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Kerber RN, Kerber T, Rozanska X, et al. Grafting trimethylaluminum and its halogen derivatives on silica: general trends for (27)Al SS-NMR response from first principles calculations. Phys Chem Chem Phys. 2015;17(40):26937-45doi: 10.1039/c5cp04109k.
Kerber, R. N., Kerber, T., Rozanska, X., Delbecq, F., & Sautet, P. (2015). Grafting trimethylaluminum and its halogen derivatives on silica: general trends for (27)Al SS-NMR response from first principles calculations. Physical chemistry chemical physics : PCCP, 17(40), 26937-45. https://doi.org/10.1039/c5cp04109k
Kerber, Rachel Nathaniel, et al. "Grafting trimethylaluminum and its halogen derivatives on silica: general trends for (27)Al SS-NMR response from first principles calculations." Physical chemistry chemical physics : PCCP vol. 17,40 (2015): 26937-45. doi: https://doi.org/10.1039/c5cp04109k
Kerber RN, Kerber T, Rozanska X, Delbecq F, Sautet P. Grafting trimethylaluminum and its halogen derivatives on silica: general trends for (27)Al SS-NMR response from first principles calculations. Phys Chem Chem Phys. 2015 Oct 28;17(40):26937-45. doi: 10.1039/c5cp04109k. PMID: 26403260.
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Phys Chem Chem Phys. 2015 Oct 28;17(40):26937-45. doi: 10.1039/c5cp04109k.

Grafting trimethylaluminum and its halogen derivatives on silica: general trends for (27)Al SS-NMR response from first principles calculations.

Physical chemistry chemical physics : PCCP

Rachel Nathaniel Kerber, Torsten Kerber, Xavier Rozanska, Françoise Delbecq, Philippe Sautet

Affiliations

  1. Université de Lyon, CNRS, Institut de Chimie de Lyon, Ecole Normale Supérieure de Lyon, 46 allée d'Italie, F-69364 Lyon Cedex 07, France. [email protected].

PMID: 26403260 DOI: 10.1039/c5cp04109k

Abstract

(27)Al NMR is the method of choice for studying grafted Al species on a large area solid support, such as co-catalysts for α-olefin oligomerization involving mesoporous silica materials. Here, we show how to interpret the (27)Al solid-state NMR spectrum and parameters for various types of Al monomeric and dimeric alkyl and halogen compounds grafted on silica, based on the trends obtained from first-principles calculations. Since most alkylaluminum species tend to form dimers in the gas phase, we chose as prototypes both the AlMe3 monomer and the Al2Me6 dimer. On top of that the influence of chlorine substituents on the NMR parameters is explored considering all possible isomers. There are two main effects on the Al NMR parameters observed in the case of monomers: (i) the larger π-donating character of the ligands (from Me to Cl for example) leads to a decrease of the quadrupolar coupling constant CQ and (ii) the larger σ-attracting character of the ligand (from Cl to F for example) yields an upfield variation of the Al chemical shift δISO while in contrast CQ is increased. The same is true also in the case of dimeric species, with an additional specific effect. By (27)Al solid state NMR we can differentiate clearly between terminal and bridge positions for the substituents. The reason for this phenomenon is explained in terms of different natural localized MO (NLMO) contributions to the CQ parameter. This aspect is important because the surface sites for this type of system are expected to be mostly dinuclear Al species, grafted on the silica surface via either two terminal or two bridging siloxy ligands.

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