Data of B3 group for: "Determination of Accessibility and Spatial Distribution of Chiral Rh Diene Complexes Immobilized on SBA-15 via Phosphine‑based NMR Probe Molecules" (doi:10.18419/darus-3272)

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Document Description

Citation

Title:

Data of B3 group for: "Determination of Accessibility and Spatial Distribution of Chiral Rh Diene Complexes Immobilized on SBA-15 via Phosphine‑based NMR Probe Molecules"

Identification Number:

doi:10.18419/darus-3272

Distributor:

DaRUS

Date of Distribution:

2022-12-13

Version:

1

Bibliographic Citation:

Kirchhof, Manuel, 2022, "Data of B3 group for: "Determination of Accessibility and Spatial Distribution of Chiral Rh Diene Complexes Immobilized on SBA-15 via Phosphine‑based NMR Probe Molecules"", https://doi.org/10.18419/darus-3272, DaRUS, V1

Study Description

Citation

Title:

Data of B3 group for: "Determination of Accessibility and Spatial Distribution of Chiral Rh Diene Complexes Immobilized on SBA-15 via Phosphine‑based NMR Probe Molecules"

Identification Number:

doi:10.18419/darus-3272

Authoring Entity:

Kirchhof, Manuel (University of Stuttgart, Institute of Organic Chemistry)

Grant Number:

358283783 - SFB 1333

Distributor:

DaRUS

Access Authority:

Laschat, Sabine

Depositor:

Kirchhof, Manuel

Date of Deposit:

2022-11-22

Holdings Information:

https://doi.org/10.18419/darus-3272

Study Scope

Keywords:

Chemistry, Asymmetric Catalysis, Rhodium Catalysis, Diene Ligands, Confinement, Phosphine, Probe Molecules, NMR Spectroscopy

Topic Classification:

Heterogenous Catalysis

Abstract:

In this dataset HPLC (high performance liquid chromatography) chromatograms of the products of the rhodium-catalyzed 1,2-addition and NMR spectra of all prepared catalysts and catalysis products (NMR) are included. The described 1,2-addition product is an N-tosyl amide which was formed from the reaction of triphenylboroxine with an N-tosyl imine. The catalysts are the chiral Rh norbornadiene phosphine complexes [RhCl(L1)(P(Ad)2(n-Bu))] and [RhCl(L1)(PPh3)]. Furthermore, the NMR data of phosphine complexation experiments is deposited. This data was collected to screen for suitable phosphines for the later quantification of accessible Rh diene complexes on SBA-15 via solid state NMR. Crystallographic data was published in Cambridge Structural Database (CSD) of the Cambridge Crystallographic Data Centre (CCDC) as stated under related datasets. In this dataset additional data from the crystal structure of [RhCl(L1)(P(Ad)2(n-Bu))] is included (plotted structure, CIF file, PDB file, RES file and a DAT file with tables listing all the significant measuring parameters, bond angles, bond distances and atom coordinates).

Kind of Data:

experimental data

Methodology and Processing

Sources Statement

Data Access

Other Study Description Materials

Related Studies

Structure [RhCl(L1)(P(Ad)2(n-Bu))]: Carolin Rieg, Manuel Kirchhof, Katrin Gugeler, Ann-Katrin Beurer, Lukas Stein, Klaus Dirnberger, Wolfgang Frey, Johanna R. Bruckner, Yvonne Traa, Johannes Kästner, Sabine Ludwigs, Sabine Laschat, Michael Dyballa, CCDC 2195463: Experimental Crystal Structure Determination, 2022, DOI: <a href="https://doi.org/10.5517/ccdc.csd.cc2cpkd1">10.5517/ccdc.csd.cc2cpkd1</a>

Related Publications

Citation

Title:

Carolin Rieg, Manuel Kirchhof, Katrin Gugeler, Ann-Katrin Beurer, Lukas Stein, Klaus Dirnberger, Wolfgang Frey, Johanna R. Bruckner, Yvonne Traa, Johannes Kästner, Sabine Ludwigs, Sabine Laschat, Michael Dyballa. Determination of accessibility and spatial distribution of chiral Rh diene complexes immobilized on SBA-15 via phosphine-based solid-state NMR probe molecules. Catal. Sci. Technol. 2022, Advance Article.

Identification Number:

10.1039/d2cy01578a

Bibliographic Citation:

Carolin Rieg, Manuel Kirchhof, Katrin Gugeler, Ann-Katrin Beurer, Lukas Stein, Klaus Dirnberger, Wolfgang Frey, Johanna R. Bruckner, Yvonne Traa, Johannes Kästner, Sabine Ludwigs, Sabine Laschat, Michael Dyballa. Determination of accessibility and spatial distribution of chiral Rh diene complexes immobilized on SBA-15 via phosphine-based solid-state NMR probe molecules. Catal. Sci. Technol. 2022, Advance Article.

Other Study-Related Materials

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checkcif_report_s2867lm.pdf

Notes:

application/pdf

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plot_s2867_sq.docx

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application/vnd.openxmlformats-officedocument.wordprocessingml.document

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s2867lm_sq.cif

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chemical/x-cif

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s2867lm_sq.pdb

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chemical/x-pdb

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s2867lm_sq.res

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text/plain

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s2867tab.dat

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text/x-fixed-field

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Label:

1,2-Addition with [RhCl(L1)PPh3].xps

Notes:

application/vnd.ms-xpsdocument

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Additional NMR experiments.zip

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application/zip

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Phosphane screening.zip

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application/zip

Other Study-Related Materials

Label:

[RhCl(L1)PAd2(n-Bu)].zip

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application/zip

Other Study-Related Materials

Label:

[RhCl(L1)PPh3].zip

Notes:

application/zip