Issue 44, 2021

Hypercoordinated eka-tin materials with dangling aryl-methoxy and -methylthio ligands exhibiting intramolecular secondary bonding and aryl bond stabilization in reactions with organotin chlorides

Abstract

The syntheses of [2-(CH3ECH2)C6H4]PbPh3−nCln, (n = 0, E = O (4), E = S (5); n = 1, E = O (6), E = S (7); n = 2, E = O (8), are described. NMR and single crystal data illustrate significant Pb⋯E interactions increasing as n progresses from 0 to 2. The Pb⋯E interactions stabilize the Pb–aryl bonding to the extent that the reactions of 4 and 5 with Me2SnCl2 result in interchange of a Ph group and Cl to produce 6 and 7, respectively, together with Me2PhSnCl.

Graphical abstract: Hypercoordinated eka-tin materials with dangling aryl-methoxy and -methylthio ligands exhibiting intramolecular secondary bonding and aryl bond stabilization in reactions with organotin chlorides

Supplementary files

Article information

Article type
Paper
Submitted
26 Aug 2021
Accepted
13 Oct 2021
First published
13 Oct 2021

Dalton Trans., 2021,50, 16084-16091

Hypercoordinated eka-tin materials with dangling aryl-methoxy and -methylthio ligands exhibiting intramolecular secondary bonding and aryl bond stabilization in reactions with organotin chlorides

A. Ornelas, R. Arias-Ugarte, A. J. Metta-Magaña, H. K. Sharma and K. H. Pannell, Dalton Trans., 2021, 50, 16084 DOI: 10.1039/D1DT02781F

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