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Relevant bibliographies by topics / Phenylene Compounds

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Academic literature on the topic 'Phenylene Compounds'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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Journal articles on the topic "Phenylene Compounds"

1

Vogel, Sabine, Gottfried Huttner, and Laszlo Zsolnai. "Fünffach koordinierte Co(III)-Komplexe [Tripod-Cobalt-(ortho(X)(Y)C6H4)]+ mit ortho-phenylenverbrückten Chelatliganden [(XH)(YH)C6H4] (XH, YH = NH2, OH, SH) / Five-Coordinate Co(III) Complexes [Tripod-Cobalt-(ortho-(X)(Y)C6H4)]+ Containing ortho-Phenylene-Bridged Chelate Ligands [(XH)(YH)C6H4] (XH, YH = NH2, OH, SH)." Zeitschrift für Naturforschung B 48, no. 5 (1993): 641–52. http://dx.doi.org/10.1515/znb-1993-0514.

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The ortho-phenylene compounds ortho-[(XH)(YH)C6H4] (XH, YH = NH2, SH, OH) react with Co(BF4)2•6H2O and Tripod (CH3C(CH2PPh2)3) to give the five-coordinate Co(III) complexes [Tripod-Cobalt-(ortho-(X)(Y)C6H4)]+ (X, Y = NH, O, S), 1-6.The structures of 1—6 have been characterized by X-ray analyses of appropriate salts. The compounds have further been characterized by IR, NMR, UV-VIS and cyclovoltammetric measurements.As a compound analogous to 1—6, but containing the saturated chelate ligand [(S)C2H4(S)]2- instead of the conjugated ortho-phenylene type ligands of 1-6, [Tripod-Cobalt-((S)C2H4(S))]

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2

Caldera Villalobos, Martín, Jesús García Serrano, and Ana María Herrera González. "Synthesis, Characterization and Mesomorphic Properties of N,N'-(1,4-Phenylene(methanylylidene))bis(4-(hexyloxy)aniline)." Advanced Materials Research 976 (June 2014): 75–79. http://dx.doi.org/10.4028/www.scientific.net/amr.976.75.

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Liquid crystals (LCs) are compounds that have properties between isotropic liquids and solid crystal materials. Although there is not a parameter to predict this behavior, the liquid crystals reported until now have common characteristics, for example rigid groups such as columns or rods within its structures, and long hydrocarbon chains that give flexibility. In this work we report the synthesis and characterization of LCN,N'-(1,4-phenylene bis (methanylylidene)) bis (4-(hexyloxy) aniline). The compound was characterized by infrared (IR), raman and1H-nuclear magnetic resonance (1H-NMR) spectr

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3

Sivakumar*, Kuttiyapillai, and Dr Venkatachalam Chandrasekaran. "Trinuclear Schiff Base Complexes Containing P-Phenylene Diamine, 2, 3-Pentanedione and 3-Aminocoumarin Ligand: Synthesis, Characterization, DNA Cleavage and Antimicrobial Activity." International Journal of Innovative Technology and Exploring Engineering 9, no. 5 (2020): 2283–92. http://dx.doi.org/10.35940/ijitee.e2498.039520.

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Trinuclear Schiff base complexes were synthesized by using p-phenylene diamine, 2,3-pentanedione and 3-aminocoumarin and Cu (II), Ni (II), Mn (II), Zn(II) and Cr(III) chloride salts. The category of compound was [M3LCl6]. All trinuclear compounds were analyzed by C, H&N analysis and spectral studies. Mechanism of thermal analysis of trinuclear Schiff base metal complexes was studied. The electrophoresis data confirmed that Schiff base compounds cleaved DNA with Hydrogen peroxide. Additionally, the antibacterial action was tested by disc diffusion method. The efficiency of compounds was ass

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4

Mehenni, Hakim, Hélène Guillou, Christian Tessier, and Josée Brisson. "Effect of chain ends on the structure of aramid oligomers." Canadian Journal of Chemistry 86, no. 1 (2008): 7–19. http://dx.doi.org/10.1139/v07-132.

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Synthesis, X-ray diffraction, and Fourier transform infrared spectroscopy of aliphatic–aromatic aramid oligomers are reported with the aim of shedding light on the effect of end-chain substituent on the morphology and structure of poly(para-phenylene terephthalamide) or PPTA. Three types of X-ray powder diffraction patterns were observed: one similar to that of PPTA form I, one similar to that of PPTA form II, and an additional form never reported. Some compounds, differing by their internal distribution of amide–aromatic rings, adopt two different crystal structures, whereas compounds having

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5

Chantrell, P. G., C. A. Pearce, C. R. Toyer, and R. Twaits. "Preparation of some novel diphosphorus compounds. I. 1,4-phenylene-diphosphorus compounds." Journal of Applied Chemistry 14, no. 12 (2007): 563–64. http://dx.doi.org/10.1002/jctb.5010141206.

