Literatura científica selecionada sobre o tema "Benzoquinonemonoimine"
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Artigos de revistas sobre o assunto "Benzoquinonemonoimine"
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.º 12 (18 de junho de 2013): 1096–103. http://dx.doi.org/10.1007/s11244-013-0075-5.
Texto completo da fonteDowben, 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.º 39 (5 de setembro de 2013): no. http://dx.doi.org/10.1002/chin.201339257.
Texto completo da fonteBURMISTROV, 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.º 42 (20 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199342146.
Texto completo da fonteLuczak, 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.º 10 (13 de maio de 2021): 1567. http://dx.doi.org/10.3390/polym13101567.
Texto completo da fonteRosa, 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.º 8 (22 de março de 2012): 1571–76. http://dx.doi.org/10.1002/pssb.201147426.
Texto completo da fonteYang, 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.º 23 (novembro de 2006): 5518–27. http://dx.doi.org/10.1021/om060600s.
Texto completo da fonteKauf, 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.º 39 (2011): 9967. http://dx.doi.org/10.1039/c1dt10804b.
Texto completo da fonteAntonov, 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.º 5 (maio de 2007): 883–89. http://dx.doi.org/10.1007/s11172-007-0133-x.
Texto completo da fonteYang, 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.º 24 (9 de dezembro de 2005): 7237–46. http://dx.doi.org/10.1002/chem.200500704.
Texto completo da fonteDas, 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.º 33 (2011): 8377. http://dx.doi.org/10.1039/c1dt10609k.
Texto completo da fonteTeses / dissertações sobre o assunto "Benzoquinonemonoimine"
Torres, Ruiz Angelina. "Vers de nouveaux détecteurs des ions cyanures". Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0587.
Texto completo da fonteAs 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