Relevant bibliographies by topics / Benzoquinonemonoimine

Academic literature on the topic 'Benzoquinonemonoimine'

Author: Grafiati
Published: 25 May 2024

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Contents

  1. Journal articles
  2. Dissertations / Theses

Journal articles on the topic "Benzoquinonemonoimine":

1

Dowben, Peter A., Donna A. Kunkel, Axel Enders, Luis G. Rosa, Lucie Routaboul, Bernard Doudin, and Pierre Braunstein. "The Dipole Mediated Surface Chemistry of p-Benzoquinonemonoimine Zwitterions." Topics in Catalysis 56, no. 12 (June 18, 2013): 1096–103. http://dx.doi.org/10.1007/s11244-013-0075-5.

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2

Dowben, Peter A., Donna A. Kunkel, Axel Enders, Luis G. Rosa, Lucie Routaboul, Bernard Doudin, and Pierre Braunstein. "ChemInform Abstract: The Dipole Mediated Surface Chemistry of P-Benzoquinonemonoimine Zwitterions." ChemInform 44, no. 39 (September 5, 2013): no. http://dx.doi.org/10.1002/chin.201339257.

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3

BURMISTROV, K. S., N. V. TOROPIN, S. I. BURMISTROV, and V. M. NICHVOLODA. "ChemInform Abstract: Reaction of N-(p-Tolyl)-1,4-benzoquinonemonoimine with Thiocyanic Acid." ChemInform 24, no. 42 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199342146.

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4

Luczak, Adam, Angélina Torres Ruiz, Simon Pascal, Adrian Adamski, Jarosław Jung, Beata Luszczynska, and Olivier Siri. "The Quinonoid Zwitterion Interlayer for the Improvement of Charge Carrier Mobility in Organic Field-Effect Transistors." Polymers 13, no. 10 (May 13, 2021): 1567. http://dx.doi.org/10.3390/polym13101567.

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Abstract:
The interface between the semiconductor and the dielectric layer plays a crucial role in organic field-effect transistors (OFETs) because it is at the interface that charge carriers are accumulated and transported. In this study, four zwitterionic benzoquinonemonoimine dyes featuring alkyl and aryl N-substituents were used to cover the dielectric layers in OFET structures. The best interlayer material, containing aliphatic side groups, increased charge carrier mobility in the measured systems. This improvement can be explained by the reduction in the number of the charge carrier trapping sites at the dielectric active layer interface from 1014 eV−1 cm−2 to 2 × 1013 eV−1 cm−2. The density of the traps was one order of magnitude lower compared to the unmodified transistors. This resulted in an increase in charge carrier mobility in the tested poly [2,5-(2-octyldodecyl)-3,6-diketopyrrolopyrrole-alt-5,5-(2,5-di(thien-2-yl)thieno [3,2-b]thiophene)] (DPPDTT)-based transistors to 5.4 × 10−1 cm2 V−1 s−1.
5

Rosa, Luis G., Julian Velev, Zhengzheng Zhang, Jose Alvira, Omar Vega, Gerson Diaz, Lucie Routaboul, et al. "Approaching an organic semimetal: Electron pockets at the Fermi level for a p-benzoquinonemonoimine zwitterion." physica status solidi (b) 249, no. 8 (March 22, 2012): 1571–76. http://dx.doi.org/10.1002/pssb.201147426.

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6

Yang, Qing-Zheng, Anthony Kermagoret, Magno Agostinho, Olivier Siri, and Pierre Braunstein. "Nickel Complexes with Functional ZwitterionicN,O-Benzoquinonemonoimine-Type Ligands: Syntheses, Structures, and Catalytic Oligomerization of Ethylene." Organometallics 25, no. 23 (November 2006): 5518–27. http://dx.doi.org/10.1021/om060600s.

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7

Kauf, Thomas, and Pierre Braunstein. "Contrasting behaviour of TCNE and TCNQ zwitterionic benzoquinonemonoimine derivatives and coordination of a tricyanoethenyl substituent to Pd(0)." Dalton Transactions 40, no. 39 (2011): 9967. http://dx.doi.org/10.1039/c1dt10804b.

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8

Antonov, A. V., and V. T. Varlamov. "Rate constants of elementary steps of the reversible chain reaction of N-phenyl-1,4-benzoquinonemonoimine with 2,5-dichlorohydroquinone." Russian Chemical Bulletin 56, no. 5 (May 2007): 883–89. http://dx.doi.org/10.1007/s11172-007-0133-x.

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9

Yang, Qing-Zheng, Olivier Siri, and Pierre Braunstein. "Tunable N-substitution in Zwitterionic Benzoquinonemonoimine Derivatives: Metal Coordination, Tandemlike Synthesis of Zwitterionic Metal Complexes, and Supramolecular Structures." Chemistry - A European Journal 11, no. 24 (December 9, 2005): 7237–46. http://dx.doi.org/10.1002/chem.200500704.

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10

Das, Dipanwita, Tapan Kumar Mondal, Abhishek Dutta Chowdhury, Fritz Weisser, David Schweinfurth, Biprajit Sarkar, Shaikh M. Mobin, Francisco A. Urbanos, Reyes Jiménez-Aparicio, and Goutam Kumar Lahiri. "Valence and spin situations in isomeric [(bpy)Ru(Q′)2]n (Q′ = 3,5-di-tert-butyl-N-aryl-1,2-benzoquinonemonoimine). An experimental and DFT analysis." Dalton Transactions 40, no. 33 (2011): 8377. http://dx.doi.org/10.1039/c1dt10609k.

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Journal articles

Dissertations / Theses on the topic "Benzoquinonemonoimine":

1

Torres, Ruiz Angelina. "Vers de nouveaux détecteurs des ions cyanures." Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0587.

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Abstract:
Le cyanure étant un des agents les plus toxiques sur notre planète, il est crucial de le détecter avec précision surtout dans l’industrie alimentaire. Les travaux présentés dans cette thèse portent sur le développement de nouveaux détecteurs colorimétriques du cyanure. Dans un premier temps des benzoquinonemonoimines ont été synthétisées et leurs propriétés optiques investiguées (en version ligand libre et complexes). Nous nous sommes ensuite intéressés à la synthèse de macrocycles de type azacalixarènes, dont l’ajout de cyanure en solution permet l’obtention de complexes de Meisenheimer stables. Le travail s’est ensuite focalisé sur la synthèse de dérivés m-dinitro-benzènes comportant différents groupements donneurs et accepteurs dont leurs propriétés optiques ont été étudiées pour la détection colorimétrique du cyanure. Dans une dernière partie, nous avons étudié la teneur en cyanure des Calissons d’Aix
As cyanide is one of the most toxic agents on our planet, it is crucial to detect it accurately, especially in the food industry. The work presented in this thesis concerns the development of new colorimetric cyanide detectors. First, benzoquinonemonoimines were synthesized and their optical properties investigated (in free ligand and complex version). We then focused on the synthesis of azacalixarene-type macrocycles, for which the addition of cyanide in solution gives stable Meisenheimer complexes. The work then focused on the synthesis of m-dinitro-benzenes derivatives incorporating different donor and acceptor groups whose optical properties were studied for the colorimetric detection of cyanide. In the last part, we investigated the cyanide content of Calissons d´Aix

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