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Journal articles on the topic 'Durene'

Author: Grafiati

Published: 4 June 2021

Last updated: 14 February 2022

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1

Zeller, Matthias, and Allen D. Hunter. "Bis(dimethylphosphorylmethyl)durene." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (2007): o802—o803. http://dx.doi.org/10.1107/s160053680700236x.

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2

Wijesekera, Tilak P., Shantha David, John B. Paine III, Brian R. James, and David Dolphin. "Durene-capped porphyrins: synthesis and characterization." Canadian Journal of Chemistry 66, no. 8 (1988): 2063–71. http://dx.doi.org/10.1139/v88-331.

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The synthesis of porphyrins having a fully hydrophobic cavity capped by a durene moiety is described. The size of the cavity is adjusted by varying the number of methylene -(CH2)n- groups linking the tetramethylphenylene cap with the diametrically opposite β-positions of the porphyrin. Bis(chloromethyl)durene (1) was first converted to durene-bisalkanoic acids 11 (n = 4), 13 (n = 5), and 18 (n = 7) using standard chain extension methods. The diacid chlorides were then used to acylate two equivalents of a β-unsubstituted pyrrole to give a chain-linked bispyrrole. Each pyrrole, following appropr

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3

Cheng, Si-Xue, Tai-Shung Chung, Rong Wang, and Rohit H. Vora. "Gas-sorption properties of 6FDA-durene/1,4-phenylenediamine (pPDA) and 6FDA-durene/1,3-phenylenediamine (mPDA) copolyimides." Journal of Applied Polymer Science 90, no. 8 (2003): 2187–93. http://dx.doi.org/10.1002/app.12874.

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4

Zaraiskii, A. P., L. I. Velichko, N. A. Zaraiskaya, and N. M. Anikeeva. "Exhaustive direct methylthiomethylation of mesitylene and durene." Russian Journal of General Chemistry 77, no. 1 (2007): 149. http://dx.doi.org/10.1134/s1070363207010239.

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5

LINDROOS, AARNE, SISKO MARIA ESKOLA, and FOLKE STENMAN. "Raman scattering from the iodine—durene complex." Molecular Physics 88, no. 5 (1996): 1217–22. http://dx.doi.org/10.1080/00268979609484506.

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6

LINDROOS, AARNE. "Raman scattering from the iodine-durene complex." Molecular Physics 88, no. 5 (1996): 1217–22. http://dx.doi.org/10.1080/00268979650025786.

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7

David, Shantha, Brian R. James, and David Dolphin. "Durene-capped porphyrin complexes of iron(II)." Journal of Inorganic Biochemistry 28, no. 2-3 (1986): 125–35. http://dx.doi.org/10.1016/0162-0134(86)80076-9.

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8

Travers, C., F. Raatz, and C. Marcilly. "Removal of durene from gasolines and kerosines." Zeolites 11, no. 2 (1991): 196. http://dx.doi.org/10.1016/0144-2449(91)80437-5.

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9

Emmanuel, M. O. "The structural aspects of durene–thiourea inclusion complex." Acta Crystallographica Section A Foundations of Crystallography 52, a1 (1996): C279. http://dx.doi.org/10.1107/s0108767396088332.

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10

David, Shantha, Brian R. James, and David Dolphin. "Binding of isocyanides to five-coordinate, durene-capped hemes." Canadian Journal of Chemistry 65, no. 5 (1987): 1098–102. http://dx.doi.org/10.1139/v87-184.

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Solution data at 20 °C are presented for the binding of t-butylisocyanide and tosylmethylisocyanide (TMIC) to the five-coordinate hemes Fe(porp)(Cy2Im), where Cy2Im = 1,5-dicyclohexylimidazole and porp = the dianion of some durene-capped porphyrins with variable length linking methylene straps on either side of the durene moiety (4/4, 5/5, or 7/7 methylenes). The tBuNC and TMIC ligands are used to probe the steric nature of the distal binding site under the cap, in particular the respective "central" and "peripheral" effects as defined by Traylor etal. The binding constants range from 1.1 × 10

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11

Lok, Chen Chuang, and Yin Fong Yeong. "Synthesis and Characterization of ZIF-8 Mixed Matrix Membranes." Applied Mechanics and Materials 625 (September 2014): 661–64. http://dx.doi.org/10.4028/www.scientific.net/amm.625.661.

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In the present work, ZIF-8/6FDA-durene mixed matrix membranes (MMMs) were synthesized and characterized. ZIF-8 nanocrystals, which were used as the inorganic filler, were synthesized using rapid room-temperature synthesis method whereas 6FDA-durene polyimide was synthesized by polycondensation method followed by chemical imidization. Pure and 6FDA-durene membranes loaded with 5 wt%, 10 wt% and 15 wt% of ZIF-8 were fabricated. The structural properties and morphology of the resultant membranes were characterized by using X-ray Diffraction (XRD) and Field emission scanning electron microscope (F

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12

Motta, Carlo, and Stefano Sanvito. "Charge Transport Properties of Durene Crystals from First-Principles." Journal of Chemical Theory and Computation 10, no. 10 (2014): 4624–32. http://dx.doi.org/10.1021/ct500390a.

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13

Yablokov, M. Yu, A. B. Gil’man, N. M. Surin, I. V. Semenov, A. A. Kuznetsov, and I. A. Chmutin. "Polymerization of 1,2,4,5-tetramethylbenzene (durene) in direct-current discharge." High Energy Chemistry 44, no. 5 (2010): 431–35. http://dx.doi.org/10.1134/s0018143910050140.

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14

Santhana Gopala Krishnan, P., R. H. Vora, and S. Veeramani. "Thermal degradation kinetics of 6FDA/durene diamine/pPDA copolyimides." Plastics, Rubber and Composites 31, no. 7 (2002): 289–94. http://dx.doi.org/10.1179/146580102225003146.

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15

DE GROOT, M. S., I. A. M. HESSELMANN, J. SCHMIDT, and J. H. VAN DER WAALS. "Optical pumping in an organic crystal: quinoxaline in durene." Molecular Physics 100, no. 1 (2002): 31–43. http://dx.doi.org/10.1080/00268970110088866.

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16

Kato, Masahiro, and Daisuke Kodama. "Vapor−Liquid Equilibrium of Durene in Methanol or Ethanol." Journal of Chemical & Engineering Data 49, no. 5 (2004): 1247–48. http://dx.doi.org/10.1021/je034227w.

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17

Cong, Shan, Ying Liu, Hong Li, Xingang Li, Lvhong Zhang, and Lei Wang. "Purification and separation of durene by static melt crystallization." Chinese Journal of Chemical Engineering 23, no. 3 (2015): 505–9. http://dx.doi.org/10.1016/j.cjche.2014.11.018.

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18

Ortmann, F., K. Hannewald, and F. Bechstedt. "Electronic properties of durene crystals: Implications for charge transport." physica status solidi (b) 245, no. 5 (2008): 825–29. http://dx.doi.org/10.1002/pssb.200743427.

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19

BARCLAY, G. G., J. P. CANDLIN, W. LAWRIE, and P. L. PAUSON. "ChemInform Abstract: Amino, Aminophenoxy and Aminobenzoyl Derivatives of Durene." ChemInform 23, no. 48 (2010): no. http://dx.doi.org/10.1002/chin.199248142.

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20

Reichert, Detlef, Guenter Hempel, Raphy Poupko, Zeev Luz, Zbiegniew Olejniczak, and Piotr Tekely. "MAS NMR studies of carbon-13 spin exchange in durene." Solid State Nuclear Magnetic Resonance 13, no. 3 (1998): 137–48. http://dx.doi.org/10.1016/s0926-2040(98)00085-x.

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21

Yamauchi, Seigo, Masahide Terazima, and Noboru Hirota. "Photochemical reaction of quinoxaline in a single crystal of durene." Journal of Physical Chemistry 89, no. 22 (1985): 4804–8. http://dx.doi.org/10.1021/j100268a029.

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22

Chung, Tai-Shung, Wen-Hui Lin, and Rohit H. Vora. "Gas transport properties of 6FDA-durene/1,3-phenylenediamine (mPDA) copolyimides." Journal of Applied Polymer Science 81, no. 14 (2001): 3552–64. http://dx.doi.org/10.1002/app.1812.

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23

Lin, Wen-Hui, Rohit H. Vora, and Tai-Shung Chung. "Gas transport properties of 6FDA-durene/1,4-phenylenediamine (pPDA) copolyimides." Journal of Polymer Science Part B: Polymer Physics 38, no. 21 (2000): 2703–13. http://dx.doi.org/10.1002/1099-0488(20001101)38:21<2703::aid-polb10>3.0.co;2-b.

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24

Ligocka, D., A. Sapota, and K. Rydzynski. "The disposition and metabolism of durene (1,2,4,5-tetramethylbenzene) in rats." Archives of Toxicology 74, no. 11 (2001): 673–79. http://dx.doi.org/10.1007/s002040000165.

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25

Kammakakam, Irshad, SangYong Nam, and Tae-Hyun Kim. "PEG–imidazolium-functionalized 6FDA–durene polyimide as a novel polymeric membrane for enhanced CO2 separation." RSC Advances 6, no. 37 (2016): 31083–91. http://dx.doi.org/10.1039/c6ra00735j.

