Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Sebastian Burck"'
Autor:
Martin Nieger, Sebastian Burck, Dietrich Gudat, Jason D. Masuda, Johannes Bender, Nick A. Giffin, Oliver Puntigam, Arthur D. Hendsbee, Fabian Ehret, Daniela Förster
Publikováno v:
European Journal of Inorganic Chemistry. 2013:2041-2050
Symmetrical N-heterocyclic 1,1′,3,3′-tetrahydro-2,2′-bi-1,3,2-diazaphospholes and 2,2′-bi-1,3,2-diazaphospholidines are prepared by time-saving, sequential “one-pot” syntheses starting from 1,4-diazabutadienes or N-alkyl or N-aryl-substit
Autor:
László Nyulászi, Basit Niaz, Oldamur Hollóczki, Mark Niemeyer, Joachim Heinicke, Sebastian Burck, Peter G. Jones, Dietrich Gudat, Bhaskar R. Aluri
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements. 186:683-687
Benzofused 1H-1,3-azaphospholes are lithiated at the N-atom by tBuLi but phosphinylation takes place at either the N- or the P-atom. Smaller chlorophosphines react at nitrogen, bulkier react at phosphorus. Substituents at C2 promote the latter mode.
Autor:
Martin Hofmann, Dietrich Gudat, László Nyulászi, Zoltán Benkő, Falk Lissner, Sebastian Burck, Ulrich Zenneck
Publikováno v:
Chemistry - A European Journal. 16:2857-2865
Computational studies on a series of polyphospholyl-substituted N-heterocyclic phosphines (CH) 2 (NR) 2 P-P n (CH) 5-n (R=Me, n=1-5) disclosed that increasing formal replacement of CH units in the phosphole ring by phosphorus atoms is associated with
Autor:
Peter G. Jones, Bhaskar R. Aluri, Sebastian Burck, Dietrich Gudat, Oldamur Hollóczki, Joachim Heinicke, László Nyulászi, Mark Niemeyer
Publikováno v:
Chemistry - A European Journal. 15:12263-12272
Synthetic and structural aspects of the phosphanylation of 1,3-benzazaphospholides 1(Li), ambident benzofused azaphosphacyclopentadienides, are presented. The unusual properties of phospholyl-1,3,2-diazaphospholes inspired us to study the coupling of
Autor:
Sander G. A. van Assema, J. Chris Slootweg, José M. Otero, Antonio L. Llamas-Saiz, Mark J. van Raaij, Mark Overhand, Bas Lastdrager, Koop Lammertsma, Sebastian Burck, Andreas W. Ehlers, Bruno Dacunha-Marinho
Publikováno v:
Chemistry: A European Journal, 15(33), 8134-45. Wiley-VCH Verlag
Burck, S, van Assema, S G A, Lastdrager, B, Slootweg, J C, Ehlers, A W, Otero, J M, Dacunha-Marinho, B, Llamas-Saiz, A L, Overhand, M, van Raaij, M J & Lammertsma, K 2009, ' Bisphosphine-functionalized cyclic decapeptides based on the natural product Gramicidin S: a potential scaffold for transition-metal coordination ', Chemistry: A European Journal, vol. 15, no. 33, pp. 8134-45 . https://doi.org/10.1002/chem.200901127
Burck, S, van Assema, S G A, Lastdrager, B, Slootweg, J C, Ehlers, A W, Otero, J M, Dacunha-Marinho, B, Llamas-Saiz, A L, Overhand, M, van Raaij, M J & Lammertsma, K 2009, ' Bisphosphine-functionalized cyclic decapeptides based on the natural product Gramicidin S: a potential scaffold for transition-metal coordination ', Chemistry: A European Journal, vol. 15, no. 33, pp. 8134-45 . https://doi.org/10.1002/chem.200901127
The natural product Gramicidin S is a promising scaffold for novel oligopeptide-based bisphosphine ligands, combining the advantageous rigid chiral backbone with the close proximity of phosphine substituents. The required unnatural, phosphine-contain
Publikováno v:
Organometallics. 28:1447-1452
A CC-saturated N-heterocyclic diphosphine was prepared and reacted with W(CO)4(cod) in acetonitrile to give a mixture of two complexes arising from insertion of an acetonitrile molecule or a metal ...
Autor:
Martin Nieger, László Nyulászi, Dietrich Gudat, Sebastian Burck, Zoltán Benkõ, Dénes Szieberth
Publikováno v:
Zeitschrift für anorganische und allgemeine Chemie. 635:245-252
P-bromo- and P-Iodo-substituted N-heterocyclic phosphanes (NHP) were synthesized by halogen exchange starting from the P-chloro compound and characterized by spectroscopic data and X-ray diffraction studies. Whereas the Br-NHP still forms a molecular
Publikováno v:
Zeitschrift für Naturforschung B. 64:63-72
The reactions of 1,1-diamino-2,2-diphenyl-substituted diphosphines featuring various degrees of P-P bond polarization with different alkynes were investigated. All diphosphines reacted with alkynes carrying one or two electron withdrawing carboxylic
Publikováno v:
European Journal of Inorganic Chemistry. 2008:704-707
Diphosphanes with polarised P–P bonds react readily with Lewis acids like borane, gallium trichloride, or with elemental selenium, to give products arising from electrophilic attack at the more basic phosphorus atom and consecutive bond cleavage. S
Autor:
Dietrich Gudat, Sebastian Burck
Publikováno v:
Inorganic Chemistry. 47:315-321
NMR studies of reactions between some N-heterocyclic and acyclic diamino phosphenium ions (R2N)2P+ and P-chlorophosphines (R2N)2PCl suggest that the reactants interact via chloride scrambling rather than by formation of P-P bonded phosphenium-phosphi