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Articoli di riviste sul tema "Benzoquinonemonoimine"

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Autore: Grafiati
Pubblicato: 25 maggio 2024

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1

Dowben, Peter A., Donna A. Kunkel, Axel Enders, Luis G. Rosa, Lucie Routaboul, Bernard Doudin e Pierre Braunstein. "The Dipole Mediated Surface Chemistry of p-Benzoquinonemonoimine Zwitterions". Topics in Catalysis 56, n. 12 (18 giugno 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 e Pierre Braunstein. "ChemInform Abstract: The Dipole Mediated Surface Chemistry of P-Benzoquinonemonoimine Zwitterions". ChemInform 44, n. 39 (5 settembre 2013): no. http://dx.doi.org/10.1002/chin.201339257.

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3

BURMISTROV, K. S., N. V. TOROPIN, S. I. BURMISTROV e V. M. NICHVOLODA. "ChemInform Abstract: Reaction of N-(p-Tolyl)-1,4-benzoquinonemonoimine with Thiocyanic Acid." ChemInform 24, n. 42 (20 agosto 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 e Olivier Siri. "The Quinonoid Zwitterion Interlayer for the Improvement of Charge Carrier Mobility in Organic Field-Effect Transistors". Polymers 13, n. 10 (13 maggio 2021): 1567. http://dx.doi.org/10.3390/polym13101567.

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Abstract (sommario):
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, n. 8 (22 marzo 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 e Pierre Braunstein. "Nickel Complexes with Functional ZwitterionicN,O-Benzoquinonemonoimine-Type Ligands: Syntheses, Structures, and Catalytic Oligomerization of Ethylene". Organometallics 25, n. 23 (novembre 2006): 5518–27. http://dx.doi.org/10.1021/om060600s.

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7

Kauf, Thomas, e Pierre Braunstein. "Contrasting behaviour of TCNE and TCNQ zwitterionic benzoquinonemonoimine derivatives and coordination of a tricyanoethenyl substituent to Pd(0)". Dalton Transactions 40, n. 39 (2011): 9967. http://dx.doi.org/10.1039/c1dt10804b.

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8

Antonov, A. V., e 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, n. 5 (maggio 2007): 883–89. http://dx.doi.org/10.1007/s11172-007-0133-x.

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9

Yang, Qing-Zheng, Olivier Siri e 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, n. 24 (9 dicembre 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 e 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, n. 33 (2011): 8377. http://dx.doi.org/10.1039/c1dt10609k.

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11

Kauf, Thomas, Vitor Rosa, Christophe Fliedel, Roberto Pattacini, Naina Deibel, Teresa Avilés, Biprajit Sarkar e Pierre Braunstein. "Reactivity of TCNE and TCNQ derivatives of quinonoid zwitterions with Cu(i)". Dalton Transactions 44, n. 12 (2015): 5441–50. http://dx.doi.org/10.1039/c4dt03956d.

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12

Das, Dipanwita, Hemlata Agarwala, Abhishek Dutta Chowdhury, Tuhin Patra, Shaikh M. Mobin, Biprajit Sarkar, Wolfgang Kaim e Goutam Kumar Lahiri. "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, n. 23 (9 aprile 2013): 7384–94. http://dx.doi.org/10.1002/chem.201204620.

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13

Touil, Mounia, Mohammed Lachkar e Olivier Siri. "New sterically unhindered benzoquinonemonoimines". Tetrahedron Letters 52, n. 28 (luglio 2011): 3678–80. http://dx.doi.org/10.1016/j.tetlet.2011.05.035.

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14

Burmistrov, K. S., N. V. Toropin, V. I. Galamai, W. Likussar, A. Michelitsch, M. Wurglics e M. Schubert-Zsilavecz. "ChemInform Abstract: Reactions of N-Aryl-1,4-benzoquinonemonoimines with 2,5-Bis(arylamino)-N-aryl-1,4-benzoquinonemonoimines." ChemInform 31, n. 13 (9 giugno 2010): no. http://dx.doi.org/10.1002/chin.200013043.

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15

Das, Dipanwita, Tapan Kumar Mondal, Shaikh M. Mobin e 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, n. 20 (19 ottobre 2009): 9800–9810. http://dx.doi.org/10.1021/ic901343j.

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16

Ye, Shengfa, Biprajit Sarkar, Carole Duboc, Jan Fiedler e 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, n. 8 (aprile 2005): 2843–47. http://dx.doi.org/10.1021/ic048407i.

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17

Konovalova, S. A., A. P. Avdeenko, V. V. Pirozhenko e S. A. Goncharova. "Conformational transformation of N-[arylsulfonylimino(phenyl)methyl]-1,4-benzoquinonemonoimines". Voprosy Khimii i Khimicheskoi Tekhnologii, n. 2 (maggio 2023): 75–81. http://dx.doi.org/10.32434/0321-4095-2023-147-2-75-81.

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Abstract (sommario):
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 experimental barriers corresponded exactly to the inhibited rotation around the bond =N1–C=.
18

Avdeenko, Anatoly P., Vladimir V. Pirozhenko, Svetlana A. Konovalova, Anna A. Santalova e Anatoliy V. Vakulenko. "Synthesis and structure investigations of N-arylsulfinyl-1,4-benzoquinonemonoimines". Arkivoc 2005, n. 8 (19 novembre 2005): 60–71. http://dx.doi.org/10.3998/ark.5550190.0006.805.

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19

BURMISTROV, K. S., N. V. TOROPIN e S. I. BURMISTROV. "ChemInform Abstract: Reactions of Hydrogen Bromide with N-Aryl-1,4-benzoquinonemonoimines." ChemInform 25, n. 18 (19 agosto 2010): no. http://dx.doi.org/10.1002/chin.199418063.

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20

AVDEENKO, A. P., e N. V. VELICHKO. "ChemInform Abstract: Reaction of N-Arylsulfonyl-1,4-benzoquinonemonoimines with Hydrogen Chloride in DMF." ChemInform 25, n. 18 (19 agosto 2010): no. http://dx.doi.org/10.1002/chin.199418062.

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21

AFANASY'EVA, G. B., e 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, n. 2 (21 agosto 2010): no. http://dx.doi.org/10.1002/chin.199302207.

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22

Konovalova, S. A., A. P. Avdeenko e 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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23

Rosa, Luis G., Julian Velev, Zhengzheng Zhang, Jose Alvira, Omar Vega, Gerson Diaz, Lucie Routaboul 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, n. 8 (agosto 2012). http://dx.doi.org/10.1002/pssb.201290020.

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