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26

Rutherford, J. S., E. Marfo-Owusu, P. S. Ford, and J. A. K. Howard. "Monoclinic thiourea inclusion complexes: implications of the durene adduct crystal structure." Acta Crystallographica Section A Foundations of Crystallography 52, a1 (1996): C281. http://dx.doi.org/10.1107/s0108767396088265.

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27

Hossain, Iqubal, Abu Zafar Al Munsur, Ook Choi, and Tae-Hyun Kim. "Bisimidazolium PEG-mediated crosslinked 6FDA-durene polyimide membranes for CO2 separation." Separation and Purification Technology 224 (October 2019): 180–88. http://dx.doi.org/10.1016/j.seppur.2019.05.014.

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28

Ortmann, Frank, Karsten Hannewald, and Friedhelm Bechstedt. "Ab initio description and visualization of charge transport in durene crystals." Applied Physics Letters 93, no. 22 (2008): 222105. http://dx.doi.org/10.1063/1.3033830.

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29

Wang, Rong, Yiming Cao, Rohit Vora, and Robert J. Tucker. "Fabrication of 6FDA-durene polyimide asymmetric hollow fibers for gas separation." Journal of Applied Polymer Science 82, no. 9 (2001): 2166–73. http://dx.doi.org/10.1002/app.2064.

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30

Lin, Wen-Hui, and Tai-Shung Chung. "The physical aging phenomenon of 6FDA-durene polyimide hollow fiber membranes." Journal of Polymer Science Part B: Polymer Physics 38, no. 5 (2000): 765–75. http://dx.doi.org/10.1002/(sici)1099-0488(20000301)38:5<765::aid-polb14>3.0.co;2-h.

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31

Kobashi, Harumichi, Tomoyuki Kondo, and Masa-aki Funabashi. "Solvent Effect on Lifetime of Triplet Exciplex between Chloranil and Durene." Bulletin of the Chemical Society of Japan 59, no. 7 (1986): 2347–48. http://dx.doi.org/10.1246/bcsj.59.2347.

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32

Hossain, Iqubal, Abu Al Munsur, and Tae-Hyun Kim. "A Facile Synthesis of (PIM-Polyimide)-(6FDA-Durene-Polyimide) Copolymer as Novel Polymer Membranes for CO2 Separation." Membranes 9, no. 9 (2019): 113. http://dx.doi.org/10.3390/membranes9090113.

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Random copolymers made of both (PIM-polyimide) and (6FDA-durene-PI) were prepared for the first time by a facile one-step polycondensation reaction. By combining the highly porous and contorted structure of PIM (polymers with intrinsic microporosity) and high thermomechanical properties of PI (polyimide), the membranes obtained from these random copolymers [(PIM-PI)-(6FDA-durene-PI)] showed high CO2 permeability (>1047 Barrer) with moderate CO2/N2 (> 16.5) and CO2/CH4 (> 18) selectivity, together with excellent thermal and mechanical properties. The membranes prepared from three diffe

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33

Kammakakam, Irshad, SangYong Nam, and Tae-Hyun Kim. "Ionic group-mediated crosslinked polyimide membranes for enhanced CO2 separation." RSC Advances 5, no. 86 (2015): 69907–14. http://dx.doi.org/10.1039/c5ra13081f.

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34

Lischiner, I. I., O. V. Malova, A. L. Tarasov, M. F. Krotov, S. V. Korobtsev, and B. V. Potapkin. "Obtaining of Environmental Motor Fuel with Low Durene Content of Dimethyl Ether." Ecology and Industry of Russia 21, no. 2 (2017): 20–23. http://dx.doi.org/10.18412/1816-0395-2017-2-20-23.

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35

Liu, S. L., R. Wang, Y. Liu, M. L. Chng, and T. S. Chung. "The physical and gas permeation properties of 6FDA-durene/2,6-diaminotoluene copolyimides." Polymer 42, no. 21 (2001): 8847–55. http://dx.doi.org/10.1016/s0032-3861(01)00439-6.

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36

Cameron, Nicola E., Rachael A. Linklater, William Henderson, Brian K. Nicholson та T. S. Andy Hor. "Spanning [Pt2(μ-S)2(PPh3)4] metalloligands with 1,4-dimercurated durene". Journal of Organometallic Chemistry 693, № 25 (2008): 3711–14. http://dx.doi.org/10.1016/j.jorganchem.2008.09.013.

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37

Rai, U. S., and Pinky Pandey. "Physical chemistry of binary organic eutectic and monotectic alloys; durene–pyrogallol system." Thermochimica Acta 364, no. 1-2 (2000): 111–19. http://dx.doi.org/10.1016/s0040-6031(00)00597-9.

