Control of dual emission behaviour of μ-oxo-bridged Si(IV) corrole dimers by substituent bulkiness

18 April 2022, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

The μ-oxo-bridged dimer of Si(IV) corrole has been recently reported to exhibit dual emissive properties depending on the solvent-viscosity. Here we examined the control of the excited-state dynamics and dual emission by meso-aryl substituents. Less hindered 10-unsubstituted and 10-phenyl-5,15-bis(pentafluorophenyl)-Si(IV) corrole dimers and more hindered 5,15-bis(pentafluorophenyl)-10-(2,4,6-trimethoxy)phenyl-Si(IV) corrole dimer were newly prepared and characterised. Interestingly, their solid-state structures are different; parallel, anti-parallel or orthogonal. In contrast, the energy-minimized structures in the excited-state have been suggested to be parallel in all cases owing to the significant excimer-like stabilization. As a result, different emission behaviours and viscosity dependence were observed.

Keywords

porphyrinoid
Si complex
dual emission
viscosity dependence
solid-state structure

Supplementary materials

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Title
Electronic supplementary information for the manuscript titled Control of dual emission behaviour of μ-oxo-bridged Si(IV) corrole dimers by substituent bulkiness
Description
1H NMR, HR-MS, optical and electrochemical properties, as well as single-crystal structures and DFT optimized structures.
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