Issue 36, 2018

Alkali metal complexes as efficient catalysts for hydroboration and cyanosilylation of carbonyl compounds

Abstract

We report here reactions between the N-adamantyliminopyrolyl ligand 2-(AdN[double bond, length as m-dash]CH)–C4H3NH (L–H) and alkali metal hexamethyldisilazides [MN(SiMe3)2] (M = Li, Na and K) to afford the dimeric [{2-(AdN[double bond, length as m-dash]CH)–C4H3NLi(THF)}2] (1), [{2-(AdN[double bond, length as m-dash]CH)–C4H3N}{Na(THF)1.5}2] (2) and polymeric [{2-(AdN[double bond, length as m-dash]CH)–C4H3NK(THF)}n] (3) complexes at ambient temperature. A one-pot reaction between L–H, [KN(SiMe3)2] and alkaline earth metal diiodide (AeI2) in a 2 : 2 : 1 molar ratio, which resulted in the formation of a heteroleptic Ae metal complex [κ2-{2-(AdN[double bond, length as m-dash]CH)–C4H3N}2Ae(THF)2] [Ae = Mg (4), Ca (5)], is also reported. The solid-state structures of complexes 1, 3 and 4 were established through single-crystal X-ray diffraction analysis. The alkali and alkaline earth metal complexes 1–5 were utilised as precatalysts for the catalytic hydroboration of pinacolborane (HBpin) with aldehydes and ketones, and potassium complex 3 was identified as a competent catalyst under mild conditions. Additionally, cyanosilylation of carbonyl compounds was explored with trimethylsilyl cyanide and aldehydes/ketones, using the alkali metal precatalyst 3 under mild conditions. In both catalytic processes, the potassium catalyst 3 exhibited high tolerance towards a number of functional groups.

Graphical abstract: Alkali metal complexes as efficient catalysts for hydroboration and cyanosilylation of carbonyl compounds

Supplementary files

Article information

Article type
Paper
Submitted
18 Maijs 2018
Accepted
16 Jūl. 2018
First published
17 Jūl. 2018

Dalton Trans., 2018,47, 12613-12622

Alkali metal complexes as efficient catalysts for hydroboration and cyanosilylation of carbonyl compounds

A. Harinath, J. Bhattacharjee, H. P. Nayek and T. K. Panda, Dalton Trans., 2018, 47, 12613 DOI: 10.1039/C8DT02032A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements