Catalysis Data and NMR Characterization of all Compounds for "Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions"doi:10.18419/darus-1250DaRUS2021-04-191Kirchhof, Manuel, 2021, "Catalysis Data and NMR Characterization of all Compounds for "Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions"", https://doi.org/10.18419/darus-1250, DaRUS, V1Catalysis Data and NMR Characterization of all Compounds for "Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions"doi:10.18419/darus-1250Kirchhof, Manuel358283783 - SFB 1333DaRUSLaschat, SabineKirchhof, Manuel2021-01-22Chemistry1,4-AdditionMonomerX-ray Absorption SpectroscopyRhodium Catalysis1,2-AdditionDimerTheoretical CalculationsIn this dataset HPLC (high performance liquid chromatography) chromatograms of the products of the rhodium-catalyzed 1,2-addition and the respective examinations of the nonlinear and nonlinear-like effect (HPLC 1.2-Addition; HPLC-Messungen NLE und NLLE) and gas chromatograms of the products of the rhodium-catalyzed 1,4-addition (GC-Analytik) are listed. Furthermore the NMR spectra of all prepared catalysts and catalysis products (NMR Analytik Verbindungen) are included.Experimental DataM. Kirchhof, K. Gugeler, F. R. Fischer, M. Nowakowski, A. Bauer, S. Alvarez-Barcia, K. Abitaev, M. Schnierle, Y. Qawasmi, W. Frey, A. Baro, D. P. Estes, T. Sottmann, M. R. Ringenberg, B. Plietker, M. Bauer, J. Kästner, S. Laschat, Organometallics 2020, 39, 3131-3145.10.1021/acs.organomet.0c00310M. Kirchhof, K. Gugeler, F. R. Fischer, M. Nowakowski, A. Bauer, S. Alvarez-Barcia, K. Abitaev, M. Schnierle, Y. Qawasmi, W. Frey, A. Baro, D. P. Estes, T. Sottmann, M. R. Ringenberg, B. Plietker, M. Bauer, J. Kästner, S. Laschat, Organometallics 2020, 39, 3131-3145.8a.zipapplication/zip8b.zipapplication/zip1,2-Addition Dioxane [(Rh(1))2Cl]SbF6.xpsapplication/vnd.ms-xpsdocument1,2-Addition Dioxane [RhCl(1)]2.xpsapplication/vnd.ms-xpsdocument1,2-Addition Dioxane [RhCl(2)].xpsapplication/vnd.ms-xpsdocument1,2-Addition Dioxane [RhCl(ent-1)]2.xpsapplication/vnd.ms-xpsdocument1,2-Addition Dioxane [RhOH2(2)]SbF6.xpsapplication/vnd.ms-xpsdocument1,2-Addition ME [(Rh(1))2Cl]SbF6.xpsapplication/vnd.ms-xpsdocument1,2-Addition ME [RhCl(1)].xpsapplication/vnd.ms-xpsdocument1,2-Addition ME [RhCl(1)]2.xpsapplication/vnd.ms-xpsdocument1,2-Addition ME [RhCl(ent-1)]2 in situ.xpsapplication/vnd.ms-xpsdocument1,2-Addition ME [RhCl(ent-1)]2.xpsapplication/vnd.ms-xpsdocument1,2-Addition ME [RhOH2(2)]SbF6.xpsapplication/vnd.ms-xpsdocument1,2-Addition Racemate.xpsapplication/vnd.ms-xpsdocumentKomplexe NLE.zipapplication/zipLiganden NLE.zipapplication/zipLiganden NLLE.zipapplication/zip5.zipapplication/zip8a.zipapplication/zip8b.zipapplication/zip9.zipapplication/zipent-1.zipapplication/zipepi-1.zipapplication/zip[(Rh(1))2Cl]SbF6.zipapplication/zip[RhCl(1)]2.zipapplication/zip[RhCl(2)].zipapplication/zip[RhCl(ent-1)]2.zipapplication/zip[RhOH2(2)]SbF6.zipapplication/zip