10790.

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21

Long, Gregory S., Benjamin Snedeker, Kyle Bartosh, Michelle L. Werner, and Ayusman Sen. "Transition metal phthalocyanine and porphyrin complexes as catalysts for the polymerization of alkenes." Canadian Journal of Chemistry 79, no. 5-6 (2001): 1026–29. http://dx.doi.org/10.1139/v01-079.

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Vanadium phthalocyanine and porphyrin complexes, in conjunction with methylaluminoxane (MAO) or EtAlCl2 cocatalyst, have been found to catalyze the homopolymerization of ethene. In addition, the copolymerization of ethene with propene and 1-decene was achieved with the vanadium phthalocyanine complex and MAO. Nickel phthalocyanine complex was also found to catalyze the polymerization of ethene in the presence of MAO. However, only dimerization was observed when EtAlCl2 was used as the cocatalyst.Key words: phthalocyanine, porphyrin, polymerization, copolymerization, ethene, propene, 1-decene.

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22

Li, Pei, Xiaotian Li, Shabnam Behzadi та ін. "Living Chain-Walking (Co)Polymerization of Propylene and 1-Decene by Nickel α-Diimine Catalysts". Polymers 12, № 9 (2020): 1988. http://dx.doi.org/10.3390/polym12091988.

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Homo- and copolymers of propylene and 1-decene were synthesized by controlled chain-walking (co)polymerization using phenyl substituted α-diimine nickel complexes activated with modified methylaluminoxane (MMAO). This catalytic system was found to polymerize propylene in a living fashion to furnish high molecular weight ethylene-propylene (EP) copolymers. The copolymerizations proceeded to give high molecular weight P/1-decene copolymers with narrow molecular weight distribution (Mw/Mn ≈ 1.2), which indicated a living nature of copolymerization at room temperature. The random copolymerization results indicated the possibility of precise branched structure control, depending on the polymerization temperature and time.

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23

Zhou, Cunhui, Wenqian Li, Minghuang Qiu, et al. "Precisely regulating the acidity of mesoporous silica on the catalytic performance of 1-decene oligomerization." New Journal of Chemistry 45, no. 20 (2021): 9109–17. http://dx.doi.org/10.1039/d1nj00279a.

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24

Matyska, Bohumír, Alena Dosedlová, Lidmila Petrusová та Hynek Balcar. "Cometathesis of methyl oleate with α-olefins". Collection of Czechoslovak Chemical Communications 54, № 2 (1989): 455–61. http://dx.doi.org/10.1135/cccc19890455.

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Cometathesis of methyl oleate with 1-hexene or with other α-olefins affords two new esters and two new olefins. In the case of 1-hexene these products are methyl 9-decenoate, methyl 9-tetradecenoate, 1-decene and 5-tetradecene. At the same time, the formation of the esters and olefins with shorter chains(i.e. decene and decenoate) is distinctly preffered. Obviously, the transfer of methylene group from the alkene to the ester molecule is much easier than that of the alkylidene moiety. The non-stoichiometric course of cometathesis is associated with the carbene mechanism of the reaction.

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25

Tekawade, Aniket, Tianbo Xie, and Matthew A. Oehlschlaeger. "Comparative Study of the Ignition of 1-Decene, trans-5-Decene, and n-Decane: Constant-Volume Spray and Shock-Tube Experiments." Energy & Fuels 31, no. 6 (2017): 6493–500. http://dx.doi.org/10.1021/acs.energyfuels.7b00430.

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26

Pagar, N. S., and R. M. Deshpande. "Solubility of Hydrogen, Carbon Monoxide and 1-Decene in Water, Toluene and Water-N-methyl-2-pyrrolidone Biphasic Solvent Mixtures." Asian Journal of Chemistry 36, no. 5 (2024): 1178–82. http://dx.doi.org/10.14233/ajchem.2024.31434.

