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Journal articles on the topic 'Benzoquinonemonoimine'

Author: Grafiati

Published: 25 May 2024

Last updated: 31 July 2025

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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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11

Das, Dipanwita, Hemlata Agarwala, Abhishek Dutta Chowdhury, et al. "Four-Center Oxidation State Combinations and Near-Infrared Absorption in [Ru(pap)(Q)2]n(Q=3,5-Di-tert-butyl-N-aryl-1,2-benzoquinonemonoimine, pap=2-Phenylazopyridine)." Chemistry - A European Journal 19, no. 23 (2013): 7384–94. http://dx.doi.org/10.1002/chem.201204620.

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12

Kauf, Thomas, Vitor Rosa, Christophe Fliedel, et al. "Reactivity of TCNE and TCNQ derivatives of quinonoid zwitterions with Cu(i)." Dalton Transactions 44, no. 12 (2015): 5441–50. http://dx.doi.org/10.1039/c4dt03956d.

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13

Touil, Mounia, Mohammed Lachkar, and Olivier Siri. "New sterically unhindered benzoquinonemonoimines." Tetrahedron Letters 52, no. 28 (2011): 3678–80. http://dx.doi.org/10.1016/j.tetlet.2011.05.035.

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14

Konovalova, S. A., A. P. Avdeenko, V. V. Pirozhenko, and G. O. Santalova. "Conformational transformations of N-[arylsulfonylimino(methyl)methyl]-1,4-benzoquinonemonoimines." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 5 (November 2024): 4–11. http://dx.doi.org/10.32434/0321-4095-2024-156-5-4-11.

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In solutions of N-[arylsulfonylimino(methyl)methyl]-1,4-benzoquinonemonoimines, several Z,E-isomerization processes occur simultaneously: a fast inversion isomerization process (topomerization) relative to the C=N1 quinoneimine bond; a slow inversion isomerization process relative to the C=N2 exocyclic bond; and a process of inhibited rotation around the =N1–С= bond that connects two imine fragments. In the 1H NMR spectra, isomerization with respect to the C=N2 exocyclic bond was only detected. The theoretical values of the isomerization barriers for the C=N1 and C=N2 bonds, as well as for the

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15

Burmistrov, K. S., N. V. Toropin, V. I. Galamai, et al. "ChemInform Abstract: Reactions of N-Aryl-1,4-benzoquinonemonoimines with 2,5-Bis(arylamino)-N-aryl-1,4-benzoquinonemonoimines." ChemInform 31, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.200013043.

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16

Das, Dipanwita, Tapan Kumar Mondal, Shaikh M. Mobin, and Goutam Kumar Lahiri. "Sensitive Valence Structures of [(pap)2Ru(Q)]n(n= +2, +1, 0, −1, −2) with Two Different Redox Noninnocent Ligands, Q = 3,5-Di-tert-butyl-N-aryl-1,2-benzoquinonemonoimine and pap = 2-Phenylazopyridine†." Inorganic Chemistry 48, no. 20 (2009): 9800–9810. http://dx.doi.org/10.1021/ic901343j.

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17

Ye, Shengfa, Biprajit Sarkar, Carole Duboc, Jan Fiedler, and Wolfgang Kaim. "The Redox Series [M(bpy)2(Q)]n+, M = Ru or Os, Q = 3,5-Di-tert-butyl-N-phenyl-1,2-benzoquinonemonoimine. Isolation and a Complete X and W Band EPR Study of the Semiquinone States (n= 1)." Inorganic Chemistry 44, no. 8 (2005): 2843–47. http://dx.doi.org/10.1021/ic048407i.

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18

Avdeenko, Anatoly P., Vladimir V. Pirozhenko, Svetlana A. Konovalova, Anna A. Santalova, and Anatoliy V. Vakulenko. "Synthesis and structure investigations of N-arylsulfinyl-1,4-benzoquinonemonoimines." Arkivoc 2005, no. 8 (2005): 60–71. http://dx.doi.org/10.3998/ark.5550190.0006.805.

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19

Konovalova, S. A., A. P. Avdeenko, V. V. Pirozhenko, and S. A. Goncharova. "Conformational transformation of N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinonemonoimines." Voprosy Khimii i Khimicheskoi Tekhnologii, no. 2 (May 2023): 75–81. http://dx.doi.org/10.32434/0321-4095-2023-147-2-75-81.

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It was established that in the solutions of N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinonemonoimines there are both Z,E-isomerization relative to C=N bonds and atropoisomerism (inhibited rotation around the =N1–C= bond). The latter can be detected when there are the diastereotopic isopropyl groups in the quinoid ring. The rate constants of this process were calculated by the method of analysis of the full line in the 1H NMR spectra. Activation thermodynamic parameters were determined on their basis. With the help of quantum-chemical calculations, we proved that the determined experimenta

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20

BURMISTROV, K. S., N. V. TOROPIN, and S. I. BURMISTROV. "ChemInform Abstract: Reactions of Hydrogen Bromide with N-Aryl-1,4-benzoquinonemonoimines." ChemInform 25, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199418063.

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21

AVDEENKO, A. P., and N. V. VELICHKO. "ChemInform Abstract: Reaction of N-Arylsulfonyl-1,4-benzoquinonemonoimines with Hydrogen Chloride in DMF." ChemInform 25, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199418062.

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22

AFANASY'EVA, G. B., and E. V. TZOI. "ChemInform Abstract: Studies of Heterocyclic Quinonimines. Part 11. Influence of Benzanellation on the Oxidative Cyclization of Diarylamino-N-aryl-1,4- benzoquinonemonoimines into Phenazinone Derivatives." ChemInform 24, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199302207.

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23

Konovalova, S. A., A. P. Avdeenko, and O. N. Lysenko. "Cycloaddition of 2,3-dimethyl-1,3-butadiene to 1,4-benzoquinonemonoimine derivatives." Kharkov University Bulletin Chemical Series, 2017. http://dx.doi.org/10.26565/2220-637x-2017-28-10.

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24

Rosa, Luis G., Julian Velev, Zhengzheng Zhang, et al. "Back Cover: Approaching an organic semimetal: Electron pockets at the Fermi level for a p -benzoquinonemonoimine zwitterion (Phys. Status Solidi B 8/2012)." physica status solidi (b) 249, no. 8 (2012). http://dx.doi.org/10.1002/pssb.201290020.

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