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Journal articles on the topic 'O-phenylenes'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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1

Vemuri, Gopi Nath, Meng Chu, Han Dong, Brian J. Spinello, and C. Scott Hartley. "Solvent effects on the folding of o-phenylene oligomers." Organic & Biomolecular Chemistry 15, no. 4 (2017): 845–51. http://dx.doi.org/10.1039/c6ob02512a.

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2

Kasun, Zachary A., Hiroki Sato, Jing Nie, et al. "Alternating oligo(o,p-phenylenes) via ruthenium catalyzed diol–diene benzannulation: orthogonality to cross-coupling enables de novo nanographene and PAH construction." Chemical Science 9, no. 40 (2018): 7866–73. http://dx.doi.org/10.1039/c8sc03236j.

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3

Vemuri, Gopi Nath, Rathiesh R. Pandian, Brian J. Spinello, Erika B. Stopler, Zacharias J. Kinney, and C. Scott Hartley. "Twist sense control in terminally functionalized ortho-phenylenes." Chemical Science 9, no. 43 (2018): 8260–70. http://dx.doi.org/10.1039/c8sc02821d.

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4

Marqués-González, Santiago, Shintaro Fujii, Tomoaki Nishino, et al. "Scanning tunnelling microscopy analysis of octameric o-phenylenes on Au(111)." RSC Advances 6, no. 61 (2016): 55970–75. http://dx.doi.org/10.1039/c6ra07173b.

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STM microscopy allowed direct observation of perfectly- and partially-folded conformers of OP<sub>8</sub>Br and OP<sub>8</sub>NO<sub>2</sub>on Au(111). The metastable partially-folded conformation was stabilized by their more efficient electronic coupling with the Au substrate.

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5

Rajca, Andrzej, Hua Wang, Pavel Bolshov та Suchada Rajca. "A Greek cross dodecaphenylene: sparteine-mediated asymmetric synthesis of chiral D2-symmetric π-conjugated tetra-o-phenylenes". Tetrahedron 57, № 17 (2001): 3725–35. http://dx.doi.org/10.1016/s0040-4020(01)00241-1.

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6

Wu, Li, Xue-Fang Shi, Zhi-Yong Xing, and Wen-Qin Zhang. "o-Phenylene bis(benzenesulfonate)." Acta Crystallographica Section E Structure Reports Online 61, no. 11 (2005): o3684—o3685. http://dx.doi.org/10.1107/s1600536805032332.

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7

Kawahara, Tetsuro, Taketoshi Kuroda, Hideo Matsui, et al. "Electronic properties of calcined materials from a scandium-O-phenylene-O-yttrium-O-phenylene hybrid copolymer." Journal of Materials Science 42, no. 11 (2007): 3708–13. http://dx.doi.org/10.1007/s10853-006-0394-z.

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8

Lee, Eung-Jae, Doo-Soo Yoon, and Jae-Kon Choi. "Synthesis and Thermal Properties of Aromatic Poly(o-hydroxyamide)s Containing Phenylene Diimide Unit." Journal of the Korea Academia-Industrial cooperation Society 14, no. 11 (2013): 6029–38. http://dx.doi.org/10.5762/kais.2013.14.11.6029.

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9

Matsui, H., S. Yamamoto, R. Ito, S. Karuppuchamy, and M. Yoshihara. "The electronic behavior of calcined material obtained from an (yttrium-O-phenylene-O)–(ytterbium-O-phenylene-O) hybrid copolymer." Journal of Alloys and Compounds 472, no. 1-2 (2009): L13—L17. http://dx.doi.org/10.1016/j.jallcom.2008.05.001.

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10

Li, Qi, and Wei-jian Xue. "(3,6-Dibromo-o-phenylene)dimethanol." Acta Crystallographica Section E Structure Reports Online 67, no. 2 (2011): o400. http://dx.doi.org/10.1107/s1600536811001206.

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11

Bryan, Jeffrey C., Jay M. Rosenberg, and Konstantinos Kavallieratos. "N,N′-(o-Phenylene)dibenzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 61, no. 2 (2005): o396—o397. http://dx.doi.org/10.1107/s1600536805001133.

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12

Niu, Jun-long, Xia Wang, Biao Gao, and Mao-ping Song. "O,O′-2-Iodo-1,3-phenylene bis(diphenylphosphinothioate)." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2499. http://dx.doi.org/10.1107/s1600536811033629.

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13

Malzkuhn, Sabine, Xingwei Guo, Daniel Häussinger, and Oliver S. Wenger. "Electron Transfer across o-Phenylene Wires." Journal of Physical Chemistry A 123, no. 1 (2018): 96–102. http://dx.doi.org/10.1021/acs.jpca.8b11236.

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14

Chattopadhyay, Basab, Sharmila Basu, Somnath Ghosh, Madeleine Helliwell, and Monika Mukherjee. "2,2′-Diazinodimethylidyne)di-o-phenylene) dibenzoate." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (2008): o866. http://dx.doi.org/10.1107/s1600536808010155.

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15

Saeed, Aamer, Naeem Abbas, Hummera Rafique, and Michael Bolte. "3,3′-Dibutanoyl-1,1′-(o-phenylene)dithiourea." Acta Crystallographica Section E Structure Reports Online 66, no. 2 (2010): o441. http://dx.doi.org/10.1107/s1600536810001789.

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16

Yang, Yu-Min. "[o-Phenylenebis(salicylideneaminato)]copper(II)." Acta Crystallographica Section E Structure Reports Online 61, no. 7 (2005): m1425—m1426. http://dx.doi.org/10.1107/s1600536805019975.

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17

Kawahata, Masatoshi, Kentaro Yamaguchi, Tomoya Ito, and Tsutomu Ishikawa. "2,2′-o-Phenylenebis(1,3-dimethylguanidine)." Acta Crystallographica Section E Structure Reports Online 62, no. 8 (2006): o3301—o3302. http://dx.doi.org/10.1107/s1600536806026365.

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18

Matsui, Hideo, Taketoshi Kuroda, Keigo Otsuki, et al. "Electronic behavior of calcined material from a tellurium-S-phenylene-O-strontium-O-phenylene-S hybrid copolymer." TANSO 2006, no. 222 (2006): 114–17. http://dx.doi.org/10.7209/tanso.2006.114.

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19

YAMAMOTO, Shin, Hideo MATSUI, Kosuke MATOBA, Subbian KARUPPUCHAMY, and Masakuni YOSHIHARA. "Electronic Behavior of Calcined Material from a (Niobium-O-Phenylene-S) - (Cadmium-S-Phenylene-O) Hybrid Copolymer." Journal of the Japan Society of Colour Material 80, no. 6 (2007): 241–45. http://dx.doi.org/10.4011/shikizai1937.80.241.

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20

Sugimoto, Hideki, and Koji Tanaka. "Syntheses of new ruthenium carbonyl terpyridine o-phenylene complexes: strong interaction between carbonyl and o-phenylene ligands." Journal of Organometallic Chemistry 622, no. 1-2 (2001): 280–85. http://dx.doi.org/10.1016/s0022-328x(00)00941-4.

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21

Enyo, Tomonori, Nobuaki Arai, Norio Nakane, Athanassios Nicolaides, and Hideo Tomioka. "o-Phenylene Halocarbenonitrenes ando-Phenylene Chlorocarbenocarbene: A Combined Experimental and Computational Approach." Journal of Organic Chemistry 70, no. 19 (2005): 7744–54. http://dx.doi.org/10.1021/jo0512204.

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22

Krainova, Julia, Christopher Dares, and A. B. P. Lever. "4,4′-Dichloro-N,N′-(o-phenylene)dibenzenesulfonamide." Acta Crystallographica Section E Structure Reports Online 65, no. 1 (2008): o178. http://dx.doi.org/10.1107/s1600536808039718.

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23

Kwak, Han, Sea-Hyun Kim, Pan-Gi Kim, Cheal Kim, and Youngmee Kim. "N,N′-(4,5-Dichloro-o-phenylene)dibenzamide." Acta Crystallographica Section E Structure Reports Online 63, no. 7 (2007): o3141. http://dx.doi.org/10.1107/s160053680702733x.

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24

Booysen, Irvin, Thomas I. A. Gerber, Eric Hosten, and Peter Mayer. "2,2′-Diamino-N,N′-(o-phenylene)dibenzamide." Acta Crystallographica Section E Structure Reports Online 65, no. 4 (2009): o850. http://dx.doi.org/10.1107/s1600536809009283.

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25

Yamamoto, S., H. Matsui, S. Ishiyama, S. Karuppuchamy, and M. Yoshihara. "Electronic behavior of calcined material obtained from a tantalum-O-phenylene-S-tin-S-phenylene-O hybrid copolymer." Materials Science and Engineering: B 135, no. 2 (2006): 120–24. http://dx.doi.org/10.1016/j.mseb.2006.08.047.

