Relevant bibliographies by topics / Benzoquinonemonoimine

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Benzoquinonemonoimine'

Author: Grafiati
Published: 25 May 2024
Last updated: 31 July 2025

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Journal articles on the topic "Benzoquinonemonoimine"

1

Dowben, Peter A., Donna A. Kunkel, Axel Enders, et al. "The Dipole Mediated Surface Chemistry of p-Benzoquinonemonoimine Zwitterions." Topics in Catalysis 56, no. 12 (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, et al. "ChemInform Abstract: The Dipole Mediated Surface Chemistry of P-Benzoquinonemonoimine Zwitterions." ChemInform 44, no. 39 (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 (2010): no. http://dx.doi.org/10.1002/chin.199342146.

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4

Luczak, Adam, Angélina Torres Ruiz, Simon Pascal, et al. "The Quinonoid Zwitterion Interlayer for the Improvement of Charge Carrier Mobility in Organic Field-Effect Transistors." Polymers 13, no. 10 (2021): 1567. http://dx.doi.org/10.3390/polym13101567.

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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
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5

Rosa, Luis G., Julian Velev, Zhengzheng Zhang, et al. "Approaching an organic semimetal: Electron pockets at the Fermi level for a p-benzoquinonemonoimine zwitterion." physica status solidi (b) 249, no. 8 (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 (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 (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 (2005): 7237–46. http://dx.doi.org/10.1002/chem.200500704.

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10

Das, Dipanwita, Tapan Kumar Mondal, Abhishek Dutta Chowdhury, et al. "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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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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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 stabl
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Journal articles
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