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38

Nafisi, Vajiheh, and May-Britt Hägg. "Gas separation properties of ZIF-8/6FDA-durene diamine mixed matrix membrane." Separation and Purification Technology 128 (May 2014): 31–38. http://dx.doi.org/10.1016/j.seppur.2014.03.006.

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39

David, Shantha, Brian R. James, David Dolphin, Teddy G. Traylor, and Marco A. Lopez. "Dioxygen and carbon monoxide binding to apolar cyclophane hemes: durene-capped hemes." Journal of the American Chemical Society 116, no. 1 (1994): 6–14. http://dx.doi.org/10.1021/ja00080a002.

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40

Jung, Kyung-Hye, Nimanka Panapitiya, and John P. Ferraris. "Electrochemical energy storage performance of carbon nanofiber electrodes derived from 6FDA-durene." Nanotechnology 29, no. 27 (2018): 275701. http://dx.doi.org/10.1088/1361-6528/aabc9c.

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41

An, Heseong, Albert S. Lee, Irshad Kammakakam, et al. "Bromination/debromination-induced thermal crosslinking of 6FDA-Durene for aggressive gas separations." Journal of Membrane Science 545 (January 2018): 358–66. http://dx.doi.org/10.1016/j.memsci.2017.09.083.

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42

Lin, Wen-Hui, and Tai-Shung Chung. "Gas permeability, diffusivity, solubility, and aging characteristics of 6FDA-durene polyimide membranes." Journal of Membrane Science 186, no. 2 (2001): 183–93. http://dx.doi.org/10.1016/s0376-7388(01)00333-7.

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43

Peng, Mei Mei, Abidov Aziz, Muthiahpillai Palanichamy, and Seung Gil Lee. "Selective Cracking of Durene to Para-Dimethyl Benzene over ZSM-5 Zeolite." International Journal of Control and Automation 6, no. 5 (2013): 181–90. http://dx.doi.org/10.14257/ijca.2013.6.5.17.

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44

Lefebvre, J., A. Miniewicz, and R. Kowal. "Structure of the 1:1 molecular complex of durene with 1,2,4,5-tetracyanobenzene." Acta Crystallographica Section C Crystal Structure Communications 45, no. 9 (1989): 1372–76. http://dx.doi.org/10.1107/s0108270189001009.

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45

Li, Maijun, Zhibo Zheng, Zhiguang Zhang, et al. "“All Polyimide” Mixed Matrix Membranes for High Performance Gas Separation." Polymers 13, no. 8 (2021): 1329. http://dx.doi.org/10.3390/polym13081329.

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To improve the interfacial compatibility of mixed matrix membranes (MMMs) for gas separation, microporous polyimide particle (AP) was designed, synthesized, and introduced into intrinsic microporous polyimide matrix (6FDA-Durene) to form “all polyimide” MMMs. The AP fillers showed the feature of thermal stability, similar density with polyimide matrix, high porosity, high fractional free volume, large microporous dimension, and interpenetrating network architecture. As expected, the excellent interfacial compatibility between 6FDA-Durene and AP without obvious agglomeration even at a high AP l

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46

Indig, G. L., L. H. Catalani, and T. Wilson. "Quenching of triplet acetone by mesitylene and durene: exciplex formation or energy transfer?" Journal of Physical Chemistry 96, no. 22 (1992): 8967–73. http://dx.doi.org/10.1021/j100201a050.

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47

Clemens, Anthony H., John H. Ridd, and John P. B. Sandall. "15N nuclear polarisation in nitration and related reactions. Part 4. Durene and nitrodurene." Journal of the Chemical Society, Perkin Transactions 2, no. 8 (1985): 1227. http://dx.doi.org/10.1039/p29850001227.

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48

Radomska, M., and R. Radomski. "Phase diagrams in the binary systems of tetracyanoethylene with mesitylene, durene and pentamethylbenzene." Journal of Thermal Analysis 37, no. 4 (1991): 693–704. http://dx.doi.org/10.1007/bf01913148.

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49

Mac, Marek, Piotr Kwiatkowski, and Andrzej M. Turek. "Influence of temperature on fluorescence quenching of 9,10-dicyanoanthracene by durene in acetonitrile." Journal of Luminescence 65, no. 6 (1995): 341–48. http://dx.doi.org/10.1016/0022-2313(95)00079-8.

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50

Mashhadikhan, Samaneh, Abtin Ebadi Amooghin, Abdolreza Moghadassi, and Hamidreza Sanaeepur. "Functionalized filler/synthesized 6FDA-Durene high performance mixed matrix membrane for CO2 separation." Journal of Industrial and Engineering Chemistry 93 (January 2021): 482–94. http://dx.doi.org/10.1016/j.jiec.2020.10.033.

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