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6

Matsuo, Takumi, Carina Rössiger, Jasmin Herr, et al. "Synthesis and characterization of methoxy- or cyano-substituted thiophene/phenylene co-oligomers for lasing application." RSC Advances 10, no. 40 (2020): 24057–62. http://dx.doi.org/10.1039/d0ra04742b.

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7

Jabar, Maha A., and Nisreen H. Karam. "Synthesis and characterization of azo liquid crystal compounds based on 5H-Thiazolo [3,4-b][1,3,4]thiadiazole unit." Bionatura 7, no. 2 (2022): 1–4. http://dx.doi.org/10.21931/rb/2022.07.02.17.

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A calamitic symmetric liquid crystalline consisting of an azo group containing 5H-Thiazolo[3,4-b][1,3,4]thiadiazole moiety compound[III] was synthesized via sequence reactions starting from reaction terephthaldehyde with mercaptoacetic acid and thiosemicarbazide in the presence of concentrated sulfuric acid to synthesized 5,5'-(1,4-phenylene)bis(5H-thiazolo[4,3-b][1,3,4]thiadiazol-2-amine)[I] then the azo compound [II] synthesized by coupling between diazonium salt of the compound [I] with phenol at(0-4) ̊C., after that the compound [III] was synthesized by the reaction of the compound [II] wi

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8

Shaker, Raafat M. "Synthesis of 1,4-phenylene bridged bis-heterocyclic compounds." Arkivoc 2012, no. 1 (2011): 1–44. http://dx.doi.org/10.3998/ark.5550190.0013.101.

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9

Betz, Richard, and Peter Klüfers. "1-(Ylomethyl)cyclopentyl 1′,2′-phenylene orthocarbonate." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4300. http://dx.doi.org/10.1107/s1600536807049434.

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The dispiro title compound (systematic name: 1,4,6,13-tetraoxa-2,3-benzodispiro[4.1.4.2]tridecane), C13H14O4, is an asymmetric orthocarbonic acid ester of an aromatic and an aliphatic vicinal diol. C—O bond lengths at the orthoester centre show a typical difference of about 0.06 Å, as has been observed for related spiro esters with an aliphatic component that does not impose steric strain in the vicinity of the orthocarbonic acid centre. The C—O bond-length differences are also observed in density functional theory (DFT) calculations, thus ruling out a decisive influence of intermolecular forc

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10

Dong, Hui, Li Wang, Meng Guo, et al. "Antioxidant and Anticancer Activities of Synthesized Methylated and Acetylated Derivatives of Natural Bromophenols." Antioxidants 11, no. 4 (2022): 786. http://dx.doi.org/10.3390/antiox11040786.

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Natural bromophenols are important secondary metabolites in marine algae. Derivatives of these bromophenol are potential candidates for the drug development due to their biological activities, such as antioxidant, anticancer, anti-diabetic and anti-inflammatory activity. In our present study, we have designed and synthesized a series of new methylated and acetylated bromophenol derivatives from easily available materials using simple operation procedures and evaluated their antioxidant and anticancer activities on the cellular level. The results showed that 2.,3-dibromo-1-(((2-bromo-4,5-dimeth

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Dissertations / Theses on the topic "Phenylene Compounds"

1

De, Souza Melanie Maria. "Photophysical studies of chromophores in conjugated polymers and model compounds based on para-phenylene vinylene." Thesis, Imperial College London, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.394385.

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2

Cai, Qingrui. "Temperature and pressure raman studies of Hg1201 superconductors and oligo (para-phenylene) materials /." free to MU campus, to others for purchase, 2001. http://wwwlib.umi.com/cr/mo/fullcit?p3025607.

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3

Som, Abhijit. "Linear And Hyperbranched Polybenzyls And Poly(Meta-Phenylenes)." Thesis, 2004. https://etd.iisc.ac.in/handle/2005/1220.

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Som, Abhijit. "Linear And Hyperbranched Polybenzyls And Poly(Meta-Phenylenes)." Thesis, 2004. http://etd.iisc.ernet.in/handle/2005/1220.

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5

"The synthesis of [n]paracyclophane-based chiral non-racemic oligo[p-phenylene-(E)-vinylene]s." 2000. http://library.cuhk.edu.hk/record=b6073298.

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Wei Chunmei.<br>"September 2000."<br>Thesis (Ph.D.)--Chinese University of Hong Kong, 2000.<br>Includes bibliographical references (p. 137-140).<br>Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.<br>Mode of access: World Wide Web.<br>Abstracts in English and Chinese.