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The solubility of carbon monoxide and hydrogen has been determined experimentally as a function of their pressure in toluene, water and water-N-methyl-2-pyrrolidone (70:30 v/v) mixtures in the 383-403 K temperature range. The value of Henry’s constant for hydrogen and carbon monoxide was determined in all three solvent systems. Pressure had a linear influence on all systems, as predicted by Henry’s law. Through experimentation, the solubility of 1-decene in the organic and aqueous phase was established. The experimental data for the liquid-liquid equilibrium of 1-decene in a toluene and water-N-methyl-2-pyrrolidone mixture has been evaluated in the temperature range of 383-403 K. Temperature has a negligible effect on 1-decene solubility in the aqueous phase, but a significant effect in water-N-methyl-2-pyrrolidone (70:30 v/v) combination. The study of the solubility of hydrogen and carbon monoxide in organic and water-N-methyl-2-pyrrolidone mixture can be used for the kinetic study.

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27

Chinnathambi, Shanmugavel, Subramani Karthikeyan, Nobutaka Hanagata, and Naoto Shirahata. "Molecular interaction of silicon quantum dot micelles with plasma proteins: hemoglobin and thrombin." RSC Advances 9, no. 26 (2019): 14928–36. http://dx.doi.org/10.1039/c9ra02829c.

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28

Kosuri, Madhava R., Henry Gerung, Qiming Li, Sang M. Han, Paulo E. Herrera-Morales, and Jason F. Weaver. "Vapor-phase adsorption kinetics of 1-decene on hydrogenated Si(111)." Surface Science 596, no. 1-3 (2005): 21–38. http://dx.doi.org/10.1016/j.susc.2005.08.021.

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29

Engel, Rebecca V., Raiedhah Alsaiari, Ewa Nowicka, et al. "Solvent-free aerobic epoxidation of 1-decene using supported cobalt catalysts." Catalysis Today 333 (August 2019): 154–60. http://dx.doi.org/10.1016/j.cattod.2018.09.005.

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30

Tada, Akio, Hiroyasu Suzuka, and Yuzo Imizu. "Boron Phosphate as a Highly Active Catalyst for 1-Decene Oligomerization." Chemistry Letters 16, no. 2 (1987): 423–24. http://dx.doi.org/10.1246/cl.1987.423.

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31

Jiang, Hongbo, and Kaijian Yu. "Catalytic polymerization of 1-decene using a silicon-bridged metallocene system." Petroleum Science and Technology 35, no. 14 (2017): 1451–56. http://dx.doi.org/10.1080/10916466.2017.1344706.

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32

Ohno, Teruhisa, Yuji Masaki, Seiko Hirayama, and Michio Matsumura. "TiO2-Photocatalyzed Epoxidation of 1-Decene by H2O2 under Visible Light." Journal of Catalysis 204, no. 1 (2001): 163–68. http://dx.doi.org/10.1006/jcat.2001.3384.

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33

Gerlach, Martin, Sabine Kirschtowski, Andreas Seidel‐Morgenstern, and Christof Hamel. "Kinetic Modeling of the Palladium‐Catalyzed Isomerizing Methoxycarbonylation of 1‐Decene." Chemie Ingenieur Technik 90, no. 5 (2018): 673–78. http://dx.doi.org/10.1002/cite.201700162.

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34

Peña, Begoña, Juan A. Delgado, Ernesto Pérez, and Antonio Bello. "Monomer sequence distributions in the copolymerization of ethylene and 1-decene." Macromolecular Chemistry and Physics 195, no. 7 (1994): 2457–67. http://dx.doi.org/10.1002/macp.1994.021950714.

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35

Doskočilová, Danica, Jan Pecka, Jiří Dybal, Jaroslav Kříž, and František Mikeš. "Spectroscopic study of 1-decene oligomers obtained with AlCl3 as catalyst." Macromolecular Chemistry and Physics 195, no. 8 (1994): 2747–58. http://dx.doi.org/10.1002/macp.1994.021950806.

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36

Wang, Yan, Xihui Ge, Minqing Zhang, Huaigong Zhu, Zijian Zhang, and Ming Wang. "Growth characteristic, guest distribution, guest ordering and the stability of urea inclusion compounds with 1-decene, n-decane and mixture of 1-decene and n-decane." Journal of Molecular Structure 1058 (January 2014): 259–64. http://dx.doi.org/10.1016/j.molstruc.2013.11.021.