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26

Plešek, Jaromír, та Stanislav Heřmánek. "The (η-1,7'-2,2')4,8'-8,4'-(Bis-μ-o-phenylene)bisdicarbollidocobalt(1-)ate Ion [3-Co-4,8'-8,4'(o-C6H4)2(1,2-C2B9H9)2](-). The First Doubly Bridged Metallacarborane Complex. Synthesis, Properties and Structure". Collection of Czechoslovak Chemical Communications 60, № 8 (1995): 1297–302. http://dx.doi.org/10.1135/cccc19951297.

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The first cobaltacarborane sandwich complex [3-Co-4,8'-8,4'(o-C6H4)2(1,2-C2B9H9)2](-) with two o-phenylene bridges between both deltahedral ligands is described. Phenylene rings containing angle of 72 grad bind the Cs counter-ion probably via π-donation. This is why the solubility of Cs salt in water is extremely low. Synthesis, properties and structure of the Cs salt are described.

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27

Abd El-Ghaffar, M. A., K. A. Shaffei, and Nourelhoda Abdelwahab. "Evaluation of Some Conducting Polymers as Novel Antioxidants for Rubber Vulcanizates." International Journal of Polymer Science 2014 (2014): 1–9. http://dx.doi.org/10.1155/2014/893542.

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Natural rubber (NR) and styrene-butadiene rubber (SBR) formulations containing polyaromatic and polyheterocyclic amine homopolymers and copolymers were prepared. The studied homopolymers named polythiophene (PT), poly(o-phenylene diamine) (Po-PDA) and copolymers named poly(aniline-co-m-toluidine) (PAn-co-mT), poly(aniline-co-o-phenylene diamine) (PAn-co-o-PDA), poly(aniline-co-thiophene) (PAn-co-T), poly(aniline-co-2-amino pyridine) (PAn-co-2APy), and poly(2-amino pyridine-co-o-phenylene diamine) (P2APy-co-o-PDA) have been prepared and characterized. The rheological characteristics and physico

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28

Feng, Jian-Shen, Li-Ke Zou, Bin Xie, Yang-Guang Xiang, and Chuan Lai. "(meso-5,5,7,12,12,14-Hexamethyl-1,4,8,11-tetraazacyclotetradecane)copper(II) bis[O,O′-(o-phenylene)dithiophosphate]." Acta Crystallographica Section E Structure Reports Online 66, no. 12 (2010): m1593. http://dx.doi.org/10.1107/s1600536810046684.

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29

Colucci, W. J., S. J. Jungk, J. W. Nail, et al. "2,2'-[o-Phenylenebis(methyleneoxy)]diacetophenone, C24H22O4." Acta Crystallographica Section C Crystal Structure Communications 41, no. 4 (1985): 554–56. http://dx.doi.org/10.1107/s0108270185004644.

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30

Lu, Kui, Guang-Zhong Tu, Xiang-Feng Guo, et al. "Structure and isomerization of O,O-phenylene penta-coordinated phosphoryl serine." Journal of Molecular Structure 610, no. 1-3 (2002): 65–72. http://dx.doi.org/10.1016/s0022-2860(02)00002-9.

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31

Matsui, H., S. Yamamoto, Y. Izawa, S. Karuppuchamy, and M. Yoshihara. "Electron transfer behavior of calcined material obtained from a samarium-O–phenylene-S–nickel-S–phenylene-O hybrid copolymer." Materials Chemistry and Physics 103, no. 1 (2007): 127–31. http://dx.doi.org/10.1016/j.matchemphys.2007.01.022.

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32

Scheytza, Holger, and Hans-Ulrich Reissig. "Cyclo(paraquat-o-phenylene-paraquat-p-phenylene) — the missing isomeric carbophane of 4,4′-bipyridine." Tetrahedron Letters 39, no. 47 (1998): 8637–40. http://dx.doi.org/10.1016/s0040-4039(98)02039-5.

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33

Peres, L. O., H. Varela, J. R. Garcia, et al. "On the electrochemical polymerization of poly(p-phenylene vinylene) and poly(o-phenylene vinylene)." Synthetic Metals 118, no. 1-3 (2001): 65–70. http://dx.doi.org/10.1016/s0379-6779(00)00282-4.

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34

Stritt, H. P., H. J. Wörz, and H. P. Latscha. "Bildungsmechanismus und Folgereaktionen von 1.2.5.6-Tetraphospha-3.4—7.8-dibenzo-2.6-diiodo-bicycIo[3.3.0]octan Elektrochemische Darstellung von 1.2.5.6-Tetraphospha-3.4—7.8-dibenzo-2.6-dichloro-bicyclo[3.3.0]octan / Formation and Reaction Products of 1.2.5.6-Tetraphospha-3.4—7.8-dibenzo-2.6-diiodo-bicyclo[3.3.0]octane Electrochemical Synthesis of 1.2.5.6-Tetraphospha-3.4—7.8-dibenzo-2.6-diiodo-bicyclo[3.3.0]octane." Zeitschrift für Naturforschung B 40, no. 12 (1985): 1711–14. http://dx.doi.org/10.1515/znb-1985-1218.

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Abstract The reaction of o-phenylene-bis(dichlorophosphane) (1) [2] with anhydrous Lil in benzene gives o-phenylene-bis(diiodophosphane) (2). In the presence of water the reaction leads to the bicyclus 3 [1], Electrolysis of 1 with a mercury-pool at a potential of -800 mV in a 1.2-dichloroethane/ 0.1 Mtetrabutylammonium tetrafluoroborate solution gives 1.2.5.6-tetraphospha- 3.4-7.8-dibenzo-2.6-dichloro-bicyclo[3.3.0]octane (4). The reduction of 3, either by magnesium in THF or by electrolysis in 1.2-DCE/0.1 M TBATFB solution at a potential of -1 V yields the oligomer (o-C6H4P2)5

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35

Du, Hai-Tang, Hai-Jun Du, and Weiyi Zhou. "3,3′-Di-2-naphthoyl-1,1′-(o-phenylene)dithiourea." Acta Crystallographica Section E Structure Reports Online 64, no. 9 (2008): o1780. http://dx.doi.org/10.1107/s1600536808026299.

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36

Xi, Hai-Ling, Jian-Ming Zhang, and Yi-Tao Li. "N,N′-[Methylenedi(3,5-dimethyl-o-phenylene)]diphthalimide." Acta Crystallographica Section E Structure Reports Online 63, no. 10 (2007): o4176. http://dx.doi.org/10.1107/s1600536807046624.

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37

Furukawa, T., H. Matsui, H. Hasegawa, S. Karuppuchamy, and M. Yoshihara. "Electronic behaviours of calcined materials from a (S-nickel-S-phenylene-O)-strontium-(O-phenylene-S-selenium-S) hybrid copolymer." Solid State Communications 142, no. 1-2 (2007): 99–103. http://dx.doi.org/10.1016/j.ssc.2007.01.011.

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38

Habibi, Mohammad Hossein, Morteza Montazerozohori, Reza Mokhtari, Ross W. Harrington, and William Clegg. "3,3′-Dimethoxy-2,2′-[o-phenylenebis(nitrilomethylidyne)]diphenol." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4462. http://dx.doi.org/10.1107/s160053680704826x.

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The title Schiff base compound, C19H20N2O4, was synthesized by the reaction of o-phenylenediamine with 6-methoxysalicylaldehyde. The central benzene ring makes dihedral angles of 2.78 (5) and 73.98 (5)° with the two terminal phenol rings. Each methoxy group is coplanar with the attached phenol ring. The crystal structure is stabilized by intramolecular O—H...N and intermolecular C—H...O hydrogen bonds.

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39

Liu, Yin-Qiu, Xi-Rui Zeng, Qiu-Yan Luo, and Ya-Ping Xu. "{2,2′-[o-Phenylenebis(nitrilomethylidyne)]diphenolato}manganese(II)." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): m2854. http://dx.doi.org/10.1107/s1600536807052993.

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The title complex, [Mn(C20H14N2O2)], is a mononuclear manganese(II) compound. The manganese(II) ion is four-coordinated in a square-planar geometry by two imine N and two phenolate O atoms from one 2,2′-[o-phenylenebis(nitrilomethylidyne)]diphenolate Schiff base ligand. No strong hydrogen bonds were found in the crystal structure.

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40

Liu, Yin-Qiu, Xi-Rui Zeng, Qiu-Yan Luo, and Ya-Ping Xu. "{2,2′-[o-Phenylenebis(nitrilomethylidyne)]diphenolato}zinc(II)." Acta Crystallographica Section E Structure Reports Online 63, no. 9 (2007): m2396. http://dx.doi.org/10.1107/s1600536807040640.

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41

Zhang, Chao-Yan, Qian Gao, Yue Cui, and Ya-Bo Xie. "2,2′-[o-Phenylenebis(methylenethio)]bis(pyridineN-oxide)." Acta Crystallographica Section E Structure Reports Online 65, no. 7 (2009): o1482. http://dx.doi.org/10.1107/s160053680902073x.

