Issue 29, 2019

Versatile coordinating abilities of acyclic N4 and N2P2 ligand frameworks in conjunction with Sn[N(SiMe3)2]2

Abstract

The adaptability of three acyclic tetradentate ligands with the –CHR–CHR– (R = H or alkyl substituent) linker in the backbone: bis(α-iminopyridine) L1 and the reduced form L2 and diaminodiphosphine L3 to stabilize various stannylenes has been explored. The reaction of L1 with two equivalents of Sn[N(SiMe3)2]2 led to the stabilization of a bisstannylene 1 through the ene-amide transformation of L1. The reaction of bisstannylene 1 with B(C6F5)3 and silver trifluoromethane sulfonate led to the formation of ligand stabilized Sn(II) dications 2 and 3 respectively. A mixture of Sn(II) dication 3 and a Sn(II) monocation 4 has been obtained from the reaction between 1 and trimethylsilyl trifluoromethane sulfonate. A 1 : 1 stoichiometric reaction between L3 and Sn[N(SiMe3)2]2 led to the isolation of a dimeric monostannylene 5 having a step-like structure with a Sn2N2 central ring. The reaction of L2 with Sn[N(SiMe3)2]2 underwent an electron transfer reaction ultimately leading to bis(α-iminopyridine) isolation.

Graphical abstract: Versatile coordinating abilities of acyclic N4 and N2P2 ligand frameworks in conjunction with Sn[N(SiMe3)2]2

Supplementary files

Article information

Article type
Paper
Submitted
11 fev 2019
Accepted
28 may 2019
First published
04 iyn 2019

Dalton Trans., 2019,48, 10953-10961

Versatile coordinating abilities of acyclic N4 and N2P2 ligand frameworks in conjunction with Sn[N(SiMe3)2]2

R. K. Raut, P. Sahoo, D. Chimnapure and M. Majumdar, Dalton Trans., 2019, 48, 10953 DOI: 10.1039/C9DT00617F

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