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37

Jayakumar, S. Venkatesan, and Divya Rana Tomar. "Synthesis and Comparison of Reactivity of Amine-Borane Complexes." Oriental Journal Of Chemistry 40, no. 6 (2024): 1709–14. https://doi.org/10.13005/ojc/400623.

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The present study emphasizes on synthesis and characterization of three ABs: Aniline-Borane (AAB), Triethylamine-Borane (TAB), and N,N-Dimethylaniline-Borane (DMAB). The AB reagents were characterized by 11B-NMR spectra and new green procedure was developed to determine the active borane concentration by gasometer. Furthermore, the reactivity of AB complexes has been compared against 1-decene under microwave and ultrasound radiation for the first time. The outcome of gasometer and microwave, ultrasound reactions revealed that TAB is extremely stable and inert. Whereas AAB release borane species rapidly and complete the hydroboration of 1-decene.

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38

Baek, Jun Won, Young Bin Hyun, Hyun Ju Lee та ін. "Selective Trimerization of α-Olefins with Immobilized Chromium Catalyst for Lubricant Base Oils". Catalysts 10, № 9 (2020): 990. http://dx.doi.org/10.3390/catal10090990.

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The demand for poly(α-olefin)s (PAOs), which are high-performance group IV lubricant base oils, is increasingly high. PAOs are generally produced via the cationic oligomerization of 1-decene, wherein skeleton rearrangement inevitably occurs in the products. Hence, a transition-metal-based catalytic process that avoids rearrangement would be a valuable alternative for cationic oligomerization. In particular, transition-metal-catalyzed selective trimerization of α-olefins has the potential for success. In this study, (N,N′,N″-tridodecyltriazacyclohexane)CrCl3 complex was reacted with MAO-silica (MAO, methylaluminoxane) for the preparation of a supported catalyst, which exhibited superior performance in selective α-olefin trimerization compared to that of the corresponding homogeneous catalyst, enabling the preparation of α-olefin trimers at ~200 g scale. Following hydrogenation, the prepared 1-decene trimer (C30H62) exhibited better lubricant properties than those of commercial-grade PAO-4 (kinematic viscosity at 40 °C, 15.1 vs. 17.4 cSt; kinematic viscosity at 100 °C, 3.9 vs. 3.9 cSt; viscosity index, 161 vs. 123). Moreover, it was shown that 1-octene/1-dodecene mixed co-trimers (i.e., a mixture of C24H50, C28H58, C32H66, and C36H74), generated by the selective supported Cr catalyst, exhibited outstanding lubricant properties analogous to those observed for the 1-decene trimer (C30H62).

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39

Echaroj, Snunkheam, Channarong Asavatesanupap, Sumaeth Chavadej, and Malee Santikunaporn. "Kinetic Study on Microwave-Assisted Oligomerization of 1-Decene over a HY Catalyst." Catalysts 11, no. 9 (2021): 1105. http://dx.doi.org/10.3390/catal11091105.

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A promising production route for a high-quality base stock for lubricants is the oligomerization of high molecular-weight olefins in a high energy efficiency system. Oligomerization of 1-decene (C10) was conducted in a microwave-assisted system over a HY zeolite catalyst at different reaction temperatures and times. Higher reaction temperature resulted in increasing formation of dimers and trimers. The oligomerization reaction yielded 80% conversion, 54.2% dimer product, 22.3% trimer product and 3.4% heavier product at 483 K for a reaction time of 3 h. The best fit kinetic model for the dimerization reaction was formulated from an assumption of no vacant reaction sites. For the trimerization reaction, a molecule of dimer (C20) formed on the active site, interacted with a molecule of 1-decene in the bulk solution to form a molecule of trimer (C30). Apparent activation energies for the dimerization and trimerization reactions were 70.8 ± 0.8 and 83.6 ± 0.9 kJ/mol, respectively. The C13-NMR spectrum indicated that the oligomer product contained a significant portion of highly branched hydrocarbons, causing a substantial reduction in the viscosity index compared to conventional poly-alpha olefin lubricant (PAO).

