Advancement of the chemistry of organotin–Schiff base complexes: a crystallographic perspective

Abstract

This comprehensive review delves into the intricate realm of organotin complexes with Schiff base ligands, offering a detailed analysis of their structural characteristics and coordination behaviour. The study meticulously compiles and critically evaluates organotin complexes that have undergone structural elucidation via the powerful technique of X-ray crystallography, providing a robust foundation for understanding their three-dimensional architectures and bonding motifs. A central focus is directed towards the coordination versatility exhibited by Schiff bases derived from a diverse array of precursors, including amino acids, hydrazines, hydrazones, dihydrazones, and amino alcohols, which showcase their remarkable ability to engage with tin centres in multifaceted ways, supporting a spectrum of coordination geometries and oxidation states. Aliphatic and aromatic Schiff bases are explored extensively, revealing their propensity to form diverse additives and chelates with varying stoichiometries and coordination mechanisms, existing in both neutral and deprotonated forms.

Graphical abstract: Advancement of the chemistry of organotin–Schiff base complexes: a crystallographic perspective

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Perspective
Submitted
06 May 2025
Accepted
11 Jun 2025
First published
12 Jun 2025

Dalton Trans., 2025, Advance Article

Advancement of the chemistry of organotin–Schiff base complexes: a crystallographic perspective

R. Joshi, Dalton Trans., 2025, Advance Article , DOI: 10.1039/D5DT01063B

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