N-Heterocyclic Silylene-Copper(I)-Aryl Complex: Multitasking Cu(I) Synthon

02 July 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

In this work, we have prepared [PhC{N(tBu)}2SiN(SiMe3)2] (1) coordinated organocopper(I) complexes (2 and 3) and utilized them as a useful synthon for the aryl group transfer and cleavage of a variety of homolytic and heterolytic bonds. Complex 2 was used as a mesityl transfer reagent in the C–C cross-coupling reaction that led to the formation of the coupled products in excellent yields. Further, we have demonstrated the reaction of 2 with compounds having B–B and Se–Se bonds, which led to the formation of dimeric µ-boryl bound Cu(I) complex (6) and a new class of unprecedented NHSi-supported copper-selenides (8 and 9). Finally, this new synthetic methodology smoothly afforded several elusive NHSi-copper amide complexes (10-14).

Keywords

N-Heterocyclic silylene
coinage metal complexes
organo-copper complexes
C-C coupling
copper amide

Supplementary materials

Title
Description
Actions
Title
N-Heterocyclic Silylene-Copper(I)-Aryl Complex: Multitasking Cu(I) Synthon
Description
S1. Experimental Section S1.1. Synthesis of Complexes 2-14, S1 S1.2. C-C Cross-Coupling Reactions S2.1. NMR Spectra of Complexes 2-14, S1 S2.2. NMR Spectra of C-C Coupled Products S3. Crystallographic Details of Complexes 2-14, S1 S4. Molecular Structure of Complex 5, 7 and 10 S5. Packing of Complex 5 and 12 through Various Non-covalent Interactions S6. Hirshfield Analysis of Complex 5 S7. Quantum Chemical Calculations
Actions

Comments

Comments are not moderated before they are posted, but they can be removed by the site moderators if they are found to be in contravention of our Commenting Policy [opens in a new tab] - please read this policy before you post. Comments should be used for scholarly discussion of the content in question. You can find more information about how to use the commenting feature here [opens in a new tab] .
This site is protected by reCAPTCHA and the Google Privacy Policy [opens in a new tab] and Terms of Service [opens in a new tab] apply.