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40

Isakov, Elkhan U., Jeyhun Sh Hamidova, and Elnara I. Hasanova. "Synthesis of Copolymers of Decylmethacrylate with Decene-1 as a Viscosity Additive." Open Journal of Yangtze Oil and Gas 02, no. 02 (2017): 82–91. http://dx.doi.org/10.4236/ojogas.2017.22006.

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41

Kosuri, Madhava R., Henry Gerung, Qiming Li, Sang M. Han, Bruce C. Bunker, and Thomas M. Mayer. "Vapor-Phase Adsorption Kinetics of 1-Decene on H-Terminated Si(100)." Langmuir 19, no. 22 (2003): 9315–20. http://dx.doi.org/10.1021/la035153p.

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42

Dressier, F. H., and S. Vermaire. "The cationic oligomerization of C10 fischer-tropsch olefins and of 1-decene." Makromolekulare Chemie. Macromolecular Symposia 13-14, no. 1 (1988): 271–87. http://dx.doi.org/10.1002/masy.19880130120.

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43

Vaganov, R. A., N. V. Deryagina, and F. A. Buryukin. "Extraction Octene-1 and Decene-1 from C8+ Fraction by Production of Linear Alpha- Olefins." Journal of Siberian Federal University. Chemistry 8, no. 3 (2015): 327–35. http://dx.doi.org/10.17516/1998-2836-2015-8-3-327-335.

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44

Kohls, Emilija, and Matthias Stein. "The thermochemistry of long chain olefin isomers during hydroformylation." New Journal of Chemistry 41, no. 15 (2017): 7347–55. http://dx.doi.org/10.1039/c7nj01396e.

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45

Klenner, Mitchell A., Marina Cagnes, Kathleen Wood, Kazuki Mita, Mizuki Kishimoto, and Tamim Darwish. "Decagram scale production of deuterated mineral oil and polydecene as solvents for polymer studies in neutron scattering." Polymer Chemistry 11, no. 31 (2020): 4986–94. http://dx.doi.org/10.1039/d0py00690d.

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46

Grosjean, Eric, Daniel Grosjean, and John H. Seinfeld. "Atmospheric Chemistry of 1-Octene, 1-Decene, and Cyclohexene: Gas-Phase Carbonyl and Peroxyacyl Nitrate Products." Environmental Science & Technology 30, no. 3 (1996): 1038–47. http://dx.doi.org/10.1021/es950592z.

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47

Cho, Dong Woo, Jungin Shin, Won Bae, Hwayong Kim, and Kyung Won Seo. "High-Pressure Phase Behavior of Heptadecafluoro-1-decene and Nonafluoro-1-hexene in Supercritical Carbon Dioxide." Journal of Chemical & Engineering Data 57, no. 6 (2012): 1745–50. http://dx.doi.org/10.1021/je300258z.

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48

Wasserscheid, Peter, Siegfried Grimm, Randolf D. Köhn, and Matthias Haufe. "Synthesis of Synthetic Lubricants by Trimerization of 1-Decene and 1-Dodecene with Homogeneous Chromium Catalysts." Advanced Synthesis & Catalysis 343, no. 8 (2001): 814–18. http://dx.doi.org/10.1002/1615-4169(20011231)343:8<814::aid-adsc814>3.0.co;2-h.

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49

Seppälä, J. V., J. Koivumäki, and X. Liu. "Co- and terpolymerization of ethylene with 1-butene and 1-decene by using Cp2ZrCl2-methylaluminoxane catalyst." Journal of Polymer Science Part A: Polymer Chemistry 31, no. 13 (1993): 3447–52. http://dx.doi.org/10.1002/pola.1993.080311334.

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50

Bazanov, T. A., L. V. Petrov, B. L. Psikha, S. B. Psikha, V. M. Solyanikov, and V. V. Kharitonov. "Kinetics and mechanism of the oxidation of the products of decene-1 oligomerization." Russian Journal of Physical Chemistry B 3, no. 4 (2009): 567–72. http://dx.doi.org/10.1134/s1990793109040083.

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