Abstract
Mesoionic compounds are currently hugely popular in several fields such as organic chemistry, organometallic chemistry and homogeneous catalysis. A new class of mesoionic compounds are the mesoionic imines (MIIs). For MIIs based on a 1,2,3-triazole core, the synthetic strategy involves alkylation/arylation of the triazole-N3 atom and subsequent deprotonation to de-liver MIIs. We present here 5-amino-4-pyridyl-1,2,3-triazole as an alternative and versatile synthon for generating metallo-MIIs. In this approach, we make use of metallation at the N-pyridyl/N3-traizole chelating pocket (instead of quarternisation of N3-triazole) and subsequent deprotonation to generate highly versatile and tunable metallo-MIIs. These unprecedented metallo-MIIs contain a highly nucleophilic N-donor site, and a tunable electrophilic metal site within the same platform. Apart from displaying strong and directed H-bonding interactions like their “classical” MII analogues, the metallo-MIIs engage in aromatic C-F activation as well as meta-C-H activation reactions. Facile synthesis of homo and heterodincuelar complexes which contain a mixed coordinative saturation/unsaturation with these metallo-MICs is presented. Apart from the metallo-MICs we have also used 5-amino-4-pyridyl-1,2,3-triazole as a viable precursor to generate the first examples of amido-1,2,3-triazole complexes and the first example of a “normal” (and not mesoionic) 1,2,3-triazole based imine. Apart from a combination of synthetic chemistry, multinuclear NMR spectroscopy and single crystal X-ray diffraction, (TD)DFT calculations were also used to shed light on the electronic structure and the frontier orbital situation of these compounds. Our results thus establish metallo-MIIs as a versatile new class of mesoionic compounds that combine the modularity of click reactions, with the functionality of metal fragments to generate electronically ambivalent compounds with a huge potential in synthetic chemistry, catalysis and beyond.
Supplementary materials
Title
Synthetic, spectroscopic, crystallographic and DFT data
Description
Synthetic procedures, 1H and 13C NMR spectra, crystallographic details, details of DFT calculations
Actions