Abstract
The coordination behavior of a series of [Sn(OR)2] systems modified by substituted amine-bis(phenolate)ligands was investigated. The complexes were synthesised from the reaction of Sn[N(SiMe3)2]2 and the appropriate pro-ligand: N,N-bis(3,5-dimethyl-2-hydroxybenzyl)ethylamine (L1H2), N′,N‘-bis(2-hydroxy-3,5-dimethylbenzyl)-N,N-dimethylethylenediamine (L2H2), N,N‘-bis(3,5-dimethyl-2-hydroxyphenylmethyl)-N,N‘-dimethylethylenediamine (L3H2), 1,4-bis(2-hydroxy-3,5-dimethylbenzyl)-1,4-diazepane (L4H2), 2,2′,4,4′-tetramethyl-6,6′-piperazine-1,4-diylbis(methylene)-bisphenol (L5H2) and N′,N′,N′′,N′′-tetrakis(2-hydroxy-3,5-dimethylbenzyl)-1,2-ethanediamine, and the products were identified as follows: [{L1}Sn]2 (1), [{L2}Sn] (2), [{L3}Sn] (3), [{L4}Sn], (4) and [{L6}Sn2]·(Py)2 (5). Reaction of complex (1) with O2 results in the formation of the Sn(iv) species [{L1}2Sn] (6), the molecular structure of which was also determined.
| Original language | English |
|---|---|
| Pages (from-to) | 13632-13641 |
| Number of pages | 10 |
| Journal | Dalton Transactions |
| Volume | 54 |
| Issue number | 36 |
| Early online date | 7 Aug 2025 |
| DOIs | |
| Publication status | Published - 28 Sept 2025 |
Data Availability Statement
The data that support the findings of this study are available in the SI of this article. General experimental details, the synthesis of [tBu4Sn] and crystallographic data for [tBu4Sn]; experimental details of the data collection/X-ray crystallographic studies of 1–6 and [tBu4Sn]; and characterisation data for the {tBu} analogue of 3, tBu4Sn. See DOI: https://doi.org/10.1039/d5dt01442e.CCDC 2465589–2465595 contain the supplementary crystallographic data for this paper.66a–g
Where possible, additional data that support the findings of this study are available from the corresponding authors upon reasonable request.
ASJC Scopus subject areas
- Inorganic Chemistry