Search results for "Phosphane"
showing 10 items of 79 documents
CCDC 1578509: Experimental Crystal Structure Determination
2018
Related Article: Florian Chotard, Raluca Malacea-Kabbara, Cédric Balan, Ewen Bodio, Michel Picquet, Philippe Richard, Miguel Ponce-Vargas, Paul Fleurat-Lessard, Pierre Le Gendre|2018|Organometallics|37|812|doi:10.1021/acs.organomet.7b00851
CCDC 827095: Experimental Crystal Structure Determination
2012
Related Article: P.Farras, F.Teixidor, I.Rojo, R.Kiveks, R.Sillanpaa, P.Gonzalez-Cardoso, C.Vinas|2011|J.Am.Chem.Soc.|133|16537|doi:10.1021/ja205850p
CCDC 1532063: Experimental Crystal Structure Determination
2017
Related Article: Benedict Kemper, Maximilian von Gröning, Vanessa Lewe, Daniel Spitzer, Tobias Otremba, Natascha Stergiou, Dieter Schollmeyer, Edgar Schmitt, Bart Jan Ravoo, Pol Besenius|2017|Chem.-Eur.J.|23|6048|doi:10.1002/chem.201700588
CCDC 1978440: Experimental Crystal Structure Determination
2020
Related Article: Sarah Keller, Alessandro Prescimone, Maria-Grazia La Placa, José M. Junquera-Hernández, Henk J. Bolink, Edwin C. Constable, Michele Sessolo, Enrique Ortí, Catherine E. Housecroft|2020|RSC Advances|10|22631|doi:10.1039/D0RA03824E
CCDC 2193619: Experimental Crystal Structure Determination
2022
Related Article: Araceli de Aquino, Jas S. Ward, Kari Rissanen, Gabriel Aullón, João Carlos Lima, Laura Rodríguez|2022|Inorg.Chem.|61|20931|doi:10.1021/acs.inorgchem.2c03351
A Discrete P⋅⋅⋅II⋅⋅⋅P Assembly: The Large Influence of Weak Interactions on the31P NMR Spectra of Phosphane–Diiodine Complexes
2006
Thioethers, except derivatives of [7-R-7,8-C2B9H11] , are more weakly coordinating ligands than phosphanes. This difference is evidenced by the I I distances in the spokeshaped charge-transfer (CT) complexes R2S·I2 and R3P·I2 (Figure 1). The I I distance is sensitive to the strength of the interaction between the s* LUMO orbital on I2 and the HOMO orbital of the donor atom: the stronger the donor, the longer the I I distance. In these spoke CT complexes, the I I distance varies from 3.2 0.2 7 in R3P·I2 adducts [5] to 2.80 0.05 7 in R2S·I2 adducts, [6] indicating the weaker donor character of the thioether group. Whereas extended I2 arrays, spoke adducts of I2, polyiodides, and other structu…
Synthesis and reactivity of P-ferrocenylalkylidenephosphanes and related iminophosphanes and diphosphenes
1997
P-Ferrocenyl-substituted alkylidenephosphanes have been prepared and characterized spectroscopically. Their ready conversion to the corresponding acylphosphanes and 1,2-diacyldiphosphanes, as well as a new type of phosphirene synthesis are presented. The X-ray structure of the tetraferrocenyl-substituted diacyldiphosphane has been investigated. Furthermore, P-ferrocenyl iminophosphanes and their complexation behaviour are described. Diferrocenyldiphosphene, which is known to be unstable, has been stabilized by complexation; this has been confirmed by NMR-spectroscopy and X-ray structure analysis.
CCDC 142589: Experimental Crystal Structure Determination
2001
Related Article: T.Grob, G.Seybert, W.Massa, F.Weller, R.Palaniswami, A.Greiner, K.Dehnicke|2000|Angew.Chem.,Int.Ed.|39|4373|doi:10.1002/1521-3773(20001201)39:23<4373::AID-ANIE4373>3.0.CO;2-K
CCDC 1824417: Experimental Crystal Structure Determination
2020
Related Article: Lucia Volbach, Niklas Struch, Fabian Bohle, Filip Topić, Gregor Schnakenburg, Andreas Schneider, Kari Rissanen, Stefan Grimme, Arne Lützen|2020|Chem.-Eur.J.|26|3335|doi:10.1002/chem.201905070
ChemInform Abstract: A Versatile Palladium/Triphosphane System for Direct Arylation of Heteroarenes with Chloroarenes at Low Catalyst Loading.
2010
The present new catalyst system can be used for the direct arylation of various heteroaromatic compounds at low palladium loadings.