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6

Anusooya, Y. "Properties Of The Correlated Electronic States In Conjugated Organic Molecules, Polymers And Metal-Halogen Chains." Thesis, 1996. https://etd.iisc.ac.in/handle/2005/1943.

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Anusooya, Y. "Properties Of The Correlated Electronic States In Conjugated Organic Molecules, Polymers And Metal-Halogen Chains." Thesis, 1996. http://etd.iisc.ernet.in/handle/2005/1943.

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8

Liu, Yanbing. "I. The design and synthesis of model compounds for study of high -spin organic magnetic materials. II. The design and synthesis of soluble and regioregular poly(phenylene vinylene)s." 2000. https://scholarworks.umass.edu/dissertations/AAI9960766.

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Various model radicals were synthesized and studied for their spin coupling by ESR spectroscopy. Diphenoxyl radical 7 is an indirect spin coupling model with long range conjugation. Diphenoxyl radical 12 is a direct coupling model with shorter conjugation. The ESR spectra of the both diradicals were studied to understand their spin interactions. In order to understand spin delocalization further in these radical systems, two other model compounds with simpler structure, 14 and 15, were designed and synthesized, and their ESR spectra studied. An interesting ESR spectrum was obtained for a diaci

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Books on the topic "Phenylene Compounds"

1

Li, Yiting. Synthesis and photophysics of mono-disperse phenylene ethynylene oligomers that feature Ru(II), Os(II), and Re(l) polypyridine complexes. 2001.

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Book chapters on the topic "Phenylene Compounds"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of manganese(III) N, N′-(o-phenylene) bis- (salicylideneimine)selenocyanate complex." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49202-4_618.

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2

Osawa, Z., S. Kuroda, S. Kobayashi, and F. Tanabe. "Photodegradation Mechanisms of Poly(p-phenylene sulfide) and Its Model Compounds." In Advances in Chemistry. American Chemical Society, 1996. http://dx.doi.org/10.1021/ba-1996-0249.ch009.

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3

Pardasani, R. T., and P. Pardasani. "Magnetic properties of heterotetranuclear Cu3Co complex with N,N′-o-phenylene-bis(3-ethoxysalicylaldimine)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_479.

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4

Pardasani, R. T., and P. Pardasani. "Magnetic properties of heterotetranuclear Cu3Mn complex with N,N′-o-phenylene-bis(3-ethoxysalicylaldimine)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 8. Springer Berlin Heidelberg, 2023. http://dx.doi.org/10.1007/978-3-662-66460-5_478.

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5

Pardasani, R. T., and P. Pardasani. "Magnetic properties of cobalt(II) complex with N,N′-(dithiodiethylenebis- (aminylydenemethylene)-bis(1,2-phenylene)ditosylamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_195.

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6

Pardasani, R. T., and P. Pardasani. "Magnetic properties of iron(II) complex with N,N′-(dithiodiethylenebis- (aminylydenemethylene)-bis(1,2-phenylene)ditosylamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_89.

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7

Pardasani, R. T., and P. Pardasani. "Magnetic properties of copper(II) complex with N,N′-(dithiodiethylenebis- (aminylydenemethylene)-bis(1,2-phenylene)ditosylamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_377.

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8

Pardasani, R. T., and P. Pardasani. "Magnetic properties of polymeric cobalt(II) complex with 1,3-phenylene-diacetate ad 4,4′-bipyridine ligands." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_199.

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9

Pardasani, R. T., and P. Pardasani. "Magnetic properties of nickel(II) complex with N,N′-(dithiodiethylenebis- (aminylydenemethylene)-bis(1,2-phenylene)ditosylamide." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_258.

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10

Pardasani, R. T., and P. Pardasani. "Magnetic properties of phenylene-bridged dinuclear nickel(II) chloro complex with 16-membered pentaaza macrocyclic ligand." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 5. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65098-1_329.

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Conference papers on the topic "Phenylene Compounds"

1

Paiva, Laura Simonassi Raso de, Leonardo Evaristo de Sousa, and Pedro Henrique de Oliveira Neto. "Energy transport in conjugated polymers: electronic structure and kinetic Monte Carlo simulations." In VIII Simpósio de Estrutura Eletrônica e Dinâmica Molecular. Universidade de Brasília, 2020. http://dx.doi.org/10.21826/viiiseedmol202076.

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Conjugated polymers are materials that have attracted much attention from the research community because of their charge and energy transport properties. In this sense, it is necessary to understand the mechanism behind exciton transfer in this particular class of systems. However, direct application of procedures done for different organic compounds is not straightforward for long polymeric chains, because such procedures would be computationally impracticable. In that matter, alternative treatments are required. In this work, we perform spectrum simulations for poly-thiophene (PTH) and poly(

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