Importance of co-donor field strength in the preparation of tetradentate α-diimine nickel hydrosilylation catalysts

Tyler M. Porter; Gabriel B. Hall; Thomas L. Groy; Ryan Trovitch

doi:10.1039/c3dt52419a

Importance of co-donor field strength in the preparation of tetradentate α-diimine nickel hydrosilylation catalysts

Tyler M. Porter, Gabriel B. Hall, Thomas L. Groy, Ryan Trovitch

CLAS-NS: Molecular Sciences, School of (SMS)

Research output: Contribution to journal › Article › peer-review

21 Scopus citations

Abstract

Although bis(α-diimine)Ni complexes were prepared when amine-substituted chelates were added to Ni(COD)₂, the incorporation of strong-field phosphine donors allowed the isolation of (κ⁴- N,N,P,P-DI)Ni hydrosilylation catalysts. The crystallographic investigation of two different (κ⁴-N,N,P,P-DI)Ni compounds revealed that the geometry about nickel influences the observed degree of α-diimine reduction.

Original language	English (US)
Pages (from-to)	14689-14692
Number of pages	4
Journal	Dalton Transactions
Volume	42
Issue number	41
DOIs	https://doi.org/10.1039/c3dt52419a
State	Published - Nov 7 2013

ASJC Scopus subject areas

Inorganic Chemistry

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abstract = "Although bis(α-diimine)Ni complexes were prepared when amine-substituted chelates were added to Ni(COD)2, the incorporation of strong-field phosphine donors allowed the isolation of (κ4- N,N,P,P-DI)Ni hydrosilylation catalysts. The crystallographic investigation of two different (κ4-N,N,P,P-DI)Ni compounds revealed that the geometry about nickel influences the observed degree of α-diimine reduction.",

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AU - Hall, Gabriel B.

AU - Groy, Thomas L.

AU - Trovitch, Ryan

PY - 2013/11/7

Y1 - 2013/11/7

N2 - Although bis(α-diimine)Ni complexes were prepared when amine-substituted chelates were added to Ni(COD)2, the incorporation of strong-field phosphine donors allowed the isolation of (κ4- N,N,P,P-DI)Ni hydrosilylation catalysts. The crystallographic investigation of two different (κ4-N,N,P,P-DI)Ni compounds revealed that the geometry about nickel influences the observed degree of α-diimine reduction.

AB - Although bis(α-diimine)Ni complexes were prepared when amine-substituted chelates were added to Ni(COD)2, the incorporation of strong-field phosphine donors allowed the isolation of (κ4- N,N,P,P-DI)Ni hydrosilylation catalysts. The crystallographic investigation of two different (κ4-N,N,P,P-DI)Ni compounds revealed that the geometry about nickel influences the observed degree of α-diimine reduction.

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