Synthesis and characterization of the first neutral hexacoordinated silole complexes
Abstract
The first neutral hexacoordinated silole complexes were synthesized. Substituent patterns govern coordination modes and influence delocalization within diketonato ligands, markedly affecting photophysical properties and enabling charge-transfer excitations. This structural tunability provides a strategy to modulate the electronic and photophysical behavior of silole-based complexes, expanding their potential applications.