Search Results - "Papke, Martin"

Synthesis, Electronic Properties and OLED Devices of Chromophores Based on λ5‐Phosphinines by Pfeifer, Gregor, Chahdoura, Faouzi, Papke, Martin, Weber, Manuela, Szűcs, Rózsa, Geffroy, Bernard, Tondelier, Denis, Nyulászi, László, Hissler, Muriel, Müller, Christian

“…A new series of 2,4,6‐triaryl‐λ5‐phosphinines have been synthesized that contain different substituents both on the carbon backbone and the phosphorus atom of…”
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Chemoselective Post‐Synthesis Modification of Pyridyl‐Substituted, Aromatic Phosphorus Heterocycles: Cationic Ligands for Coordination Chemistry by Dettling, Lea, Papke, Martin, Ernst, Moritz J., Weber, Manuela, Müller, Christian

“…Triazaphospholes are potential polydentate ligands due to the presence of both phosphorus and nitrogen donor atoms within the aromatic 5‐membered heterocycle…”
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Cover Feature: Pyridyl‐Functionalized 1‐Phosphabarrelene: Synthesis, Coordination Chemistry and Photochemical di‐π‐Methane Rearrangement (Chem. Eur. J. 63/2019) by Bruce, Marlene, Papke, Martin, Ehlers, Andreas W., Weber, Manuela, Lentz, Dieter, Mézailles, Nicolas, Slootweg, J. Chris, Müller, Christian

“…Di‐π‐methane rearrangement in a phosphorus compound The present manuscript reports on the synthesis of the first pyridyl‐functionalized 1‐phosphabarrelene from…”
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Pyridyl‐Functionalized 1‐Phosphabarrelene: Synthesis, Coordination Chemistry and Photochemical di‐π‐Methane Rearrangement by Bruce, Marlene, Papke, Martin, Ehlers, Andreas W., Weber, Manuela, Lentz, Dieter, Mézailles, Nicolas, Slootweg, J. Chris, Müller, Christian

“…The [4+2] cycloaddition of 2‐(2′‐pyridyl)‐4,6‐diphenyl‐λ3‐phosphinine with the highly reactive dienophile hexafluoro‐2‐butyne has been studied and the first…”
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Synthesis, Electronic Properties and OLED Devices of Chromophores Based on λ 5 -Phosphinines by Pfeifer, Gregor, Chahdoura, Faouzi, Papke, Martin, Weber, Manuela, Szűcs, Rózsa, Geffroy, Bernard, Tondelier, Denis, Nyulászi, László, Hissler, Muriel, Müller, Christian

“…A new series of 2,4,6-triaryl-λ -phosphinines have been synthesized that contain different substituents both on the carbon backbone and the phosphorus atom of…”
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Triazaphospholenium Tetrafluoroborate: A Phosphorus Analogue of a 1,2,3‐Triazole‐Derived Carbene by Papke, Martin, Dettling, Lea, Sklorz, Julian A. W., Szieberth, Dénes, Nyulászi, László, Müller, Christian

“…3H‐1,2,3,4‐Triazaphosphole derivatives can be selectively alkylated with Meerwein's reagent at the most nucleophilic nitrogen atom. According to the principle…”
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Frontispiece: Triazaphospholenium Tetrafluoroborate: A Phosphorus Analogue of a 1,2,3‐Triazole‐Derived Carbene by Papke, Martin, Dettling, Lea, Sklorz, Julian A. W., Szieberth, Dénes, Nyulászi, László, Müller, Christian

“…Heterocycles L. Nyulászi, C. Müller et al. describe the first formal phosphorus analogue of mesoionic carbenes in their Communication on page 16484. First…”
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Clicking the Arsenic-Carbon Triple Bond: An Entry into a New Class of Arsenic Heterocycles by Pfeifer, Gregor, Papke, Martin, Frost, Daniel, Sklorz, Julian A. W., Habicht, Marija, Müller, Christian

“…Arsaalkynes can undergo regioselective and quantitative [3+2] cycloaddition reactions with organic azides to give hitherto unknown 3H‐1,2,3,4‐triazaarsole…”
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Frontispiece: Clicking the Arsenic-Carbon Triple Bond: An Entry into a New Class of Arsenic Heterocycles by Pfeifer, Gregor, Papke, Martin, Frost, Daniel, Sklorz, Julian A. W., Habicht, Marija, Müller, Christian

“…Arsenic Heterocycles In their Communication on page 11760 ff. C. Müller et al. report a hitherto unknown triazaarsole. The synthesis was accomplished through a…”
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Triazaphospholenium‐tetrafluoroborat: das Phosphoranalogon eines von 1,2,3‐Triazol abgeleiteten Carbens by Papke, Martin, Dettling, Lea, Sklorz, Julian A. W., Szieberth, Dénes, Nyulászi, László, Müller, Christian

“…3H‐1,2,3,4‐Triazaphosphole können selektiv mit dem Meerwein‐Reagens am nukleophilsten Stickstoffatom alkyliert werden. Nach dem Konzept der Valenzisoelektronie…”
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Frontispiz: Triazaphospholenium‐tetrafluoroborat: das Phosphoranalogon eines von 1,2,3‐Triazol abgeleiteten Carbens by Papke, Martin, Dettling, Lea, Sklorz, Julian A. W., Szieberth, Dénes, Nyulászi, László, Müller, Christian

“…Heterocyclen L. Nyulászi, C. Müller et al. berichten in der Zuschrift auf S. 16706 über das erste formale Phosphoranalogon eines mesoionischen Carbens. Erste…”
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Frontispiz: Klick‐Reaktion an der Arsen‐Kohlenstoff‐Dreifachbindung: Zugang zu einer neuen Klasse arsenhaltiger Heterocyclen by Pfeifer, Gregor, Papke, Martin, Frost, Daniel, Sklorz, Julian A. W., Habicht, Marija, Müller, Christian

“…Arsenhaltige Heterocyclen C. Müller et al. beschreiben in der Zuschrift auf S. 11934 ff. ein bisher unbekanntes Triazaarsol. Die Synthese gelang durch…”
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Klick‐Reaktion an der Arsen‐Kohlenstoff‐Dreifachbindung: Zugang zu einer neuen Klasse arsenhaltiger Heterocyclen by Pfeifer, Gregor, Papke, Martin, Frost, Daniel, Sklorz, Julian A. W., Habicht, Marija, Müller, Christian

“…Arsaalkine gehen regioselektive und quantitative [3+2]‐Cycloadditionen mit organischen Aziden ein und bilden zuvor unbekannte 3H‐1,2,3,4‐Triazaarsolderivate…”
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Frontispiz: Klick-Reaktion an der Arsen-Kohlenstoff-Dreifachbindung: Zugang zu einer neuen Klasse arsenhaltiger Heterocyclen by Pfeifer, Gregor, Papke, Martin, Frost, Daniel, Sklorz, Julian A W, Habicht, Marija, Muller, Christian

“…Arsenhaltige Heterocyclen C. Muller etal. beschreiben in der Zuschrift auf S.11934ff. ein bisher unbekanntes Triazaarsol. Die Synthese gelang durch…”
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Frontispiz: Klick-Reaktion an der Arsen-Kohlenstoff-Dreifachbindung: Zugang zu einer neuen Klasse arsenhaltiger Heterocyclen by Pfeifer, Gregor, Papke, Martin, Frost, Daniel, Sklorz, Julian A. W., Habicht, Marija, Müller, Christian

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Klick-Reaktion an der Arsen-Kohlenstoff-Dreifachbindung: Zugang zu einer neuen Klasse arsenhaltiger Heterocyclen by Pfeifer, Gregor, Papke, Martin, Frost, Daniel, Sklorz, Julian A. W., Habicht, Marija, Müller, Christian

“…Arsaalkine gehen regioselektive und quantitative [3+2]-Cycloadditionen mit organischen Aziden ein und bilden zuvor unbekannte 3H-1,2,3,4-Triazaarsolderivate…”
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