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42

Gao, Jing, and Yan Cheng. "2,2′-[5-Bromo-o-phenylenebis(nitrilomethylidyne)]diphenol." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (2009): o979. http://dx.doi.org/10.1107/s1600536809011581.

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43

Aydin, Abdullah, Mehmet Akkurt, Sumeyye Turanli, Deniz Lengerli, Erden Banoglu, and Nefise Dilek Ozcelik. "Crystal structure and Hirshfeld surface analysis of 4-(4-chlorophenyl)-5-methyl-3-{4-[(2-methylphenyl)methoxy]phenyl}-1,2-oxazole." Acta Crystallographica Section E Crystallographic Communications 77, no. 4 (2021): 346–50. http://dx.doi.org/10.1107/s2056989021002383.

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In the title compound, C24H20ClNO2, the mean planes of 4-chlorophenyl, 2-methylphenyl and phenylene rings make dihedral angles of 62.8 (2), 65.1 (3) and 15.1 (2)°, respectively, with the 5-methyl-1,2-oxazole ring. In the crystal, molecules are linked by intermolecular C—H...N, C—H...Cl, C—H...π contacts and π–π stacking interactions between the phenylene groups. Hirshfeld surface analysis indicates that the most important contributions to the crystal packing are from H...H (48.7%), H...C/C...H (22.2%), Cl...H/H...Cl (8.8%), H...O/O...H (8.2%) and H...N/N...H (5.1%) interactions.

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44

Köpf, Hartmut, and Verena Richtering. "Metallocene o-Phenylenebis(phenylphosphido) Chelates of Molybdenum and Tungsten / Metallocene o-Phenylenebis(phenylphosphido) Chelates of Molybdenum and Tungsten." Zeitschrift für Naturforschung B 43, no. 12 (1988): 1653–55. http://dx.doi.org/10.1515/znb-1988-1220.

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Abstract The reaction of the metallocene dichlorides Cp2MCl2 (Cp = η5-C5H5; M = Mo, W) with equimolar amounts of dilithium-o-phenylenebis(phenylphosphide) 1,2-(LiPPh)2C6H4 yields the five-membered chelate complexes Cp2M[1,2-(PPh)2C6H4] (M = Mo. 1; W, 2). Compounds 1 and 2 are characterized by IR, NMR and mass spectra

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45

Slutsky, Morris M., Jason S. Phillip, and Gregory N. Tew. "Synthesis and characterization of amphiphilic o-phenylene ethynylene oligomers." New Journal of Chemistry 32, no. 4 (2008): 670. http://dx.doi.org/10.1039/b707618e.

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46

Liu, Yin-Qiu, та Xi-Rui Zeng. "[N,N′-(o-Phenylene)dipicolinamide-κ4 N]nickel(II)". Acta Crystallographica Section E Structure Reports Online 63, № 11 (2007): m2684. http://dx.doi.org/10.1107/s1600536807048386.

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The title compound, [Ni(C18H12N4O2)], which was synthesized by reaction of N-[2-(picolinamido)phenyl]picolinamide with Ni(NO3)2·6H2O in ethanol, is a mononuclear complex in which the nickel(II) ion is coordinated by four N atoms and displays a distorted square-planar coordination geometry.

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47

Coseri, Sergiu, and Adrian Caraculacu. "1,2-Ethylene-bis(o-N2-phenylene-N1,N1-dimethylformamidine)." Molecules 5, no. 12 (2000): M166. http://dx.doi.org/10.3390/m166.

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48

Slutsky, Morris M., Ticora V. Jones, and Gregory N. Tew. "Spin System Assignment of Homo-o-Phenylene Ethynylene Oligomers." Journal of Organic Chemistry 72, no. 2 (2007): 342–47. http://dx.doi.org/10.1021/jo061175f.

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49

Li, Xue-Mei, Li-Ping Du, and Shu-Sheng Zhang. "3,3′-Dimethyl-2,2′-dinitro-N,N′-(o-phenylene)dibenzamide." Acta Crystallographica Section E Structure Reports Online 62, no. 6 (2006): o2535—o2536. http://dx.doi.org/10.1107/s1600536806019076.

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50

Azev, Yu A., E. O. Sidorov, and I. I. Hudretsova. "Reaction op phervenulin-3-one with o-phenylene diamines." Chemistry of Heterocyclic Compounds 21, no. 12 (1985): 1396. http://dx.doi.org/10.1007/bf00842972.

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